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DTSTART;TZID=America/New_York:20190918T083000
DTEND;TZID=America/New_York:20190918T133000
DTSTAMP:20260611T070626
CREATED:20190906T180331Z
LAST-MODIFIED:20190919T155451Z
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SUMMARY:Webinar: Expert Perspectives on Attaining Publishable Western Blot Data
DESCRIPTION:Publishing your Western blot data isn’t easy\, and sometimes a little guidance would be nice. That’s why LI-COR has teamed up with these experts to get you the very best intel on publishing your research. \nDiscover what publishers expect\, reviewers want\, and LI-COR is doing to help you get there with our “Expert Perspectives on Attaining Publishable Western Blot Data” webinar on September 18th at 8:30 am and 1:30 pm CDT. \n  \nSpeakers:\n  \n\nDr. Kaoru Sakabe\nData Integrity Manager at the American Society for Biochemistry and Molecular Biology (ASBMB) \n  \n\nDr. Matthew K. Summers\nAssociate Professor at the Ohio State University Comprehensive Cancer Center \n\n  \n\nJeff Harford\nSenior Product Manager\, Biotechnology at LI-COR Biosciences \n\n  \nRegister Here
URL:https://resources.govsci.com/event/expert-perspectives-on-attaining-publishable-western-blot-data/
LOCATION:From your desktop or mobile device
CATEGORIES:Webinar
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20190815T110000
DTEND;TZID=America/New_York:20190815T120000
DTSTAMP:20260611T070626
CREATED:20190729T131419Z
LAST-MODIFIED:20190919T155653Z
UID:7210-1565866800-1565870400@resources.govsci.com
SUMMARY:Webinar: Real-Time Analysis of Cellular Phagocytosis; Characterization of Anti-CD47 Antibodies as Potential Novel Immuno-Therapies
DESCRIPTION:August 15\, 2019 at 8am PDT / 11am EDT / 4pm BST / 5pm CEST\nAlongside intense efforts to exploit T-cells as immunotherapies for cancer (e.g. checkpoint inhibitors\, CAR-T\, T-cell metabolism)\, researchers are increasingly considering other immune cell types for novel targets. One example is the enhancement of macrophage function via inhibitors of CD47 “don’t-eat-me” signaling proteins\, enabling tumor cells to evade clearance by neighbouring phagocytes (Kim et al\, 2012\, Leukemia 26\, 2538–2545). In order to identify new CD47 and phagocyte modulators\, novel\, direct and validated assays with throughput commensurate to drug discovery are required. Watch this webinar to learn how: \n\nReal-time live-cell analysis using pH-sensitive fluorescent probe-labeled target cells can be used to visualize and quantify phagocytosis.\nYou can share data on the pro-phagocytic effects of anti-CD47 antibodies.\nOther live-cell phenotypic assays (e.g. apoptosis\, proliferation) are used to validate mechanisms of action.\n\nCertificate of attendance All webinar participants can download a certificate of attendance\, with a learning outcomes summary document for continuing education purposes. \n\nPresenters\n\n\n\n\n\n\nDr. Tim Dale\nHead of BioAnalytics Applications Sartorius Corporation Sartorius\n\n\nTim co-founded the European laboratories of Essen BioScience in 2009 and is Head of BioAnalytics Applications\, Sartorius Corporation\, managing R&D operations.  A highly experienced industrial pharmacologist and leader with more than 20 years of service\, Tim has a track record in applied drug discovery.  Applying his knowledge and expertise to drug discovery programs in the neurology\, psychiatry and gastrointestinal therapeutic areas\, he has contributed to the progression of a number of candidate molecules into clinical studies.  Tim has co-authored over 20 publications and patents relating to pharmacology\, ion channels and cell-based assays.  Most recently\, Tim is applying his many years of experience to extend the portfolio of cell-based applications utilising live-cell analysis in the fields of oncology\, immunology and neuroscience.\n\n\n\n\n\n\n\nDr Lois Manton-O’Byrne\nEditor SelectScience\n\n\n\nDr Lois Manton-O’Byrne is the Editor of SelectScience. Lois plays an integral role in shaping the content of the SelectScience communities\, particularly chemistry and applied science\, and engaging with scientists. She studied chemistry at the University of St Andrews\, and later achieved a PhD from the University of Bath\, focusing on sustainable plastics.\n\nRegister Here
URL:https://resources.govsci.com/event/real-time-analysis-of-cellular-phagocytosis-characterization-of-anti-cd47-antibodies-as-potential-novel-immuno-therapies/
LOCATION:From your desktop or mobile device
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/png:https://resources.govsci.com/wp-content/uploads/2019/07/Essen_logo.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20190717T113000
DTEND;TZID=America/New_York:20190717T123000
DTSTAMP:20260611T070626
CREATED:20190717T125201Z
LAST-MODIFIED:20190919T160420Z
UID:6409-1563363000-1563366600@resources.govsci.com
SUMMARY:Webinar: Single Cell Analysis with the MVX-7100 µL Workstation
DESCRIPTION:Join us for this webinar that will discuss single cell analysis with the MVX-7100 µL Workstation – low volume sample introduction. The webinar will cover the following topics: \n\nAn introduction to cell analysis with ICP-MS\nThe ‘Single Cell Analysis’\n\n\nWhat is this?\nWhy is this important?\nThe important analytical variables\n\n\nFrom sample to data: the single cell workflow\n\n\nAutomation\nThe glassware interface\nICP-MS\n\n\nWider analytical considerations\n\nPete Winship\, Teledyne CETAC MVX-7100 µL Workstation and SDX HPLD Product Manager will be presenting this webinar. \nThe presentation will last approximately 40 minutes and will include a question and answer session to follow.
URL:https://resources.govsci.com/event/webinar-single-cell-analysis-with-the-mvx-7100-%c2%b5l-workstation/
LOCATION:From your desktop or mobile device
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/png:https://resources.govsci.com/wp-content/uploads/2019/07/Single-Cell-Analysis-Webinar.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20190618T080000
DTEND;TZID=America/New_York:20190618T090000
DTSTAMP:20260611T070626
CREATED:20190607T175335Z
LAST-MODIFIED:20190919T160459Z
UID:5939-1560844800-1560848400@resources.govsci.com
SUMMARY:Webinar: An Introduction to characterization of biomolecules using analytical ultracentrifugation
DESCRIPTION:ABSTRACT:\n\n\nDATE: June 18\, 2019\nTIME: 8:00am PDT\n\nAnalytical Ultracentrifugation (AUC) is one of the most powerful biophysical tools used today for the characterization of biological samples ranging from small drug molecules to intact viruses\, vesicles and microparticles. AUC works with biological samples in the native state and does not depend on a reporter species or custom-coated substrates which are required by techniques such as NMR\, EPR\, SPR and fluorescence spectroscopy. AUC separates biomolecules based upon both molecular mass and anisotropy\, unlike Size Exclusion Chromatography (SEC)\, which separates molecules based only on their hydrodynamic volume. Furthermore\, AUC is not just useful for characterizing the oligomerization/aggregation state of biological samples\, but also to quantify interactions between different species.\nIn this talk\, we will start with the principles of analytical ultracentrifugation and take a tour through the technology behind modern AUC\, including UV/Vis absorbance mode and interference mode signal detection\, and look at experiment design and setup. Following\, we will address the different types of AUC experiments (equilibrium and velocity)\, compare and contrast their merits with sample data\, and touch upon the principles of data processing (to be covered in-depth in a subsequent webinar). Finally\, we will explore a variety of applications with a focus on the unique advantages that AUC brings to the study of various biotherapeutics\, polymers\, nanoparticles\, and others – and how AUC compares to and complements other analytical techniques.\nLearning Objectives:\n\n\nBecome familiar with the principles of analytical ultracentrifugation\, the technology behind modern AUC.\n\n\nLearn the fundamentals of how to design and setup experiments.\n\n\nLearn about the different types of AUC experiments (equilibrium and velocity)\, compare and contrast their merits.\n\n\nLearn the basic principles behind AUC data analysis.\n\n\nDiscover the unique advantages that AUC brings to the study of various biotherapeutics\, polymers\, nanoparticles\, etc.\n\n\n\nLabRoots is approved as a provider of continuing education programs in the clinical laboratory sciences by the ASCLS P.A.C.E. ® Program. By attending this webinar\, you can earn 1 Continuing Education credit once you have viewed the webinar in its entirety.\n\n\n\n\nAkash Bhattacharya\, PhD\n\nSenior Application Engineer\, Beckman Coulter Life Sciences\n\n\n\nAkash Bhattacharya graduated from Presidency College\, India with a major in Physics and went on to a Masters’ in Physics at the Indian Institute of Science where he worked on Quantum Computing. He then moved for doctoral studies in Biophysics to the University of Michigan\, Ann Arbor where he joined the lab of Prof. Erik Zuiderweg and worked on NMR spectroscopy methods development in the context of the Structural Biology of Chaperone Proteins. After Michigan\, he worked briefly at Rutgers and then eventually moved to the Dept. of Biochemistry and Structural Biology at the University of Texas Health at San Antonio. Here\, he worked with Prof. Dmitri Ivanov and Prof. Borries Demeler on the enzymology of HIV infection and restriction by mammalian proteins. He also worked on projects related to oncology (DNA damage repair) and neuroscience (voltage gated ion channels)\, using a wide variety of techniques ranging from X-ray crystallography\, NMR spectroscopy\, fluorescence spectroscopy\, molecular dynamics and analytical ultracentrifugation (AUC). He collaborated with Prof. Demeler to extend AUC methods to novel enzymatic systems resulting in publications in PNAS\, Cell Reports\, Nature Scientific Reports\, etc. Akash joined Beckman Coulter Life Sciences in Oct 2018. He is based in the Colorado R&D center and works on developing new AUC applications. His research interests include extending AUC methodology to new therapeutic areas such as AAV capsids (gene therapy)\, liposomal drug carriers and others.\n\n\n\nRoss VerHeul\n\nSenior Applications Scientist – Beckman Coulter\n\n\n\nRoss holds formal training spanning biology to synthetic organic chemistry and wide-ranging expertise in microfluidic applications paired with the production\, purification\, and characterization of a multitude of biomaterials for use in vitro and in vivo. Such materials include synthetic and natural proteins\, polymers\, nanoparticles\, and viral & non-viral vectors for gene therapy.\n\nWatch on Demand
URL:https://resources.govsci.com/event/an-introduction-to-characterization-of-biomolecules-using-analytical-ultracentrifugation/
LOCATION:From your desktop or mobile device
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/png:https://resources.govsci.com/wp-content/uploads/2019/06/BeckmanLogoNoLifeSci_HiRez.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20190613T120000
DTEND;TZID=America/New_York:20190613T120000
DTSTAMP:20260611T070626
CREATED:20190614T181704Z
LAST-MODIFIED:20190614T182558Z
UID:6137-1560427200-1560427200@resources.govsci.com
SUMMARY:Neuroimmune Interactions in Development\, Health\, and Disease
DESCRIPTION:Overview:\nIt is increasingly appreciated that crosstalk at the nexus of the nervous and immune systems mediates a delicate balance between dysregulation and homeostasis across many important biological processes. In this Cell Press webinar\, three speakers will explore emerging developments in our understanding of mediators and mechanisms of neuro-immune interplay. \nOur three speakers come from labs which are researching:\n\nHow the immune system deals with T. gondii\nAn understanding of how dysfunctional neuron-glia interactions contribute to neuropsychiatric diseases\nHow neuron-glia communication facilitates the formation\, elimination and plasticity of synapses during both healthy development and disease\n\nDuring the webinar\, viewers will:\n\nHear of interactions between neurons\, glial cells and immune signals\nGlimpse into potential future advances\nHave the opportunity to ask questions during the live broadcast.\n\nSpeakers:\nDr. Christopher Hunter\nUniversity of Pennsylvania \n \n  \n  \n  \nDr. Anna Molofsky\nUniversity of California\, San Francisco \n \n  \n  \n  \nDr. Beth Stevens \nHarvard Medical School \n \n  \n  \n  \n  \nWatch On Demand
URL:https://resources.govsci.com/event/neuroimmune-interactions-in-development-health-and-disease/
CATEGORIES:Webinar
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20190613T000000
DTEND;TZID=America/New_York:20190613T000000
DTSTAMP:20260611T070626
CREATED:20190613T133150Z
LAST-MODIFIED:20190617T143236Z
UID:6051-1560384000-1560384000@resources.govsci.com
SUMMARY:An Introduction To Cell Culture
DESCRIPTION:This webinar will introduce the history\, theory\, basic techniques\, and potential pit-falls of mammalian cell culture. It is designed for students and new lab technicians\, as well as bench scientists interested in updating their techniques or knowledge in the field. \nTopics to be discussed include:\n• History and practical theories of cell culture and its impact on today’s science\n• The requirements needed to set up a cell culture laboratory\n• Challenges when performing mammalian cell culture and how to overcome them \nAbout our Presenter:\nDr. Mark Rothenberg graduated from Emory University with his Ph.D. in Cell and Developmental Biology. Over the past 25 years\, Mark has held positions in both academia and industry where he has developed an expertise in the areas of assay development and cell culture. He currently holds the position of Manager Scientific Training and Education with Corning Life Sciences. \nWatch On Demand
URL:https://resources.govsci.com/event/an-introduction-to-cell-culture/
CATEGORIES:Webinar
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20190521T110000
DTEND;TZID=America/New_York:20190521T120000
DTSTAMP:20260611T070626
CREATED:20190521T174608Z
LAST-MODIFIED:20190716T185640Z
UID:5806-1558436400-1558440000@resources.govsci.com
SUMMARY:Overcoming Common Challenges in Waste & Surface Waters Analysis
DESCRIPTION:Event Overview: \nLaboratories performing wastewater\, surface water\, and effluent testing contend with a multitude of demands: \n\nAnalyzing a diverse range of contaminants\, which mandates a variety of methods and techniques while managing a large volume of samples\nBalancing high throughputs\, low instrument downtime with high sensitivity and reliable results\n\nA “one size fits all” approach may not be the best solution for your laboratory.  The correct analytical technique coupled with the proper sample preparation technique can streamline your wastewater analyses and ultimately improve your profitability\, operating margins and efficiency.  Examining these new advances and how they can bring significant return on investment (ROI) for modernizing your laboratory will be discussed. \nKey Learning Objectives: \n\nLearn about new technological advances in mature techniques for inorganic constituents in surface and waste waters\nGain insights on best practices to reduce reruns and improve sample throughput\nDiscover invaluable approaches to deal with the challenges of interferences from complex wastewater matrices\nAddress how to analyze both high and low concentration elements simultaneously\nExpand understanding of stay-clean technology in the newest GC–MS approaches\nLearn specific injector techniques for organic contaminants that enhance sample recovery and reporting limits\nFind out about new organic detectors that extend dynamic range and how to optimize them for use with alternative carrier gases\n\nWho Should Attend: \n\nLaboratory technicians who perform waste and surface water analyses for their clients\nWater quality scientists or chemists working with public water supplies or water treatment facilities\nAcademia research scientists\, chemists or laboratory department managers analyzing waste or surface water quality trends\nLaboratory managers and directors who are tasked with improving productivity and profit margins for the lab operations they oversee\n\n \n  \nRuth Wolf\nPrincipal Field Application Scientist\, Atomic/Mass Spectroscopy\nPerkinElmer\, Inc. \n  \nRuth has 20 years’ experience working as an analytical chemist in a variety of fields including environmental and geochemical analysis\, analytical methods development\, instrumentation development\, and technical sales and marketing. She returned to PerkinElmer\, Inc.\, as a Senior Field Application Scientist in 2016 after spending 12 years at the U.S. Geological Survey (USGS) as a Research Chemist. She has a Ph.D. in Chemistry from Colorado State University and an M.B.A. from the University of Connecticut. \n \n  \nLee Marotta\nPrincipal Field Application Scientist\, Gas Chromatography\nPerkinElmer\, Inc. \n  \nLee Marotta is a Principal Field Application Scientist with PerkinElmer. She started her career at Exxon Corporate Research as a chromatographer. Since Exxon\, Lee has over 25 years’ experience as a field application scientist with PerkinElmer. She focuses on the petroleum and environmental industries\, engaging with customers to understanding their challenges and requirements to ultimately help them realize success. She has a B.S. in Chemistry and Biology from Rutgers University. \nWATCH ON DEMAND
URL:https://resources.govsci.com/event/overcoming-common-challenges-in-waste-surface-waters-analysis/
CATEGORIES:Webinar
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20190418T110000
DTEND;TZID=America/New_York:20190418T120000
DTSTAMP:20260611T070626
CREATED:20190313T143020Z
LAST-MODIFIED:20190313T143020Z
UID:4758-1555585200-1555588800@resources.govsci.com
SUMMARY:Solutions for Light Hydrocarbons and Gases:  PLOT Columns
DESCRIPTION:Date and time:\nThursday\, April 18\, 2019 11:00 am\nEastern Daylight Time (New York\, GMT-04:00)\n\n\n\nThursday\, April 18\, 2019 8:00 am\nPacific Daylight Time (San Francisco\, GMT-07:00)\n\n\n\nThursday\, April 18\, 2019 5:00 pm\nEurope Summer Time (Berlin\, GMT+02:00)\n\n\nProgram:\n\n2018-2019 Agilent GC and GC/MS Chemistries and Supplies Webinar Series\n\n\n\nPanelist(s) Info:\n\nAllen K. Vickers\, Product Development Chemist\, Agilent Technologies Inc.\n\n\n\nDuration:\n1 hour\n\n\nDescription:\n\n\n\n\n\n\nPLOT (Porous Layer Open Tubular) columns are intended for the separation of compounds with very high vapor pressure (e.g.\, permanent gases and light hydrocarbons) without the need for cryogenic or sub-ambient cooling of the oven. PLOT column stationary phases are physically different than those of polysiloxanes and polyethylene glycols. PLOT stationary phases are porous particles that are attached to the inner wall of the capillary tubing using a binder or similar means. Compounds are separated based on their adsorption properties and other gas-solid surface interactions with the stationary phase.Agilent offers the most comprehensive line of PLOT columns for analysis of fixed gases\, low molecular weight hydrocarbon isomers\, volatile polar compounds\, and reactive analytes such as sulfur gases\, amines\, and hydrides. In this presentation we will cover the modes of separation involved with PLOT columns and demonstrate a wide array of separations including permanent gases\, branched and olefinic hydrocarbons\, and sulfur compounds among others. \nPresenter Information: Allen K. Vickers\, Product Development Chemist\, Agilent Technologies Inc. \n\n\n\n\n \nPlease visit this link and register today at: Agilent Webinar GC Columns
URL:https://resources.govsci.com/event/solutions-for-light-hydrocarbons-and-gases-plot-columns/
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/jpeg:https://resources.govsci.com/wp-content/uploads/2019/03/WebinarGC.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20190319T110000
DTEND;TZID=America/New_York:20190319T120000
DTSTAMP:20260611T070626
CREATED:20190313T140914Z
LAST-MODIFIED:20190313T140914Z
UID:4749-1552993200-1552996800@resources.govsci.com
SUMMARY:Making a Grand Entrance:  Techniques for Efficient Sample Introduction\, Inlet Types\, and Maintenance
DESCRIPTION:Date and time:\nTuesday\, March 19\, 2019 11:00 am\nEastern Daylight Time (New York\, GMT-04:00)\n\n\n\nTuesday\, March 19\, 2019 8:00 am\nPacific Daylight Time (San Francisco\, GMT-07:00)\n\n\n\nTuesday\, March 19\, 2019 4:00 pm\nEurope Time (Berlin\, GMT+01:00)\n\n\nProgram:\n\n2018-2019 Agilent GC and GC/MS Chemistries and Supplies Webinar Series\n\n\n\nPanelist(s) Info:\n\nMark Sinnott\, Application Engineer\, Agilent Technologies\, Inc.;Alex Ucci\, Application Engineer\, Agilent Technologies\, Inc.\n\n\n\nDuration:\n1 hour\n\n\nDescription:\n\n\n\n\n\n\nSample introduction is arguably one of the most important aspects in being successful at Gas Chromatography. The vast majority of problems that arise in GC are inlet or “front-end” related. If your sample is not introduced properly to the inlet and column\, all bets are off for producing a useful high-resolution chromatogram. In this presentation we will discuss the various types of GC inlets available including when and how to use them. We will also discuss proper inlet maintenance techniques to keep your application running strong. Presenter Information: \n Mark Sinnott\, Application Engineer\, Agilent Technologies\, Inc. \nMark Sinnott works for Agilent Technologies as a Technical Support Engineer in the Consumables and Supplies Division (CSD) at the capillary column manufacturing facility (the “J&W Scientific” location). In his position at Agilent\, Mark performs technical support and applications assistance to gas chromatographers worldwide. He has more than 22 years of experience in gas chromatography\, including environmental analysis of compounds in air\, soil and water matrices\, including dissolved gas analysis for the electrical industry. Mark holds a Master’s Degree in Chemistry from California State University\, Sacramento\, and currently resides in Sacramento. \nAlex Ucci\, Application Engineer\, Agilent Technologies\, Inc. \nIn his current position at Agilent\, Alex provides application assistance and technical support for sample preparation products as well as GC and LC consumables. Before he joined Agilent in 2014\, Alex was a graduate student at the Pennsylvania State University researching the morphology and surface properties of aerosol particles using a wide variety of analytical techniques. He has an MS degree in chemistry. \n \n\nPlease visit this link and register today at: Agilent Webinar GC Columns
URL:https://resources.govsci.com/event/making-a-grand-entrance-techniques-for-efficient-sample-introduction-inlet-types-and-maintenance/
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/jpeg:https://resources.govsci.com/wp-content/uploads/2019/03/WebinarGC.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20190228T133000
DTEND;TZID=America/New_York:20190228T143000
DTSTAMP:20260611T070626
CREATED:20190207T142516Z
LAST-MODIFIED:20190207T142516Z
UID:4019-1551360600-1551364200@resources.govsci.com
SUMMARY:Amino Acid Analysis:  Challenges and Solutions
DESCRIPTION:Amino acids are small molecules that serve as fundamental building blocks in a cell. They play a vital role in a variety of physiological mechanisms.\nQuantitation of amino acids to understand and monitor cell function has historically been a challenge to researchers.\nThis presentation will not only shed light on the challenges in amino acid analysis but also present ways of addressing those challenges.\n\n \n  \nSpeakers\n\n\n\n\nLaks Iyer\, Ph.D.\nPrincipal Product Manager\nWaters Corporation\n  \nLaks Iyer Ph.D. is a Principal Product Manager with Chemistry Technology Center at Waters Corporation.\nHis background is in biochemistry\, neuroscience and molecular biology. He has over 15 years of experience with life science research products.\n \n  \n\n\n \n\n\n\nPadhraic Rossiter\nProduct Development Chemist\nWaters Corporation\, Wexford\, Ireland\n \n \n\nPadhraic Rossiter is a Product Development Chemist at the Waters Reagent Kit Development Centre in Wexford\, Ireland. His background is Chemistry and Biochemistry.\nHe has been involved in the development and manufacture of reagent kits for over 7 years and has been working on the amino acid application for 2 years. \nREGISTER HERE
URL:https://resources.govsci.com/event/amino-acid-analysis-challenges-and-solutions/
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/png:https://resources.govsci.com/wp-content/uploads/2019/02/WatersWebinar2.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20190219T110000
DTEND;TZID=America/New_York:20190219T120000
DTSTAMP:20260611T070626
CREATED:20190212T210258Z
LAST-MODIFIED:20190212T210258Z
UID:4228-1550574000-1550577600@resources.govsci.com
SUMMARY:Redefining Automated RNA Isolation Using Advanced Sample Preparation Kits with a Digital Automated Platform
DESCRIPTION:How are your RNA yields? In some cases\, sample types present special challenges in RNA purification and analysis. In this webinar\, we will discuss and provide tips for the following topics: \n• The basic methods and challenges of RNA purification \n• Special considerations for challenging sample types \n• Solutions for automated RNA sample purification \nSpeaker: Inga Irle\, Ph.D.\, Senior Strategic Marketing Manager – QIAGEN  \nDr. Inga Irle obtained her Master of Science degree in Biochemistry in 2006 from the Ruhr University in Bochum\, Germany\, focusing on molecular medicine and biomarker discovery. She received her Ph.D. in 2009 at the University of Duisburg-Essen\, where she worked in the field of cancer and epigenetics. Dr. Irle joined QIAGEN in 2010 and was Global Product Manager for various products\, including qPCR and Epigenetics. She currently is a Senior Strategic Marketing Manager for QIAGEN’s automated solutions for Life Science. \nRegister Here
URL:https://resources.govsci.com/event/redefining-automated-rna-isolation-using-advanced-sample-preparation-kits-with-a-digital-automated-platform/
LOCATION:From your desktop or mobile device
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/png:https://resources.govsci.com/wp-content/uploads/2019/02/QIAGENWebinarRNAIsolation.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20190213T110000
DTEND;TZID=America/New_York:20190213T121500
DTSTAMP:20260611T070626
CREATED:20190208T183656Z
LAST-MODIFIED:20190208T183656Z
UID:4078-1550055600-1550060100@resources.govsci.com
SUMMARY:switchSENSE® - Biophysical Analysis with Electro-Switchable Biosurfaces
DESCRIPTION:Please join us to learn more about dynamicBIOSENSORS’ pioneering switchSENSE® sensor platform: an automated\, fluorescence based biosensor chip technology that employs electrically actuated DNA nanolevers for biophysical and interaction analysis measurements! \nThe real-time measurement of binding kinetics of interactions between proteins\, DNA/RNA\, and small molecules can be detected with femto-molar sensitivity. The platform offers an automated ligand density control for the measurement of affinity and avidity binding modes in one single assay. Using minimal amounts of sample\, protein diameters and conformational changes are analyzed with 0.1 nm accuracy\, as well as protein melting transitions.  \nAs a world’s first\, our double color DRX² analyzer enables the simultaneous measurement of two different species of probes on the same detection spot. This offers the possibility of on-spot referencing or dual binding modelling\, which is ideal for bispecific and proof-of-action experiments. Our webinar will cover the different measurement modes of our novel switchSENSE® technology\, as well as its applications in biophysical analysis. \nREGISTER HERE
URL:https://resources.govsci.com/event/switchsense-biophysical-analysis-with-electro-switchable-biosurfaces/
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/jpeg:https://resources.govsci.com/wp-content/uploads/2019/02/DynabioBanner.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20190122T130000
DTEND;TZID=America/New_York:20190122T140000
DTSTAMP:20260611T070626
CREATED:20190107T214400Z
LAST-MODIFIED:20190107T214400Z
UID:3703-1548162000-1548165600@resources.govsci.com
SUMMARY:Enabling and Optimizing High Quality Spectral Flow Cytometry Analysis: The Cytek Aurora and FCS Express Synergistic Solution
DESCRIPTION:Cytek Biosciences and De Novo Software are proud to announce a collaboration to allow you to work with your spectral analysis data files directly in FCS Express. The partnership brings a powerful combination of cutting edge spectral flow cytometry technology together with data analysis tools designed to get you results in record time. In addition\, all new Aurora and Northern Lights cytometers will now include FCS Express. \nJoin us for an exciting and educational webinar to learn how to implement the complimentary technologies of Cytek and De Novo Software in your everyday analysis. Whether you are new to spectral flow cytometry or have been using the technology for years this webinar is for you. \nThe joint webinar will cover an introduction to spectral flow cytometry technology using Cytek’s intuitive systems with a focus on dye selection\, working with fluorochrome signatures\, and quality control to acquire highly multiparametric data sets with unparalleled ease. The team from De Novo Software will discuss how to integrate Spectral Plots in FCS Express to your everyday analysis to facilitate reporting\, quality control\, statistics\, batch analysis\, and publication ready figures. \nREGISTER HERE
URL:https://resources.govsci.com/event/enabling-and-optimizing-high-quality-spectral-flow-cytometry-analysis-the-cytek-aurora-and-fcs-express-synergistic-solution/
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/png:https://resources.govsci.com/wp-content/uploads/2019/01/Enabling-and-Optimizing-High-Quality-Spectral-Flow-Cytometry-Analysis-The-Cytek-Aurora-and-FCS-Express-Synergistic-Solution.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20190114T130000
DTEND;TZID=America/New_York:20190114T140000
DTSTAMP:20260611T070626
CREATED:20190104T134717Z
LAST-MODIFIED:20190104T134717Z
UID:3662-1547470800-1547474400@resources.govsci.com
SUMMARY:Introduction to the new CLC Genomics Workbench 12
DESCRIPTION:QIAGEN is proudly introducing a new bioinformatics analysis tool\, CLC Genomics Workbench 12\, designed to bring the robustness and sophistication of the company’s industry-leading sequencing analysis solutions to biologists without bioinformatics training. The new tool works with any biological variant\, in any species\, for any application. \nIn this webinar\, we will present a sneak preview of the basic features and showcase selected improvements in the new CLC Genomics Workbench 12. The following topics will be addressed: \n\nOverview of the Workbench user interface\nPlugins – Biomedical Genomics Analysis Module\nNew Reference Data Manager\nRunning individual tools or workflows\nBatch analysis of data\nData visualization with the new improved Genome Browser\n\nREGISTER HERE \nSpeaker:\nPrakriti Mudvari\, PhD\nSenior Scientist – QIAGEN
URL:https://resources.govsci.com/event/introduction-to-the-new-clc-genomics-workbench-12/
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/png:https://resources.govsci.com/wp-content/uploads/2019/01/Learn-what’s-new-in-the-new-CLC-Genomics-Workbench-12.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20181212T130000
DTEND;TZID=America/New_York:20181212T140000
DTSTAMP:20260611T070626
CREATED:20181108T142702Z
LAST-MODIFIED:20181108T142702Z
UID:3343-1544619600-1544623200@resources.govsci.com
SUMMARY:Waters: Processing and Interpreting LC/Time-of-Flight MS Data
DESCRIPTION:Mass spectrometry (MS) is becoming more and more common in the day-to-day work of analytical scientists either as a supplement to\, or enhancement of\, UV and other optical-based measurements. The additional information provided by mass spectrometry is of value in a variety of assays across multiple application areas. For example\, Time-of-Flight (TOF) mass spectrometry provides accurate mass measurement for compound confirmation or identification of unknown species. It can also provide enhanced specificity over traditional MSMS techniques in quantitative assays. \nIn this series of webinars\, we will review the concepts of Time-of-Flight (TOF) mass spectrometry. The first seminar of the series will focus on the basic principles of TOF-MS and a comparison with other mass spectrometric techniques. This will be followed by a discussion of the considerations for coupling ESI-MS to liquid chromatography\, including MS-compatible mobile phases. The final webinar will review how to process and interpret the resulting data for both traditional small molecule applications and biopharmaceutical applications. Throughout the webinar series\, practical examples and tips will be shared so that new users of the technique will gain insights that can be put to immediate use. \nREGISTER HERE \nPresenter\nMichael Daly\nSenior Principal Field Applications Specialist\nWaters Corporation
URL:https://resources.govsci.com/event/waters-processing-and-interpreting-lc-time-of-flight-ms-data/
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/jpeg:https://resources.govsci.com/wp-content/uploads/2018/11/meet_the_experts_banner_template_webinar_on24_990px.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20181205T130000
DTEND;TZID=America/New_York:20181205T140000
DTSTAMP:20260611T070626
CREATED:20181108T141937Z
LAST-MODIFIED:20181108T142737Z
UID:3340-1544014800-1544018400@resources.govsci.com
SUMMARY:Waters: Practical Tips for Coupling Time-of-Flight MS with Liquid Chromatography
DESCRIPTION:Mass spectrometry (MS) is becoming more and more common in the day-to-day work of analytical scientists either as a supplement to\, or enhancement of\, UV and other optical-based measurements. The additional information provided by mass spectrometry is of value in a variety of assays across multiple application areas. For example\, Time-of-Flight (TOF) mass spectrometry provides accurate mass measurement for compound confirmation or identification of unknown species. It can also provide enhanced specificity over traditional MSMS techniques in quantitative assays. \nIn this series of webinars\, we will review the concepts of Time-of-Flight (TOF) mass spectrometry. The first seminar of the series will focus on the basic principles of TOF-MS and a comparison with other mass spectrometric techniques. This will be followed by a discussion of the considerations for coupling ESI-MS to liquid chromatography\, including MS-compatible mobile phases. The final webinar will review how to process and interpret the resulting data for both traditional small molecule applications and biopharmaceutical applications. Throughout the webinar series\, practical examples and tips will be shared so that new users of the technique will gain insights that can be put to immediate use. \nREGISTER HERE \nPresenter\nPaula Hong\, Ph.D.\nPrincipal Scientist\nWaters Corporation
URL:https://resources.govsci.com/event/waters-practical-tips-for-coupling-time-of-flight-ms-with-liquid-chromatography/
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/jpeg:https://resources.govsci.com/wp-content/uploads/2018/11/meet_the_experts_banner_template_webinar_on24_990px.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20181204T110000
DTEND;TZID=America/New_York:20181204T120000
DTSTAMP:20260611T070626
CREATED:20181207T200833Z
LAST-MODIFIED:20181207T200833Z
UID:3540-1543921200-1543924800@resources.govsci.com
SUMMARY:MILLIPORESIGMA: INNOVATIONS IN FOOD ANALYSIS USING SPME-DART®/MS
DESCRIPTION:Lab Manager is hosting a joint webinar from MilliporeSigma® and IonSense featuring an innovative workflow for food analysis applications. The SPME-DART®/MS workflow offers isolation of analytes by either direct immersion into food and beverages or extraction from headspace. This is followed by direct analysis without further sample processing or the need for GC or LC separation. Learn more about the many advantages of SPME-DART®/MS by registering for this exciting webinar! \nWATCH ON DEMAND \nKey Learning Objectives \n\nHow SPME-DART®/MS methods can increase lab efficiency\nAdvantages of SPME compared to traditional sample prep techniques\nBenefits of DART/MS over LC/MS or GC/MS\n\nWho Should Attend?\nAnyone interested in innovations in food and beverage analysis\, including: \n\nAnalytical Chemists\nMethod Developers\nLaboratory Manager\, Directors\, Supervisors\n\nSpeaker\nBrittany Laramee\nProduct Specialist\nIonSense\, Inc.
URL:https://resources.govsci.com/event/milliporesigma-innovations-in-food-analysis/
CATEGORIES:Webinar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20181129T110000
DTEND;TZID=America/New_York:20181129T120000
DTSTAMP:20260611T070626
CREATED:20181106T165812Z
LAST-MODIFIED:20181213T133204Z
UID:3289-1543489200-1543492800@resources.govsci.com
SUMMARY:IncuCyte: Longitudinal Characterization of Human Stem Cell-Derived Neurons Using Calcium Imaging
DESCRIPTION:Webinar abstract \nThe ability to measure neuronal activity and network activity in a longitudinal manner is paramount to the study of neurological disease Due to the synaptic plasticity of neuronal cell cultures\, identifying dynamic changes between normal and mutated models is critical for understanding changes in network connectivity. To evaluate activity differences between normal and diseased states\, we used mutant and control human induced pluripotent stem cells (iPSCs) to generate neuronal cultures by forcing expression of Neurogenin-2. Using the IncuCyte® S3 live-cell analysis system\, we measured neuronal activity over the course of several weeks for functional analysis of differences in activity and connectivity. We found that iPSC-derived neurons had increased activity over time and formed synchronous neuronal networks around 3 weeks of differentiation. Data generated showed a reproducible\, relevant phenotypic readout for long-term network changes in this epileptic cell model. \nWATCH ON DEMAND \nLearn how to: \n\nDifferentiate iPSCs into neurons using forced Neurogenin-2 expression\nAcquire and analyze calcium imaging data over time\, using the IncuCyte® S3 live-cell analysis system\nThe importance of long-term analysis of neuronal activity to evaluate differences in activity and connectivity for iPSC derived neurons\n\nPresenter: Louis Dang\, MD/PhD\, Clinical Lecturer\, University of Michigan \nLouis Dang is a pediatric epileptologist and neuroscientist at the University of Michigan. His research focuses on how genetic mutations cause early-life epilepsies. Using patient-derived and gene-edited stem cells\, he generates 2D and 3D cultures to determine the molecular pathogenesis of epilepsy\, opening new avenues for targeted therapies.
URL:https://resources.govsci.com/event/incucyte-longitudinal-characterization-of-human-stem-cell-derived-neurons-using-calcium-imaging/
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/png:https://resources.govsci.com/wp-content/uploads/2018/11/Longitudinal-Characterization-of-Human-Stem-Cell-Derived-Neurons-Using-Calcium-Imaging.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20181128T130000
DTEND;TZID=America/New_York:20181128T140000
DTSTAMP:20260611T070626
CREATED:20181108T141548Z
LAST-MODIFIED:20181108T142849Z
UID:3335-1543410000-1543413600@resources.govsci.com
SUMMARY:Waters: What Is Time-of-Flight Mass Spectrometry and How Is It Used?
DESCRIPTION:Mass spectrometry (MS) is becoming more and more common in the day-to-day work of analytical scientists either as a supplement to\, or enhancement of\, UV and other optical-based measurements. The additional information provided by mass spectrometry is of value in a variety of assays across multiple application areas. For example\, Time-of-Flight (TOF) mass spectrometry provides accurate mass measurement for compound confirmation or identification of unknown species. It can also provide enhanced specificity over traditional MSMS techniques in quantitative assays.  \nIn this series of webinars\, we will review the concepts of Time-of-Flight (TOF) mass spectrometry. The first seminar of the series will focus on the basic principles of TOF-MS and a comparison with other mass spectrometric techniques. This will be followed by a discussion of the considerations for coupling ESI-MS to liquid chromatography\, including MS-compatible mobile phases. The final webinar will review how to process and interpret the resulting data for both traditional small molecule applications and biopharmaceutical applications. Throughout the webinar series\, practical examples and tips will be shared so that new users of the technique will gain insights that can be put to immediate use. \nREGISTER HERE \nPresenter\nKieron Faherty\, Ph.D.\nSeparations & MS Field Marketing Manager\nWaters Corporation
URL:https://resources.govsci.com/event/waters-fundamentals-of-time-of-flight-tof-mass-spectrometry-part-1/
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/jpeg:https://resources.govsci.com/wp-content/uploads/2018/11/meet_the_experts_banner_template_webinar_on24_990px.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20181031T090000
DTEND;TZID=America/New_York:20181031T100000
DTSTAMP:20260611T070626
CREATED:20181029T201105Z
LAST-MODIFIED:20181211T195338Z
UID:3246-1540976400-1540980000@resources.govsci.com
SUMMARY:Improving RNA research results with LNA technology
DESCRIPTION:How does locked nucleic acid (LNA) technology affect RNA results? \nLNA (locked nucleic acid) oligos bind with much higher affinity and specificity to RNA targets than standard DNA and RNA oligos. This enables specific and sensitive detection of small RNAs and discrimination between highly similar sequences. This webinar will present the unique features and benefits of LNA and discuss how your microRNA qPCR experiments and your functional analyses of RNA will profit. \nLNA substitutions increase oligo melting temperature\, enabling Tm adjustment and normalization. This makes LNA optimal for designing short\, high-affinity PCR primers and antisense oligonucleotides. LNA also allows detection of rare RNAs\, even when limited to less sample material or complex samples with low RNA content. As LNA also increases the Tm difference between perfectly matched and mismatched targets\, even closely related sequences can be accurately discriminated in qPCR profiling and silencing. \nDue to their short length\, high-affinity LNA antisense oligonucleotides are taken up naturally by cells. Highly potent once inside cells and resistant to enzymatic degradation\, LNA antisense oligos effectively silence RNA in a broad range of animal tissues – making them the tool of choice for revealing RNA functions and evaluating their therapeutic potential. \nQIAGEN has merged our cutting edge technologies with Exiqon’s twenty years of experience in LNA oligo design to enhance qPCR technology\, in situ hybridization\, functional analysis of RNA in cells and animals\, miRNA and RNA sequencing and much more! Join this webinar and learn how to take your RNA research to the next level! \nREGISTER HERE \n• Live Webinar: Take your RNA research to the next level with LNA technology\n• Speaker: Roman Kurek\, Ph.D.\, Senior Customer Solutions Manager\, Genomics\, QIAGEN\n• Date and Time: October 31\, 2018 at 9:00 am EDT and 2:00 pm CET
URL:https://resources.govsci.com/event/improving-rna-research-results-with-lna-technology/
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/jpeg:https://resources.govsci.com/wp-content/uploads/2018/10/Take-your-RNA-research-to-the-next-level-with-LNA-technologies.jpeg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20181023T100000
DTEND;TZID=America/New_York:20181023T110000
DTSTAMP:20260611T070626
CREATED:20180906T192102Z
LAST-MODIFIED:20181025T174704Z
UID:2646-1540288800-1540292400@resources.govsci.com
SUMMARY:Promega: A Multi-Modal Assay for Quantitating and Interpreting Changes in Autophagic Flux
DESCRIPTION:This webinar is in collaboration with Aurelia Bioscience\, Nottingham\, UK. \nMonitoring autophagy using imaging or western blotting methods can be cumbersome\, low-throughput and subjective. Learn about a new LC3 reporter assay with three modalities (plate-reader based\, imaging and blotting) to help scale up your autophagy analysis with confidence. \nJoin us live to share your challenges with autophagy assays and test your knowledge of the pathway. \nWATCH ON DEMAND \nADDITIONAL WEBINAR INFORMATION: \nAre you studying autophagy or just getting started and want a simple\, add-mix-measure assay? Are you struggling to distinguish autophagy stimulation from late-phase pathway inhibition? Are you screening a large number of compounds and need a quantitative\, scalable assay? \nWhile imaging and western blotting are useful approaches for studying autophagy\, they can be challenging to interpret and have limited quantitative power. The new Autophagy LC3 HiBiT Reporter Assay enables you to unambiguously discern autophagy inducers from inhibitors with a quantitative\, plate-reader based readout. Implementing NanoBiT® and HaloTag®-based technology\, our autophagy reporter also allows for imaging and HiBiT blotting modalities to confirm mechanism of action as autophagy modulation\, and to discern early- versus late-phase pathway inhibition. \nJoin this live webinar to learn how the Autophagy LC3 HiBiT Reporter Assay can simplify your autophagy research. You’ll also hear about how Dr. Gary Allenby\, CSO and founder of Aurelia Biosciences\, benchmarked this autophagy assay against other assays for performance in high-throughput screening formats. \nPRESENTERS: DAN LAZAR\, PhD AND GARY ALLENBY\, PhD \nDr. Dan Lazar received his Ph.D. in biological chemistry from the University of Michigan and then completed a postdoctoral fellowship focused on cell signaling at Warner Lambert/Parke-Davis.  Subsequently\, he was a Team Leader and Senior Scientist at Eli Lilly within the metabolic disease drug-discovery area for well over a decade where he gained extensive experience in the development\, validation and implementation of cell-based and biochemical assays for drug discovery.  As a Group Leader and Senior Research Scientist at Promega\, Dan and his colleagues are principally focused on delivering novel cell-based assays for the quantitative assessment of various aspects of cell health to assist academic and industrial investigators. \nDr. Gary Allenby has a Ph.D. in reproductive toxicology\, and studied the pharmacology of retinoid biology as a post-doc at Hoffmann La Roche\, USA. He returned to the UK in 1995 to join the Lead Generation group at Glaxo Wellcome. There he developed cell-based assays for high throughput screening and worked with vendors to validate new technologies for screening and automated HTS. In 2000\, he joined the Hit Identification group at AstraZeneca\, developing assays for respiratory and inflammatory disease while continuing to work with vendors and automated assays. \nIn 2011\, Dr. Allenby became a founding entrepreneur of Aurelia Bioscience\, a pre-clinical contract research organization located in Nottingham\, UK. Aurelia Bioscience focuses on developing and implementing innovative cell-based assays for screening\, and collaborate with vendors to deliver value-adding data for drug discovery purposes.
URL:https://resources.govsci.com/event/promega-a-multi-modal-assay-for-quantitating-and-interpreting-changes-in-autophagic-flux/
CATEGORIES:Webinar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20181016T110000
DTEND;TZID=America/New_York:20181016T120000
DTSTAMP:20260611T070626
CREATED:20180904T161256Z
LAST-MODIFIED:20181213T133243Z
UID:2611-1539687600-1539691200@resources.govsci.com
SUMMARY:Agilent: Strategies to Avoid the Hidden Dangers of Suboptimal Sample Preparation and Simplify Your Workflow Simultaneously
DESCRIPTION:Summary \nA typical laboratory workflow comprises of sample collection\, sample preparation\, introduction to the instrument\, analysis\, data review\, and finally\, data reporting\, where sample preparation has always been considered the bottleneck and rate-limiting step. Current advanced instrumentation greatly increase your capability to analyze various samples\, considering the required sensitivity\, selectivity\, reliability\, and feasibility of complex sample testing. Therefore\, the sample preparation step has been minimized to reduce time\, cost\, and complexity\, improve the universal applicability\, and it has been reduced to be just good enough. \nThere are several hidden dangers in sub-optimal sample preparation\, such as wasted time\, instrument maintenance/failure issues\, and inaccurate data\, that can arise and affect your overall success. These hidden dangers can be eliminated or greatly minimized by proper sample preparation workflow strategies. This improvement can be realized without having to retrain your scientist\, making large capital expenditures\, or having to rewrite your standard operating procedures (SOPs).  The following Webinar will discuss how various samples with high lipid content are prepared with a simplified sample prep workflow utilizing Captiva EMR-Lipid. \nWATCH ON DEMAND \nView Whitepaper \n\n\n\n\n\n\n\nParticipants will learn: \n\nHow to minimize the hidden dangers of sub-optimal sample preparation\nA simplified workflow for complex samples with high lipid content\nAn understanding of the key applications where Captiva EMR—Lipid can maximize results and boost productivity\n\nWho Should Attend: \n\nLab Managers of contract\, government\, or QA/QC labs\nAnalytical chemists who develop methods for biological or food samples\nGraduate students and post-docs working on environmental\, pharmaceutical\, forensic\, or food analyses\n\nSpeakers \nGolnar Javadi\nTechnical Support Applications Engineer\nAgilent Technologies \n  \nAlex Ucci\nTechnical Support Applications Engineer\nAgilent
URL:https://resources.govsci.com/event/agilent-strategies-to-avoid-the-hidden-dangers-of-suboptimal-sample-preparation-and-simplify-your-workflow-simultaneously/
CATEGORIES:Webinar
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20181011T120000
DTEND;TZID=America/New_York:20181011T130000
DTSTAMP:20260611T070626
CREATED:20181004T151430Z
LAST-MODIFIED:20181004T151430Z
UID:3031-1539259200-1539262800@resources.govsci.com
SUMMARY:QIAGEN: What's the 'Plus' in QuantiFERON-TB Gold Plus?
DESCRIPTION:Join Dr. Masae Kawamura for an updated review of QuantiFERON-TB Gold Plus \nQuantiFERON-TB Gold Plus is approaching the first anniversary of its release to the US market. This milestone year has also been marked by a broad shift in global guidance towards TB blood testing for populations at increased risk for TB. The QFT-Plus test features innovative CD8 T cell technology that provides clinicians with a more comprehensive picture of a patient’s immune response to TB. Recent publications continue to demonstrate the benefits of QFT-Plus technology for at-risk patient populations – including studies of test efficacy for contact investigation\, healthcare worker screening and immunocompromised patients.  \nJoin Dr. Masae Kawamura for a dynamic discussion of the latest scientific advancements in TB testing and CD8 technology\, including a review of recent publications and a discussion of case scenarios applying the insights of QFT-Plus.  \nDisclaimer: QuantiFERON-TB Gold Plus (QFT-Plus) is an in vitro diagnostic aid for detection of Mycobacterium tuberculosis infection. QFT-Plus is an indirect test for M. tuberculosis infection (including disease) and is intended for use in conjunction with risk assessment\, radiography\, and other medical and diagnostic evaluations. QFT-Plus Package Inserts as well as up-to-date licensing information and product-specific disclaimers can be found at www.QuantiFERON.com. The performance of the USA format of the QFT-Plus test has not been extensively evaluated with specimens from individuals who have impaired or altered immune functions\, such as those who have HIV infection or AIDS or those who have transplantation managed with immunosuppressive treatment or others who receive immunosuppressive drugs (e.g.\, corticosteroids\, methotrexate\, azathioprine\, cancer chemotherapy) \nCan’t make it? Don’t worry! Register and you’ll receive a link to the webinar recording! \nREGISTER HERE \nPresenter:\nMasae Kawamura\, M.D. Senior Director\, Medical & Scientific Affairs – TB Diagnostics\, QIAGEN
URL:https://resources.govsci.com/event/qiagen-whats-the-plus-in-quantiferon-tb-gold-plus/
CATEGORIES:Webinar
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20181011T110000
DTEND;TZID=America/New_York:20181011T120000
DTSTAMP:20260611T070626
CREATED:20180911T141338Z
LAST-MODIFIED:20180911T141338Z
UID:2705-1539255600-1539259200@resources.govsci.com
SUMMARY:Agilent: Surviving Chromatography Part II Corrective Action
DESCRIPTION:Now you’re lost because your chromatography is not where it should be. What do you do? In this talk we’ll look at ways to troubleshoot what went wrong and discuss things you can do to keep them from happening in the future. \nIn this talk we’ll discuss: \n  \n\nCommon chromatography problems including pressure\, peak shape issues like tailing\, and retention time shifts\nHow to isolate the problem and whether it’s related to chemistry or your instrument hardware/software\nIdentifying the problem and taking corrective action can help prevent the same thing from happening in the future.\n\nREGISTER HERE \n  \nPresenter Information: Jean Lane\, Application Engineer\, Agilent Technologies\, Inc. \nJean has been employed with Agilent since Nov 2010 in technical and applications support and has a primary role supporting Agilent’s full line of LC columns and consumables\, which also includes support for Agilent’s GPC/SEC product line. She came to Agilent thru acquisition of Varian and the former Polymer Laboratories. \nJean has 20 plus years of technical and applications support for both HPLC and GPC consumable products. In addition to practical chromatography experience in the laboratory\, she has had many\, many years in her technical role involving customer support providing assistance and troubleshooting for customer chromatography issues. \n 
URL:https://resources.govsci.com/event/agilent-surviving-chromatography-part-ii-corrective-action/
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/jpeg:https://resources.govsci.com/wp-content/uploads/2018/09/Surviving-Chromatography-Part-II-Corrective-Action.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20181011T110000
DTEND;TZID=America/New_York:20181011T120000
DTSTAMP:20260611T070626
CREATED:20180904T144443Z
LAST-MODIFIED:20190104T150120Z
UID:2605-1539255600-1539259200@resources.govsci.com
SUMMARY:PerkinElmer: Tissue Biomarker Analysis: A Practical Approach for Translational Research
DESCRIPTION:Simultaneous quantitation of 6 or more biomarkers in intact tissue specimens holds the key to many questions concerning the biological basis of health and disease by allowing complex cellular interactions to be captured and analyzed. However\, reliable detection remains elusive due to technical challenges from many sources\, including antibody cross reactivity\, difficulty in balancing signals from rare and abundant targets\, tissue autofluorescence and interference between fluorophores\, especially for co-localized targets. \nIn this webinar application scientists from PerkinElmer will present a practical and validated method for highly multiplexed tissue biomarker analysis that addresses many of these challenges. Opal™ staining is an antibody-agnostic technique\, which produces highly specific and reproducible results and when combined with multispectral imaging systems\, such as Vectra®\, is able to detect eight or more biomarkers simultaneously in one tissue section. Simultaneous detection of multiple antigens on a single tissue with multispectral imaging and analysis reveals spatial relationships between cells with the resolution needed for high-precision proximity analysis and detection of intracellular localization of targeted antigens. By elucidating the relationships between cells\, Opal staining allows you to see intercellular relationships in context of the microenvironment. \nWATCH ON DEMAND \n\n\n\n\n\n\n\n\n\nIn this webinar\, you will learn: \n\nHow to overcome key challenges inherent in multiplex biomarker analysis\nPractical and validated approaches to multiplex IHC staining\nWhy multispectral imaging is important for generating high quality data\nMethods for analyzing relationships between cells\n\n  \n \nGrady Carlson\, PhD\nField Applications Scientist\,\nQuantitative Pathology Solutions\nPerkinElmer \n  \nLinden Wyatt\, PhD\nField Applications Scientist\,\nQuantitative Pathology Solutions\nPerkinElmer
URL:https://resources.govsci.com/event/perkinelmer-tissue-biomarker-analysis-a-practical-approach-for-translational-research/
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/jpeg:https://resources.govsci.com/wp-content/uploads/2018/09/webinar_header_banner_image_d328f37b7d3968afc867cc5d25576344efeda25f_8579.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20181009T140000
DTEND;TZID=America/New_York:20181009T150000
DTSTAMP:20260611T070626
CREATED:20180906T135337Z
LAST-MODIFIED:20180906T135337Z
UID:2631-1539093600-1539097200@resources.govsci.com
SUMMARY:Agilent: Gain Insights into Compliance Trends and Better Prepare for FDA Audits
DESCRIPTION:EVENT OVERVIEW:\nFDA warning letters and 483 observations provide valuable information that can be used to show trends in FDA regulatory focus and changes in auditing practices. Data Integrity has dominated FDA pharmaceutical warning letters in recent years and has harmonized regulators all over the world through common training\, exchange of information\, and collaboration. Analysis of FDA warning letters\, 483 information\, and other regulatory noncompliance data provides a more complete picture of regulatory actions and trends in FDA auditing practices. Laboratories can leverage this insightful regulatory data to understand evolution of FDA thinking and be better prepared for their next FDA audit. \nJoin compliance expert Paul Smith as he reviews where to find valuable non-compliance data\, how to use the data to identify insights\, and trends in FDA auditing practices. \nKEY LEARNING OBJECTIVES: \n\nWhere to access valuable non-compliance data\nHow to best leverage the data to identify insights\nCurrent evolutionary trends in FDA auditing practices\n\nREGISTER HERE \nPRESENTER: \nPaul Smith\nGlobal Strategic\nCompliance Specialist\nAgilent Technologies \n  \nWHO SHOULD ATTEND: \n\nExecutive suite\nLab operations managers (facilities/metrology)\nTechnicians/scientists\nQA/QC managers\nMetrology managers\nQuality director\n\n  \nSponsored by Agilent CrossLab. Presented by LC / GC. \nFor questions contact Kristen Moore at kristen.moore@ubm.com
URL:https://resources.govsci.com/event/agilent-gain-insights-into-compliance-trends-and-better-prepare-for-fda-audits/
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/png:https://resources.govsci.com/wp-content/uploads/2018/09/Aiglent-Webinar-Gain-Insights-into-Compliance-Trends-and-Better-Prepare-for-FDA-Audits.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20181009T130000
DTEND;TZID=America/New_York:20181009T140000
DTSTAMP:20260611T070626
CREATED:20180906T191509Z
LAST-MODIFIED:20181213T133038Z
UID:2643-1539090000-1539093600@resources.govsci.com
SUMMARY:Promega: Bottoms Up: Improving Proteomic Sample Preparation with Recombinant Asp-N and Multi-Enzyme Workflows
DESCRIPTION:While trypsin is the workhorse for bottom-up proteomics\, it is not a magic bullet since tryptic digestion often leaves gaps in protein sequences. In this webinar Dr. Hosfield will describe the advantages of using a new recombinant Asp-N protease to fill in the gaps. He will also demonstrate how combining digests from multiple proteases can yield comprehensive sequence coverage of proteins from a single LC-MS/MS run. \nWATCH ON DEMAND \nADDITIONAL WEBINAR INFORMATION: \nBottom-up mass spectrometry workflows typically use trypsin to digest proteins into peptides suitable for LC-MS/MS analysis. While trypsin is an excellent protease\, alternative proteases are useful for numerous applications including increasing protein sequence coverage and identifying post-translational modifications. \nIn this webinar Dr. Hosfield describes the features of a new recombinant Asp-N protease (rAsp-N). rAsp-N displays both high cleavage efficiency and a strong preference for cleavage N-terminal to aspartic acid. He will explain how this enzyme can be effectively used to digest a variety of sample types\, including complex protein mixtures and therapeutic molecules such as monoclonal antibodies. \nIn addition\, he describes how a multi-enzyme approach can be successfully employed to achieve 100% sequence coverage of an IgG from a single injection. Combining peptides derived from digestion with orthogonal proteases prior to LC-MS/MS analysis could be a general strategy to ensure high sequence coverage while simultaneously reducing demand on instrument time. \nPRESENTER: CHRIS HOSFIELD\nChris Hosfield is a Senior Research Scientist in the Protein Analysis group at Promega. He has lead the development of tools for proteomics and antibody characterization\, including PNGase F\, IdeS\, IdeZ and recombinant Asp-N. \nChris has broad expertise working with proteolytic enzymes and preparing protein samples for analysis by mass spectrometry. Prior to joining Promega\, Chris held senior scientist positions at several biotechnology companies where he applied proteomic methods to the discovery and development of both small molecules and biotherapeutics. He received his PhD in biochemistry from Queen’s University.
URL:https://resources.govsci.com/event/bottoms-up-improving-proteomic-sample-preparation-with-recombinant-asp-n-and-multi-enzyme-workflows/
CATEGORIES:Webinar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20181004T110000
DTEND;TZID=America/New_York:20181004T120000
DTSTAMP:20260611T070626
CREATED:20181003T144843Z
LAST-MODIFIED:20181003T144843Z
UID:3020-1538650800-1538654400@resources.govsci.com
SUMMARY:Metrohm: Challenges and Solutions for Sugar Analysis in Human Food\, Animal Feed\, and Pet Food
DESCRIPTION:Carbohydrates are an important component of the diet for both humans and animals. Given the recent scientific\, federal and consumer interest in carbohydrates\, specifically in added sugars\, it is important to establish actual sugar profile and composition in human food and beverages\, animal feed\, and pet foods. Sugar profile determination in food matrices helps to understand a product’s consistency and reduces vulnerability to food fraud. Nutritional sugar determination requires proper sample preparation\, matrix elimination\, and optimized separation and detection methods to achieve both precision and accuracy in complex food matrices. \nJoin us for an informational webcast on sugar testing and learn about key drivers for animal and human sugar measurements. Jeff Horst from Agri-King Inc. will discuss recent acceptance of Association of American Feed Control Officials (AAFCO) methods for sugars in animal feed\, pet food\, and human food that establish the initial necessary steps towards an AOAC-approved method for these challenging matrices. Dr. Hari Narayanan from Metrohm USA will discuss the latest developments in sample preparation that support sugar analysis in various human food matrices. \n  \nREGISTER HERE \n  \nKey Learning Objectives: \n\nNew regulations related to sugar analysis in human food\, animal feeds\, and pet foods\nIon chromatography methods for selective and sensitive sugar profiling\nRegulatory drivers for sugar analysis\nNew inline sample preparation techniques to achieve reproducible results\n\n  \nWho Should Attend: \n\nAnalytical development\, QA/QC lab managers from food and beverage companies\, human food\, pet food and animal feed manufacturers\nCommercial testing labs performing food sample analysis\nThose who are interested in learning ion chromatography and sugar analysis applications\nThose who are already using ion chromatography and wants to learn new sample preparation techniques\nAny one from pharmaceutical\, biopharmaceutical interested in learning about carbohydrate and fructans analysis\n\n  \nHave questions? Contact Kristen Moore at\,  \n  \nSPEAKERS \n\nJeff Horst\nLaboratory Production Manager\nAgri-King Inc\n\n\nJeff Horst is the Laboratory Production Manager at Agri-King Inc.\, an International Livestock Nutrition company based in Fulton\, IL. He has spent 28 years at Agri-King Inc.\, the past 17 as Laboratory Production Manager. Jeff is currently a Lab Advisor to Association of American Feed Control Officials (AAFCO) and serving as co-chairman of the Carbohydrate Working Group. He also serves on the National Forage Testing Association (NFTA) Board and is a past president. \n\n\n\nDr. Hari Narayanan\nProduct Marketing Manager\nMetrohm USA Inc\n\n\nDr. Hari Narayanan is the Product Marketing Manager at Metrohm USA Inc. He has eighteen years of experience in analytical chemistry\, focusing on IR\, Raman\, NIR spectroscopy and titration\, ion chromatography\, voltammetry\, XRF and several other analytical techniques. He developed several novel IC applications for the pharmaceutical industry and provided recommendations to USP for IC method updates. He received his B.Sc and M.Sc. in Chemistry from the MK University and a Ph.D. in Analytical Chemistry from the University of Madras\, India.
URL:https://resources.govsci.com/event/metrohm-challenges-and-solutions-for-sugar-analysis-in-human-food-animal-feed-and-pet-food/
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/png:https://resources.govsci.com/wp-content/uploads/2018/10/Challenges-and-Solutions.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20181003T140000
DTEND;TZID=America/New_York:20181003T150000
DTSTAMP:20260611T070626
CREATED:20180926T123445Z
LAST-MODIFIED:20181211T195540Z
UID:2938-1538575200-1538578800@resources.govsci.com
SUMMARY:Optimize Your GC Lab with On-Site Hydrogen Generation
DESCRIPTION:As laboratories and technologies change\, it is important to examine how we supply the gases needed within the laboratory.  This webcast will examine the role of both Hydrogen Lab Servers and benchtop Hydrogen Generators in optimizing your GC laboratory by saving time\, money\, space\, downtime\, headaches\, and in rare cases injury.  In addition\, we will discuss how gas generators can avoid interruptions from lack of availability or delivery issues that can be associated with the use of bottled gases.  This webcast will focus on how on-site Hydrogen Generators provide a steady stream of gas to your GC’s.  We will review advantages of on-site hydrogen gas generation\, including: \n\nCost Savings with minimal changes in expenditure year-after-year\nImprove your GC lab’s efficiency by those handling clumsy gas cylinders (decrease in time wasted)\nMaximizing safety\nDecreased down time with a 24/7\, on-demand\, reliable supply of Hydrogen\nPeace of mind with consistent carrier-grade purity\nBack-up options\n\nWATCH ON DEMAND \nKey Learning Objectives \n\nLearn how hydrogen generators work\nWhich applications are best suited for Hydrogen Gas Generators?\nCommon challenges of gas cylinder delivery and how Hydrogen Generators are the premier technical solution\nEasy installation for both benchtop hydrogen solutions as well as Hydrogen Lab Servers for larger GC applications\n\nWho Should Attend \n\nPetrochemical laboratory directors\nLaboratory managers\nLead Chemists\nGas purchasing agents\nChromatography specialists\nLaboratory personnel for refineries\n\nAttendees of the Live 1 Hour Webinar will receive a Professional Development Seminar Certificate of Completion issued by Proton OnSite. \nSpeaker \nScott Accetta\nRegional Manager\nProton OnSite\n\nScott Accetta is a Regional Manager for Proton OnSite and has been specializing in on-site gas generation solutions for many years.  He has extensive consultative experience in helping GC labs with hydrogen gas generation recommendations that are more cost-effective\, efficient\, convenient\, and safer than traditional delivered gas methods.  His expertise covers a broad range of industries including quality control\, petrochemical\, environmental\, agricultural\, academia\, forensics\, and more.  Scott’s gas generation application knowledge ranges from GC to LCMS and various types of spectroscopy. \n  \nWebinar Sponsored by:
URL:https://resources.govsci.com/event/optimize-your-gc-lab-with-on-site-hydrogen-generation/
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/png:https://resources.govsci.com/wp-content/uploads/2018/09/Optimize-Your-GC-Lab-with-On-Site-Hydrogen-Generation.png
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BEGIN:VEVENT
DTSTART;TZID=America/New_York:20181003T030000
DTEND;TZID=America/New_York:20181003T160000
DTSTAMP:20260611T070626
CREATED:20180920T162336Z
LAST-MODIFIED:20181211T195448Z
UID:2891-1538535600-1538582400@resources.govsci.com
SUMMARY:Agilent: Elevate the Performance of your GC (and MS): Strategies to Improve Sensitivity and Reliability with Complex Matrix Samples
DESCRIPTION:In an ideal world\, samples would always be clean\, easy to inject and analyse and your GC and MS systems would maintain their sensitivity indefinitely. The reality is that most samples cannot be directly injected onto the GC and MS detection system\, and sample preparation is often needed to achieve the desired sensitivity. Sometimes simple fixes\, such as choosing the right liner\, switching to a high efficiency column\, or utilizing “jet clean” on the MS can make a big difference on the sensitivity of the analysis.  But often\, sample preparation is the critical step needed to get samples ready for GC or GC/MS(-MS) analysis. Appropriate sample preparation techniques not only make samples amenable for GC injection at concentrations suitable for detection\, but also remove and prevent unwanted matrix components from accumulating and deteriorating on the GC and GC/MS flow path. We will discuss useful strategies\, including choosing the right GC column and supplies\, as well as what level of sample preparation\, and maintenance is required for method reliability and analytical data quality\, using challenging representative applications such as PAHs in salmon oil and pesticides in fatty matrices. \nWATCH ON DEMAND \nWhat does it cover? \nGC high efficiency columns and liner selection\, and sample preparation methods/techniques to improve the sensitivity and reliability of your GC and GC/MS analysis. \nBy attending this webinar you will learn: \n\nsome of the strategies you can employ when working with complex matrix samples\nhow to reduce instrument down time due to needed maintenance such as source cleaning\nhow sample preparation can benefit your GC and GC/MS(-MS) analysis.\n\nWhy should you attend? \nTo gain better understanding of: \n\nstrategies that can be implemented when working with complex matrix samples and still maintain the sensitivity and reliability of your GC and GC/MS(-MS) system.\nhow gas quality\, thermal stability\, and column bleed can affect your chromatography.\nsample preparation techniques/methods and their importance to improve method sensitivity and reliability.\n\nPLUS – Participation Bonus: Register and attend the webinar to receive a special offer from Agilent Technologies. \nThis presentation is suitable for… \nLaboratory technicians\, researchers\, and scientists wishing to learn more about how to analyse heavy matrix samples and learn about sample preparation.
URL:https://resources.govsci.com/event/agilent-elevate-the-performance-of-your-gc-and-ms-strategies-to-improve-sensitivity-and-reliability-with-complex-matrix-samples/
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/png:https://resources.govsci.com/wp-content/uploads/2018/09/Agilent.png
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END:VCALENDAR