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GenScript Biotech Reports First Half 2021 Results

GenScript Biotech Reports First Half 2021 Results
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GenScript to Host Gene & Cell Engineering Virtual Summit

GenScript to Host Gene & Cell Engineering Virtual Summit
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GenScript Launches Research-Grade Lentiviral Vector Packaging Service

Share this article Share this article PISCATAWAY, N.J., April 28, 2021 /PRNewswire/ GenScript®, the world s leading reagents provider, announced today the launch of its Research Lentiviral Vector Packaging Service for cell line development, gene editing, and drug discovery. The service enables scientists to package their genetic material of choice using GenScript s proprietary platform to ensure consistent production of functional and intact viruses. Lentiviruses in Cell Engineering Access to high volume, high quality lentiviruses has become increasingly important in identifying therapeutics to fight COVID-19 and mutant strains of the virus as they emerge. Dr. Nevan Krogan, a molecular and systems biologist who leads The Krogan lab at the Quantitative Biosciences Institute (QBI) at UCSF and the Gladstone Institute of Data Science and Biosciences (GIDB), is using GenScript s lentiviruses to identify drugs against COVID-19.

GenScript Biotech BV and IES Diagnostics Forge Distribution Agreement for SARS-CoV-2 Neutralizing An

Exclusive agreement for region brings GenScript s innovative cPass™ kit to Spain, Portugal and Andorra LEIDEN, Netherlands & BILBAO, Spain (BUSINESS WIRE) GenScript Biotech (Netherlands) BV, a subsidiary of GenScript Biotech Corporation ( GenScript , Stock Code: 1548.HK), a world-leading biotechnology company, and IES Diagnostics, the Life Science division of IES Medical, a company based in Spain, announced they have signed an agreement for the exclusive distribution of the GenScript cPass™ SARS-CoV-2 Neutralization Antibody Detection Kit in Spain, Portugal, and Andorra. The test measures the presence of neutralizing antibodies (NAbs) in patients recovering from COVID-19 or receiving a vaccine. It is the only U.S. FDA Emergency Use Authorized (EUA) serology test for neutralizing antibodies from recent and prior SARS-CoV-2 infections. The kit is also CE marked (Europe) and has received HSA provisional approval (Singapore), ANVISA in Brazil, ANMAT in Argentina and has recently re

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