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Thermo Fisher Scientific to Acquire PPD, Inc , a Leading Clinical Research Organization
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Genomic Vision appoints Mark David Lynch as Global Commercial and Marketing Director
(Paris:GV)
(the Company FR0011799907 GV), a biotechnology company that develops tools and services dedicated to the analysis and control of changes in the genome, today announces the appointment of Mark David Lynch as Global Commercial and Marketing Director.
Graduated in microbiology from University of Glasgow, Mark David Lynch has extensive experience in the business development of research and diagnostic devices.
Prior to joining Genomic Vision, Mark spent nearly 10 years at Fluidigm Corporation, a US biotechnology company, where he held different senior management positions, before becoming Head of Sales Support. He was instrumental in the Company s expansion, with substantial contribution to the growth of its microfluids business in the US market in 2020. During his career at Fluidigm, Mark has received several performance-related company awards.
Genomic Vision appoints Mark David Lynch as Global Commercial and Marketing Director
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Cell Lines
ESCC cell lines (Eca109, KYSE150, KYSE180 and KYSE450) and human esophageal epithelial cell line HET-1A were purchased from the Shanghai Institute of Chinese Academy of Sciences Cell Collection (Shanghai, China). All these five cell lines were cultured with Roswell Park Memorial Institute-1640 medium (RPMI-1460; Gibco, Carlsbad, CA, USA) added with 10% fetal bovine serum (FBS; Gibco), 1% 100 units/mL penicillin (Gibco) and 1% 100 μg/mL streptomycin (Gibco). All cell lines were maintained at 37°C incubator with 5% CO
2.
Western Blot Assay
ESCC cells were collected and lysed using whole cell lysis buffer (Abcam). Protein quantification was conducted with the commercial bicinchoninic acid (BCA) protein assay kit (Invitrogen, Carlsbad, CA, USA). Proteins were separated using sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) gel and transferred onto the polyvinylidene difluoride (PVDF) membrane (Millipore, Billerica, MA, USA). After blocking, the membra
FDA Authorizes New High-Throughput, Automated System for Leading COVID-19 Test
Thermo Fisher Scientific Inc. the world leader in serving science, today announced that the U.S. Food and Drug Administration has granted Emergency Use Authorization for the Thermo Fisher Scientific Amplitude Solution with the TaqPath COVID-19 High-Throughput Combo Kit. The Amplitude Solution enables clinical and public health laboratories to scale gold standard PCR testing and process up to 8,000 samples in a …
– Thermo Fisher Scientific Inc. (NYSE:TMO), the world leader in serving science, today announced that the U.S. Food and Drug Administration (FDA) has granted Emergency Use Authorization (EUA) for the Thermo Fisher Scientific Amplitude Solution with the TaqPath COVID-19 High-Throughput Combo Kit.
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