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    Serology

    FDA authorizes initial two COVID-19 serology tests

    Today, the U.S. Food and Drug Administration approved the initial two COVID-19 serology tests which show an estimated amount of antibodies within somebody’s blood. Both tests from Siemens, the ADVIA Centaur COV2G and Attelica COV2G are what are known as”semi-quantitative” evaluations, meaning that they don’t show an exact measurement, but estimate the number of a

    Covid-19 Antibody Rapid Serology Test by Americal Screening

    American Idol, Shreveport, La, has included a covid-19 IgG/IgM rapid test to its inventory. The in vitro immunoassay, that has been allowed emergency use authorization (EUA) from the FDA, is created for the qualitative and direct discovery of anti-SARS-CoV-2 IgM and anti-SARS-CoV-2 IgG in human whole blood, serum, or plasma. The test is simple to