Fluorescence Immunoassay Covid-19 Igg/Igm

Product code: SC-1309-20

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Fluorescence Immunoassay Covid-19 Igg/Igm – Product code: SC-1309-20

Immunofluorescence test for the qualitative detection of IgG and IgM antibodies to Sars-CoV-2 present in human whole blood, serum or plasma with the use of the Immunofluorescence Analyzer as an aid in the diagnosis of Covid-19 infection. For professional in vitro diagnostic use only. The Covid-19 IgG/IgM Cassette Test is an immunofluorescence test for the qualitative detection of Sars-CoV-2 IgG and IgM antibodies in whole blood, serum or plasma samples. The Covid-19 IgG/IgM test is an aid in diagnosing patients with suspected Sars-CoV-2 infection along with medical history and other laboratory test results. COVID-19 IgG/IgM test results should not be used as the sole basis for diagnosis. The results detect SARS-CoV-2 antibodies. The IgM antibodies of SARS-COV-2 are generally detectable in the blood several days after the onset of infection, even if the levels during the infection are not well determined. The IgG antibodies of SARS-COV-2 become detectable later in the course of the infection. Positive results for both IgG and IgM may occur following infection and indicate acute or recent infection. Negative results do not rule out SARS-CoV-2 infection and should not be used as the sole basis for patient management decisions. IgM antibodies may not be detected in the first few days of infection; the sensitivity of the COVID-19 IgG/IgM test in the early stages of infection is not known. False positive results for IgG and IgM antibodies may occur due to cross reactivity with pre-existing antibodies or other possible causes. At the moment, the duration of the persistence of IgM and IgG antibodies following infection is not known. The new coronavirus (SARS-CoV-2) belongs to the β genus. COVID-19 is an acute respiratory infectious disease. It mainly affects humans. Patients infected with the new coronavirus are currently the main source of infection; even asymptomatic infected individuals can be a source of infection. According to the latest epidemiological studies, the incubation period ranges from 1 to 14 days, and is mainly concentrated between the 3rd and 7th day. The most common manifestations include fever, fatigue, and dry cough. Nasal congestion, runny nose, sore throat, myalgia, and diarrhea are also present in some cases. The COVID-19 IgG/IgM Cassette Test (Whole Blood/Serum/Plasma) is a membrane-based, qualitative fluorescence immunoassay for the detection of SARS-CoV-2 IgM and IgG antibodies on whole blood, serum samples. or plasma. During testing, the sample containing IgG and / or IgM antibodies to SARS-CoV-2 reacts with SARS-CoV-2 antigens conjugated with fluorescent particles on the absorbent pad of the test cassette. The compound then migrates chromatographically on the membrane upwards by capillary action and reacts with the anti-human IgG and / or IgM antibody in the area of ​​the IgG and / or IgM test line of the NC membrane. The concentration of IgG and / or IgM SARS-CoV-2 in the sample is equal to the intensity of the fluorescent signal captured on the Test line, read by the SCREEN® Immunofluorescence Analyzer. The result of the COVID-19 IgG/IgM Test will appear on the screen of the SCREEN® Immunofluorescence Analyzer.


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