Produced by
Country of origin
Russian Federation
Detects
Antigen
Biomaterial
Nasopharyngeal swab
Rapid Bio COVID-19 IgM/IgG
98%
Specificity
96%
Sensitivity
20 minutes - ready time
Helps in confirming the diagnosis
Easy to use, no laboratory equipment required
Product overview
Express Antigen SARS-CoV-2-ICA is a reliable lateral flow test for detecting SARS-CoV-2 antigen in a sample (human nasopharyngeal swab). The test works based on an immunochemical method for detecting antigens using immunoglobulins. The sample is absorbed by the stripe material, and the antigen within it reacts with colored microparticles covered with a special antibody.
Kit contains:
Kit No1:
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Test cartridge for detecting SARS-CoV-2 antigens – 20 pcs.
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Dropper bottle with buffer solution – 1 pc.
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Микроцентрифужная пробирка – 20 шт.
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Plastic pipette — 20 pcs.
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Usage instructions — 1pc.
Kit No2:
-
Test cartridge for detecting SARS-CoV-2 antigens – 20 pcs.
-
Dropper bottle with buffer solution – 1 pc.
-
Plastic tube with dropper cap — 20 pcs.
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Usage instructions — 1pc.
Kit No3:
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Test cartridge for detecting SARS-CoV-2 antigens – 1 pc.
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Monodose with buffer solution — 1 pc.
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Microcentrifuge tube — 1pc.
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Plastic pipette — 1 pc.
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Usage instructions — 1pc.
Kit No4:
-
Test cartridge for detecting SARS-CoV-2 antigens – 1 pc.
-
Monodose with buffer solution — 1 pc.
-
Plastic tube with dropper cap — 1pc.
-
Usage instructions — 1pc.
Materials not included
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Nasopharyngeal swabs with plastic applicator for collecting biomaterial sample (respiratory secretions from nasopharynx);
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timer or stopwatch;
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personal protective equipment.
Use order
Biomaterial sampling
Adding 10 μL of sample to the well
Expect the result according to the time in the instructions
Interpreting the rapid test results
If the (C) line turns red:
The test returned a negative result for the presence of coronavirus antigen.
If the (C) line turns red and the (T) line turns black:
The test returned a positive result for the presence of coronavirus antigen.
If the (C) line in the window does not turn red:
The test result is invalid. Possible causes could include non-compliance with biological sample collection requirements, and/or analysis procedures, or the test system used is faulty.