Hightop Biotech SARS-CoV-2 IgM/IgG Antibody Rapid Test (1 Test)
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• For professional use.
Price: €4,56/pcs
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IgM/IgG antibody test introduction
The HIGHTOP BIOTECH SARS-CoV-2 IgM/IgG antibody rapid test kit is used to detect the IgM and IgG antibodies to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in human serum, plasma or whole blood sample qualitatively. It is to be used as an aid in the diagnosis of coronavirus infection disease (COVID-19), which is caused by SARS-CoV-2. For professional use.
Specification
Product name: SARS-CoV-2 IgM/IgG Antibody Rapid Test
Specimen: Whole Blood/Serum/Plasma
Kit size: 1 Test/Kit
Format: Cassette
Manufacturer: Hightop Biotech Co., Ltd.
Expiration date: 2023.11.24.
Certificates:
File number: OGYÉI/23612-3/2021
Registration number: HU/CA01/23612/21
Certificates
Instructions
Main components of the Covid-19 antibody test kit
- Test cassette
- Sample dilution
- Disposable plastic straw
- Sterile yellow lancet
- Alcohol pad
- Instructions
Covid-19 antibody rapid test methods
For whole blood:
1.
Remove the test cassette from the sealed pouch, place it on a clean and level surface with the sample well up. Add two (2) full drops of whole blood (20μ) vertically into the sample well.
2.
Add two (2) drops (80-100μ) of sample buffer into the sample well.
3.
Observe the test results immediately within 15~20 minutes, the result is invalid over 20 minutes.
For serum or plasma:
1.
Remove the test device from the sealed pouch, place it on a clean and level surface with the sample well up. Add one (1) full drop of serum or plasma (10 μ) vertically into the sample
2.
Add two (2) drops (80-100 μ) of sample buffer into the sample well.
3.
Observe the test results immediately within 15~20 minutes, the result is invalid over 20 minutes.
Lancet instructions
1.
Carefully pull off the protective cap.
2.
Push the safety lancet firmly onto the chosen site to fire.
3.
Throw it in a suitable container after use.
Interpretation of results
Positive
Two distinct red lines appear. One line should be in the control region (C) and another line should be in the (G) test region, indicating the lgG positive.
Positive
Two distinct red lines appear. One line should be in the control region (C) and another line should be in the (M) test region, indicating the lgM positive.
Positive
Three distinct red lines appear. One line should be in the control region (C), the (G) test region and the (M) test region, indicating the lgG and lgM positive.
Negative
One red line appears in the control region (C). No red or pink line appears in the test region (G, M).
Invalid
No red lines appear or control line fails to appear, indicating that the operator error or reagent failure. Verify the test procedure and repeat the test with a new testing device.
Invalid
No red lines appear or control line fails to appear, indicating that the operator error or reagent failure. Verify the test procedure and repeat the test with a new testing device.
Invalid
No red lines appear or control line fails to appear, indicating that the operator error or reagent failure. Verify the test procedure and repeat the test with a new testing device.
Invalid
No red lines appear or control line fails to appear, indicating that the operator error or reagent failure. Verify the test procedure and repeat the test with a new testing device.
Performance characteristics of the Covid-19 antibody rapid test
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