Antigen Rapid Collection Kit (Colloidal Gold)-for Swab
Antigen Rapid Collection Kit (Colloidal Gold)-for Saliva
COVID-19 Antigen Rapid Test Kit (colloidal gold)is used for in vitro qualitative detection of the antigen of novel corona virus in human throat swabs or nasal swabs.
Products Description
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Descripition
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Antigen rapid test kit-for saliva |
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Packing
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20 test/box, 400test/carton
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Testing time
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15 mins
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valid
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24 months
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Product Name |
Antigen rapid test kit-for swab |
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Testing content |
Detect the proteins of the virus |
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Test samples |
Nasal or throat swab |
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Detection time |
15 minutes |
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Usage |
Self-test |
* Composition
The test contains a membrane strip coated with Mouse anti-Human IgM antibody and Mouse anti-Human IgG antibody on the test line, goat anti rabbit IgG on the control line, and a dye pad which contains colloidal gold coupled with recombinant T. gondii antigens / Rubella antigens / Cytomegalovirus antigens / Herpes simplex virus 1/2 antigens and colloidal gold coupled with rabbit IgG. Materials required but not provided: Specimen collection container, Timer.
* Storage and Stability
* Store as packaged in the sealed pouch at room temperature (4-30℃ or 40-86℉).The kit is stable within the expiration date printed on the labeling.
* Once open the pouch, the test should be used within one hour. Prolonged exposure to hot and humid environment will cause product deterioration.
* Specimen
The test can be used to test Whole Blood /Serum / Plasma specimens.
* Collect blood specimen (containing EDTA, citrate or heparin) by veinpuncture following standard laboratory procedures.
* Separate the serum or plasma as soon as possible by centrifugation after collecting.
* Store specimens at 2-8℃ (36-46℉) if not tested immediately. Store specimens at 2-8℃ up to 7 days. The specimens should be frozen at -20℃(-4℉) for longer storage.
* Avoid multiple freeze-thaw cycles. Prior to testing, bring frozen specimens to room temperature slowly and mix gently. pecimens containing visible particulate matter should be clarified by centrifugation before testing.
* Do not use samples demonstrating gross lipemia, gross hemolysis or turbidity in order to avoid interference on result interpretation.
* Test Procedure
Allow the test device and specimens to equilibrate to room temperature (15-30℃ or 59-86℉) prior to testing.
1. Remove the test cassette from the sealed pouch.
2. Hold the dropper vertically and transfer 1 drop (approx. 10ul) of specimen to the "S" well of the test cassette, then add 2 drops of buffer (approximately 70ul), and start the timer. See the illustration below.
3. Wait for colored lines to appear. Interpret the test results in 15 minutes. Do not read results after 20 minutes.
* Components
Swab Version: Antigen extraction tube (with antigen extraction solution)oral or nasal swab, Test Cassette.
Saliva Version: Antigen extraction tube(with antigen extraction solution) oval funnel, Test Cassette.
* Other rapid test available
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Infectious disease test kits |
hepatitis test, HIV test, syphilis test, malaria test, Chlamydia test, gonorrhea test, h.pylori test, toxoplasma test, dengue test, typhoid test, torch test, tuberculosis test etc |
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Women health test kits |
pregnancy test, ovulation test, vaginal ph test |
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DOA drug of abuse test kits |
Morphine, opiate, cocaine , amphetamine/methamphetamine, ketamine, marijuana, ecstasy, barbiturates , methadone , benzodiazepine, phencyclidine test |
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tumor markers test kits |
PSA test ,FOB test, CEA test, AFP test |
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cardiac markers test kits |
myoglobin test, troponin I test,CK- MB test |
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alcohol test kits |
saliva alcohol test, urine alcohol test, milk alcohol test |
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urinalysis reagent test strips |
protein, glucose, ketene, ph and so on |
How to use
【INTERPRETATION OF RESULT】
1. Negative: If there is only a red line in the quality control area (C), indicating that 2019-nCoV antigen has not been detected and the result is NEGATIVE.
2. Positive: If both red reaction lines appear in the detection area (T) and the quality control area (C), indicating that 2019-nCoV antigen has been detected and the result is POSITIVE.
3. Invalid: When there is no red line in the quality control area (C), the test is invalid regardless of whether there is red line in the detection area (T) (as shown in the figure below). It is recommended to retest with a new test cassette, paying particular attention to whether the sample volume is sufficient.
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