Human Chorionic Gonadotropin Detection Kit (Colloidal Gold Method)

Human Chorionic Gonadotropin Detection Kit (Colloidal Gold Method)

As the professional manufacture, we would like to provide you Human Chorionic Gonadotropin Detection Kit (Colloidal Gold Method). And we will offer you the best after-sale service and timely delivery.

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Product Description

INTENDED USE
The Pregnancy test intended use of the reagents used in vitro qualitative urine testing women in human chorionic gonadotropin detection kit (colloidal gold method), auxiliary diagnosis for the early weeks of pregnancy.
This early pregnancy test is only provided for use by clinical laboratories or to health care workers for point of care testing, and not for at home testing.
Results from antigen testing should not be used as the sole basis to diagnose or exclude pregnancy. The hcg test diagnosis should be confirmed in combination with clinical symptoms or other conventional testing methods.

SUMMARY AND EXPLANATION OF THE TEST

Human chorionic gonadotropin is a glycoprotein secreted by the trophoblast cells of the placenta. The examination of HCG is of great significance for the diagnosis of early pregnancy.


TEST PROCEDURE
1. Open the packaging box, take out the inner package and let it equilibrate to room temperature.
2. Remove the test card from sealed pouch and use within 1 hour after opening. 3. Place the test card on a clean and level surface.
4. When testing the test strip, vertically immerse the test end of the test strip in the urine cup containing urine until the mark line is reached. After at least 3 seconds, take it out and place it on a flat surface.
5. When the test card is tested, use a straw to suck urine and add 2-3 drops to the sample port of the test card.
6. The start time, 5-15 minutes, 15 minutes after the decision is invalid.
INTERPRETATION OF ASSAY RESULT
1. NEGATIVE:
If only the quality control line C appears, and the test lines T are not burgundy, it indicates that no HCG is detected, and the result is negative. Due to the limitation of detection sensitivity, negative results may be caused by HCG concentrations lower than the analytical sensitivity of the product.
2. POSITIVE:
If both the quality control line C and the test line T appear , it indicates that HCG is detected.Samples with positive results should be confirmed with alternative testing method(s) and clinical findings before a diagnosis is made.
3. INVALID:
If the quality control line C is not displayed, the test result is invalid regardless of whether there is a burgundy test line, and it should be tested again. Repeat the test using remaining sample or new sample, if results are not clear. If the test repeated fail to produce a result, discontinue using the kit and contact the manufacture.



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