PACKAGE SPECIFICATION
20 tests/kit, 40 tests/kit.
INTENDED APPLICATION
Immunochromatographic rapid assay for the Detection of Rotavirus Antigens in
Human Stool Specimens The test results are intended to aid in the diagnosis of rotavirus infection and to monitor the effectiveness of therapeutic treatment.
TEST PRINCIPLE
The test is a sandwich solid phase immunochromatographic assay. To perform the test, an aliquot of diluted stool sample is added to the sample well of the test card. The sample flows through a label pad containing rotavirus antibody coupled to red-colored colloidal gold. If the sample contains rotavirus antigens, the antigen will bind to the antibody coated on the colloidal gold particles to form antigen-antibody-gold complexes. These complexes move on the nitrocellulose membrane by capillary action toward the test line area on which rotavirus specific antibodies are immobilized. As the complexes reach the test line, they will bind to the antibody on the membrane in the form of a line. A second red control line will always appear in the result window to indicate that the test has been correctly performed and the test device functions properly. If rotavirus antigen is not present or lower than the detection limit of the test, only the control line will be visible. If the control line has not developed, the test is invalid.
MAIN COMPONENTS
20 tests/kit 40 tests/kit
Test card 20pcs 40pcs
sample collection bottle (1ml buffer contained) 20 pcs 40 pcs
Instruction 1pcs 1pcs
SUCCESSIVE OPERATING PROCEDURES
1) Before using the kit,you must read this introduction,and make sure that the kit and samples were returned to room temperature.
2) Open the sample collection bottle which has contained stool collection buffer, take one mung bean sized (about φ 5 mm) stool sample using a wooden stick, then put it into the sample collection bottle , cover back and screw up. Squeeze and shake the bottle thoroughly and finally keep resting for 2 minutes.
3) Take out one test card and make sure it should be used within 30 minutes. The card should be put on the clean, dry, flat test stand. Break off the top part of the bottle. Drop 2-3 drops sample extract into the sample well (S).
4) Read the result in 10 minutes. A strong positive sample may show result earlier. The result is not valid after 20 minutes.
PERFORMANCE INDICATORS
Positive compliance rate: ≥99%;
Negative compliance rate: ≥99%;
Intra batch discrepancy: ≤1%;
Inter batch discrepancy: ≤1 %.
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