ITGen Babesia Gibsoni Antigen Rapid Test
This product is suitable for clinical diagnosis in pet hospitals, disease screening in kennels, and blood protozoan infection monitoring in stray animal rescue stations. Babesia Gibbsoni is an important blood parasite transmitted by ticks, which can cause hemolytic anemia and even death in dogs. Traditional microscopic examination is time-consuming and relie

Product Parameters Production Name ITGen Babesia Gibsoni Antigen Rapid Test Target Analyte Babesia Gibsoni Antigen Specimen Type whole blood, serum or plasma sample Storage Temperature 4-30°C Result Time 5-10 Minutes Packaging Individually Sealed Tests Packaging Specification 10T Shelf Life Up to Expiration Date Indicated on Package Product Specifications Sensitivity 98% Accuracy 97.37% Format Cassette Detection Method Chromatographic Immunoassay/Lateral Flow Immunoassay Specificity 97.45% Reading Time 5-10 Minutes Usage Veterinary Diagnostics Contents Contents Number Test device 1 Quantitative dropper 1 Buffer tube 1 Package insert 1 Description The ITGen Babesia Gibsoni Antigen Rapid Test uses colloidal gold immunochromatography (GICA) to rapidly detect Babesia Gibbsoni antigens in whole blood based on the principle of double antibody sandwich.
During operation, you only need to drop the sample into the sample well, and the result can be interpreted by T/C line color development in 5-10 minutes. How to use? Check the product contents and make sure the test operation is under the room temperature (15–30℃) before testing.
Unseal the extraction tube containing the buffer.Place the extraction tube in the workstation. Squeeze the upper air bag to absorb the sample (whole blood/serum/plasma) . Please make sure some sample getting into the lower air bag and there is no bubbles in the lower tube.
Then press the upper air bag to transfer the sample (about 75 μl) left in the lower tube into the buffer. Cover the tube, Jiggle the extraction tube until the specimen and the buffer are mixed completely. Take the test device out of the aluminum foil bag, and place it on a clean, flat table.
Add three drops (about 90 μL) of the mixed sample vertically into the specimen well (S) of the test device. INTERPRETATION OF RESULTS Positive (+): The presence of both C line and T line, regardless of T line being strong or faint. Negative (-): Only clear C line appears. Invalid: No colored line appears in C region, regardless of T line’s appearance.
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