BC Ab

BC Ab

Product catalog summary
Intended Use
The Babesiosis Canine Antibody Rapid Test (BC Ab) is a lateral flow immunoassay designed for the qualitative detection of specific antibodies from Babesiosis Canine in canine whole blood, serum, or plasma samples. It aids in determining BC infection.
Specifications and Performance Characteristics
The test demonstrates a diagnostic sensitivity of 98.00% and a specificity of 96.67%, with a total agreement of 97.00%. It is intended for use in canines only, and results may be affected by humidity and temperature.
Test Procedure
1. Unseal the extraction tube containing the buffer and place it in the workstation.
2. Absorb the sample using the quantitative dropper and transfer it into the buffer.
3. Mix the specimen and buffer thoroughly.
4. Add three drops of the mixed sample into the specimen well of the test device.
5. Read the result within 5-10 minutes; results are invalid after 15 minutes.
Interpretation of Test Results
- Negative (-): Only the C line appears.
- Positive (+): Both C and T lines appear, regardless of the T line's intensity.
- Invalid: No colored line appears in the C region.
Limitations
While the test is accurate, false results may occur. Additional clinical or laboratory tests are recommended for questionable results. A definitive diagnosis should be made by a veterinarian after evaluating all clinical and laboratory findings.
Specimen Collection and Handling
- Whole blood, serum, or plasma can be used.
- Whole blood should be refrigerated if not tested immediately and used within 24 hours.
- Serum and plasma should be stored at 2-8°C, and samples can be frozen at -20°C for longer storage.
- Avoid using hemolyzed or contaminated samples as they may lead to erroneous results.
Storage and Stability
The test device should be stored at room temperature (4-30°C) away from light and used before the expiration date. Do not freeze the test device.
Warnings and Precautions
- Ensure the test pouch is not damaged before use.
- Do not reuse test components or use them after the expiry date.
- Handle all samples as potentially infectious and dispose of them safely according to regulations.
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Catalog excerpts

BC Ab-1

Babesiosis Canine Antibody Rapid Test(BC Ab) Intended Use Babesiosis Canine Antibody Rapid Test is a lateral flow immunoassay intended for the qualitative detection of specific antibody from Babesiosis Canine (BC) in canine whole blood, serum or plasma sample. The test is useful for determination of BC infection. Reagent and Materials Provided • Test devices • Quantitative droppers • Buffer tubes • Package insert Materials Required but not Provided Timer Storage and Stability The test device is sealed and should be stored away from light at a room temperature (4-30oC). Do not freeze. The test device should be used before the expiration date marked on the package label. Warnings, Precautions and Safety Information 1. The test device is used for canine only. 2. The results may be influenced by humidity and temperature. 3. Make sure that the foil pouch containing the test is not damaged before open. Perform the test immediately when the pouch package is opened. 4. Do not reuse the test components. 5. Do not use after the expiry date. 6. Do not mix product components in different lot numbers. 7. As all samples are potentially infectious. Operators should wear protective gloves while handling samples and wash hands thoroughly afterwards. 8. Decontaminate and dispose of all samples, used kits and potentially contaminated materials safely in accordance with national and local regulations. Specimen Collection, Handling, and Transport I.Whole blood, serum or plasma should be used with this test. Whole blood: Collect the whole blood. If whole blood samples are not immediately tested, they should be refrigerated at 2~8°C and used within 24 hours. Serum: Collect the whole blood into the collection tube (NOT containing anticoagulants such as heparin, EDTA and sodium citrate), and then centrifuge whole blood to get serum. Plasma: Collect the whole blood into the collection tube (containing anticoagulants such as heparin, EDTA and sodium citrate) and then centrifuge whole blood to get plasma. 2.Samples should be stored at 2~8°C. Please freeze the samples at -20°C or below for longer storage and avoid repeated freezing and thawing. 3. Samples containing precipitate may yield inconsistent test results. They must be clarified prior to assaying. 4. Hemolyzed or contaminated samples may lead to erroneous results. STEP 1 CHECK THE KIT CONTENTS BEFORE USE Check the product contents and make sure the test operation is under the room temperature (15—30C) before testing. STEP 2 TEST PROCEDURE 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 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 from the aluminum foil bag, and place it on a clean, flat table. Add three drops (about 90 pL) of the mixed sample vertically into the specimen well (S) of the test device. STEP 3 INTERPRETATION OF TEST RESULT Read the result at 5-10 minutes. The result is invalid after 15 minutes. 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. Although the Babesiosis Canine Antibody Rapid Test is very accurate in detecting Babesiosis Canine Antibody, a low incidence of false results may be occurred. Other clinically or laboratory tests might be required if questionable results are obtained. As other diagnostic tests, a definitive clinical diagnosis should not be based on the result of a single test, but should be diagnosed by the veterinarian after all clinical and laboratory findings have been evaluated. Performance Characteristics Method

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