Fiv Ab+Felv AG+Heartworm AG Combo Rapid Test (FIV-FELV-HW)
Canine Antigen Rapid Test
| Principle |
Immunochromatographic assay |
| Intended use |
Veterinary in vitro diagnostic
1) Auxiliary diagnosis on Canine infection for veterinarians in practice.
2) Precautionary diagnosis for home use, point-of-care and early judgement for pet owners.
3) Study use for researchers. |
| Detection time |
5 to 10 minutes |
| Specimen |
According to the instruction for use |
| Storage |
4 to 30 degree centigrade |
| Shelf life |
24 months |
| Package |
10 rapid tests
10 sterile swabs
10 assay buffer
1 package insert |
| Advantages |
1) Good sensitivity and specificity
2) Strong R&D and technical support
3) Stable performance.
4) Friendly to end users |
| Relative products |
- Canine CPV-CCV Combo Test
- Giardia Antigen Test |
The FIV Ab/FeLV Ag/Heartworm Ag Combo Rapid Test is a test cassette to diagnose the presence of antibodies against Feline Immunodeficiency antibody,Feline Leukemia Virus antigen,Heartworm Antigen in cat's blood specimen.
Assay Time: 5-10 minutes
The FIV Ab/FeLV Ag/Heartworm Ag Combo Rapid Test is based on sandwich lateral flow immunochromatographic assay.
- Test devices
- Disposable capillary droppers
- Assay buffers
- Products Manual
The kit can be stored at room temperature (4-30°C). The test kit is stable through the expiration date (24 months) marked on the package label. DO NOT FREEZE. Do not store the test kit in direct sunlight.
- SPECIMEN PREPARATION AND STORAGE
- Specimen should be obtained and treated as below.
- Serum or plasma: collect the whole blood for the patient cat, centrifuge it to get the serum, or place the whole blood into a tube which contains anticoagulants to get plasma.
- Whole blood: collect fresh blood for use directly or make anticoagulant blood for storage at 2-8ºC.
2. All specimen should be tested immediately. If not for testing right now, they should be stored at 2-8ºC.
- Allow all materials, including specimen and test device, recover to 15-25ºC before running the assay.
- Take out the test device from the foil pouch and place it horizontally.
- Using the capillary dropper to place 10μL of the prepared specimen into the sample hole "S" of the test device. Then drop 3 drops (approx. 90μL) of the assay buffer into the sample hole immediately.
Interpret the result in 5-10 minutes. Result after 10
- minutes is considered as invalid.
- INTERPRETATION OF RESULTS
- Positive (+): The presence of both "C" line and zone "T" line, no matter T line is clear or vague.
- Negative (-): Only clear C line appear. No T line.
- Invalid: No colored line appears in C zone. No matter if T line appears.
- All reagents must be at room temperature before running the assay.
- Do not remove test cassette from its pouch until immediately before use.
- Do not use the test beyond its expiration date.
- The components in this kit have been quality control tested as standard batch unit. Do not mix components from different lot numbers.
- All specimens are of potential infection. It must be strictly treated according to the rules and regulations by local states.
The FIV Ab/FeLV Ag/Heartworm Ag Combo Rapid Test is for in vitro veterinary diagnosis use only. All result should be considered with other clinical information available with veterinarian. It is suggested to apply a further confirmative method such as PCR when positive result was observed.
J&G Biotech Ltd (Reg. No.: 08419172)
326 Cleveland Road, London, England E18 2AN, UK
Audited Supplier 
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