- Canine Influenza Virus Antigen Rapid Test
-
- INTENDED USE
- The Canine Influenza Virus Antigen Rapid Test is a lateral flow immunochromatographic assay for the qualitative detection of canine Influenza virus antigen (CIV Ag) in secretions from dog's eyes, nasal cavities, and anus or in serum, plasma specimen.
Assay Time: 5-10 minutes
- PRINCIPLE
- The Canine Influenza Virus Antigen Rapid Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window for the observation of assay running and result reading. The testing window has an invisible T (test) zone and a C (control) zone before running the assay. When the treated sample was applied into the sample hole on the device, the liquid will laterally flow through the surface of the test strip and react with the pre-coated monoclonal antibodies. If there is CIV antigen in the specimen, a visible T line will appears. The C line should always appear after a sample is applied, which indicates a valid result. By this means, the device can accurately indicate the presence of Influenza virus antigen in the specimen.
- What are the symptoms of canine influenza?
- Canine influenza is a contagious disease caused by the canine influenza virus. Symptoms of canine influenza include coughing, sneezing, clear nasal discharge, fever, sore throat, loss of appetite, and fatigue. Canine influenza is primarily spread through direct contact between dogs or through airborne respiratory droplets. Prevention measures include vaccination, avoiding close contact between dogs, and maintaining good hygiene practices.
- Advantage:
- Precise: high accuracy, the accuracy rate can reach 98%.
· Rapid: just 15 mins to read the test result.
· Convenient: the test can be performed anytime, anywhere.
· Privacy protection: at-home testing and can protect privacy of customer.
- REAGENTS AND MATERIALS
- Test devices, with disposable droppers
- Assay buffer
- Cotton swabs
- Products Manual
- STORAGE AND STABILITY
- 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.
- TEST PROCEDURE
- Collect dog's ocular, nasal or anus secretions with the cotton swab and make the swab wet sufficiently.
- Insert the swab into the provided assay buffer tube. Agitates it to get efficient sample extraction.
- Take out the test device from the foil pouch and place it horizontally.
- Suck the treated sample extraction from the assay buffer tube and place 3 drops into the sample hole "S" of the test device.
- 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.
- PRECAUTIONS
- 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.
- LIMITATION
- Canine Influenza Virus Antigen 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 RT-PCR when positive result was observed.
J&G Biotech Ltd (Reg. No.: 08419172)
326 Cleveland Road, London, England E18 2AN, UK
Company Profile
Hangzhou Immuno Biotech Co., Ltd is the original organization in IMMNUO Group, which was established in 2014. The team of Hangzhou Immuno Biotech has developed a series of proteins and rapid test kits for the in vitro diagnostic industry in early stage. Gradually, IMMUNO was well known as a good R&D partner and good supplier of veterinary rapid test products. With great patience and continuous investment in design and development of IVD relative reagents and test kits, we got several encouraging achievements in the past year, especially in veterinary diagnostic field.
To achieve that goal, IMMUNO has decided to focus on the development of rapid testing tools for zoonosis diseases and formed a joint action within our group. Now, we have a scientific team to analyse and develop recombinant proteins and antibodies, a technical team to apply the proteins and antibodies to immunoassay format, and also a joint team to study the diseases themselves and their possible application scenarios.
Hangzhou Immuno Biotech Co., Ltd. will focus on the human medical diagnostic field and mainly cover the following directions: rapid tests for vector-borne diseases(VBDs), rapid tests for sexually transmitted diseases (STDs), rapid tests for respiratory system diseases and rapid tests for digestive system diseases. Besides, with strong R&D capability, we would pay more attention to the diagnosis of neglected tropical diseases (NTDs).
IMMUNO will continuously contribute to the development of diagnostic tools for the whole human society and nature world.
Audited Supplier 
Audited Supplier 
){kind=link}
){kind=link}