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- One-step Canine Parvovirus Antigen Test for veterinary use
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(Whole Blood / Serum / Plasma / Milk)
●INTENDED USE
Canine Parvovirus Antigen Rapid Test Kit (whole blood/serum/plasma/milk) is a solid phase immunochromatographic assay for the rapid, qualitative and dfferentia ldetection of antibody to animal whole blood/serum/plasma/milk. This test provide only a preliminary analytical result. A secondary analytical method must be used to obtain a confirmed result. Gas chromatography and mass spectrometry (GC/MS) are the preferred confirmatory methods.
●PRINCIPLE
Canine Parvovirus Antigen Rapid Test Kit is based on the technology of colloidal gold immunochromatography assay. After the sample is added to the sample well, the liquid sample and colloidal gold marker are moving together along with chromatographic membrane. If Canine Parvovirus exists in the sample, the antibody is combined with it and the test line appears red. There is no color reaction when the testing sample has no Canine Parvovirus Virus.
●MATERIAL SUPPLIED
| No. | Name | 50T/Kit |
| 1 | Rapid Test Cassette | 50 Tests/Kit |
| 2 | Plastic Dropper | 50 Tubes/Kit |
| 3 | Buffer | 50 Bottles/Kit |
| 4 | Package Insert | 1 Set/Kit |
●STORAGE AND STABILITY
1. The kit can be stored at room temperature of 2-30℃.
2. The shelf life is 24 months. The test device is stable through the expiration date printed on the sealed pouch. The test device must remaing in the sealed pouch until use.
3. DO NOT FREEZE. Do not use beyond the expiration date.
●SAMPLE REQUIREMENTS
This test kit is only applicable to the detection of dog wastes.
●SPECIMEN COLLECTION
Canine Parvovirus Antigen Rapid Test Kit can be performed using eyes secretions, nasal fluid or saliva.
1. Use swabs to collect either eyes secretions, nasal fluid or saliva .
2. Unscrew the cap of bottle, insert the cotton swab into the bottle containing the buffer .
3. Apply the cotton swab against the tube wall and circle along the it at least 10 times to make buffer and sample fully mixed.
4. Squeeze the cotton swab against the tube wall to push the liquid out.
5. Discard the swab, cap and keep the tube still.
6. Suck 100ul (3 drops) of liquid supernatant to test.
●TEST PROCEDURE
Allow test cassete, specimen, and/ or controls to equilibrate to room temperature (15-30℃) prior to testing.
1. Remove the test cassette from the sealed foil pouch and use it as soon as possible.Best results will be obtained if the assay is performed within one hour.
2. Place the test device on a clean and level surface.
3. Add 100ul (3 drops) sample into the sample well.
4. Wait for the colored line(s) to appear. The result should be read at between 10-15 mintues. It is invalid after 15 minutes.
●READ RESULTS WITH NAKED EYES
NEGATIVE: If only the C band is present, it is negetive.
POSITIVE: In addition to the presence of C band, T band is developed, it is positive.
INVALID: Reference Line Fails to appear
Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for an invalid result. Review the procedure and repeat the test with a new test kit. Stop using the test kit immediately if the problem is not solved and contact your local distributor.
Bella@nkbiotech.com
Whatsapp: 0086-151-5809-6930
Tel.: 0086-151-5809-6930
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NANKAI Biotech develops and manufactures rapid testing solutions for real-world food safety risk control.
For more than 20 years, we have focused on fast, practical and reliable rapid screening technologies that help regulators, laboratories, distributors, exporters and food industry QC teams make faster food safety decisions.
NANKAI provides rapid screening and quantitative analysis solutions for pesticide residues, mycotoxins, illegal additives, aquaculture & seafood safety, veterinary drug residues, antibiotics, heavy metals & toxic elements, digital QC, traceability systems and related food safety applications.
What differentiates NANKAI is the combination of large-scale manufacturing, certified analytical laboratory verification and extensive real-world deployment experience.
We operate three CMA, CATL & CNAS certified analytical laboratories equipped with LC-MS/MS and GC-MS/MS platforms, supporting matrix verification, reference method comparison, rapid test performance evaluation and accredited third-party analytical testing services.
Our rapid testing solutions have been applied in Olympic-level food safety programs, major international events, government monitoring projects, grain & feed safety workflows, fruit & vegetable screening, tobacco & tea quality control, seafood and meat safety supervision, traditional herbal material testing, dairy and honey safety programs, factory QC and export risk-control workflows.
Highlights:
• Fast, practical and reliable rapid screening solutions
• 20+ years of rapid testing technology development
• 25,000+ m² manufacturing & laboratory facilities
• Three CMA, CATL & CNAS certified analytical laboratories
• LC-MS/MS & GC-MS/MS analytical capability
• Olympic-level and government project experience
• Billions of real-world screening applications
• Food safety monitoring, traceability and digital regulatory systems
NANKAI Biotech supports international partners with practical, scalable and laboratory-verified rapid testing solutions for food safety risk control.
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