Basic Info.
Model NO.
JCA103C
Customized
Accpet
Payment
T/T, Western Union, Paypal
Box Size
15cm*10cm*8cm
Packing
80 Boxs/Carton
Carton Size
68cm*44cm*44cm
Transport Package
Carton
Specification
10Tests/Kit
Trademark
PETX
Origin
Hangzhou
HS Code
38220010
Production Capacity
5000000PCS/Year
Product Description
Feline Immunodeficiency Virus Antibody Rapid Test fiv test
Canine Antigen Rapid Test
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 |
- TEST PROCEDURE
- 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.
- 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