Fiv Ab Felv AG The Feline Immunodeficiency Virus Antibody Leukemia Viru Antigen Combo Rapid Test Kit

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HANGZHOU IMMUNO BIOTECH CO., LTD.

VIP   Audited Supplier 6 years
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JCA104D
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15cm*10cm*8cm
80 Box Per Carton
68cm*44cm*44cm
T/T, Western Union, Paypal
PETX
Carton
10 test per box
China
3822001000
Product Description
  • INTENDED USE
  • The FIV Ab/FeLV Ag Combo Rapid Test is a combined cassette to differentially diagnose the presence of Feline Immunodeficiency antibody and Feline Leukemia Virus antigen in cat's blood specimen.
    Assay Time:  5-10 minutes
    Specimen: Serum, plasma or whole blood
  • PRINCIPLE
  • The FIV Ab/FeLV Ag Combo Rapid Test is based on sandwich lateral flow immunochromatographic assay.
  • REAGENTS AND MATERIALS
  • Test devices
  • Disposable capillary droppers 
  • Assay buffers for FIV and FeLV assay
  • 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.
  • 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.
  • 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.
  • 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
  • The FIV Ab/FeLV 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 Western Blot when positive result was observed.


J&G Biotech Ltd (Reg. No.: 08419172)
326 Cleveland Road, London, England E18 2AN, UK

 
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