Canine Babesia Antibody 1.0 Rapid Test Babesia Blood Smear

• Customization: Available
• Type: Detection Card
• Syringe: None
• Model NO.: JCA033D
• Blood Sampling Needle: None
• Breathing Pattern: None
• Animal Anesthesia Machine Control Method: None
• for: Canine
• Assay Time: 5-10 Minutes
• Delivery Time: 3~5days After Get Payment
• Payment: T/T, Western Union, Paypal
• Transport Package: Carton
• Specification: 10Test/Kit
• Trademark: PETX
• Origin: Hangzhou
• HS Code: 3822001000
• Production Capacity: 5000000PCS/Year

Product Description

Canine Babesia Antibody 1.0 Rapid Test 

Principle	Immunochromatographic assay
Intended use	Veterinary in vitro diagnostic 1)Auxiliary diagnosis on Canine Babesia infection for veterinarians in practice.  2)Assess puppy immunity level and 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	serum or plasma
Storage	4 to 30 degree centigrade
Shelf life	24 months
Package	10 rapid tests  10 assay buffer 10 Sample collection loop 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	- EHR-ANA Combo Test (Ehrlichia-Anaplasma) - EHR-ANA-LYM-CHW Combo Test (Ehrlichia-Anaplasma-Lyme disease-Heartworm) - EHR-ANA-Bab gib Combo Test (Ehrlichia-Anaplasma-Babesia gibsoni) - EHR-ANA-Bab gib-CHW Combo Test (Ehrlichia-Anaplasma-Babesia gibsoni-Heartworm)

• Canine Babesia Antibody 1.0 Rapid Test Babesia gibsoni Ab
• INTENDED USE

The Canine Babesia Antibody 1.0 Rapid Test is a test cassette to diagnose the presence of Babesia gibsoni antibodies (Babesia gibsoni Ab) in dog's serum or plasma specimen.
Assay Time:  5-10 minutes
Specimen: Serum, plasma or Whole blood. 

• PRINCIPLE

The Canine Babesia Antibody 1.0 Rapid Test is based on sandwich lateral flow immunochromatographic assay. Babesia specific recombinant antigen was applied in this assay, specially combine the Babesia antibodies in specimen and form a visible line.

• REAGENTS AND MATERIALS

• Test devices
• Assay buffer
• Disposable capillary droppers
• 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 dog, 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.

• 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. 80μL) 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 Babesia Antibody 1.0 Rapid Test is for in vitro veterinary diagnosis use only. The test could not distinguish different Babesia species. Some Babesia canis may be reacting with the Babesia gibsoni test. 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.