Sale! Veterinary Rapid Test-- Peste Des Petits Ruminants Test Kit (PPR Penside) for Veterinary

Basic Info

Model NO.	JCA018D
Type	Detection Card
for	Canine
Assay Time	5-10 Minutes
Accuracy	98%
Shelf Life	24 Months
Storage Temperature	2-30 Degree
Certificate	ISO9001
OEM/ODM	Support
Specification	10Test/Kit
Trademark	PETX
Origin	Hangzhou
HS Code	3822001000
Production Capacity	5000000PCS/Year

Product Description

Peste des Petits Ruminants Test Kit(PPR Penside)

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
Specime	Serum, secretions or spleen
Storage	4 to 30 degree centigrade
Shelf life	18 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

INTENDED USE

The PPR Penside Test Kit is a rapid test for the detection of PPR virus. It is an immuno-chromatographic assay for the qualitative diagnosis of Peste des Petits Ruminants Virus Antibody (PPR Ab) in sheep's serum or plasma specimen.Assay Time: 10-15 minutesSpecimen: serum or plasma.

PRINCIPLE
The PPR Penside Test Kit 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 PPR antigens. If there are anti-PPR antibodies 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 Bovine Brucella antibodies in the specimen.

Test Procedure

• Collect sheep's fresh whole blood, get the serum or plasma specimen for use. Immediately apply the testing once collected the specimen. If not use right now, keep storage at 2-8°C. If the storage time more than 24hours, the specimen should be frozen at -20°C.
• Take the test kit to room temperature (20-30°C) before use. Keep all component in room temperature for at least 30 minutes to recover the reaction conditions.
• Take out the test device from the foil pouch and place it horizontally.
• Place 4 drops (approx. 120μL) of serum or plasma specimen into the sample hole of the test card.
• Interpret the result at 10 minutes. Result after 15minutes is considered as invalid.

Quality Control
J&G Biotech, pays much attention to product quality and design success rate. On the premise of guaranteeing high supply efficiency , all the products supplied by J&G Biotech are of high and steady quality. We are running ISO9001 and ISO13485 quality control systems to ensure the good quality of our products. Owing to its professional quality and high-quality services , J&G Biotech gradually establishes a good reputation in the industry . However, J&G Biotech is not satisfied with its present achievements . Adhering to the excelsior spirit , J&G Biotech keeps enhancing development strength , with a view to providing better products to customers.

Our Service

1. Factory price, reasonable and competitive

2. OEM/ODM service, Not only packaging and brand customization, we have our own laboratory and R&D team, which can develop and customize proprietary products for customers

3. Timly and quickly feedback, anytime and anywhere for customer service.

4. Provide professional training and quality samples to help customers develop the market

5. Flexible trading methods to meet customer and business needs

Logistics

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