Canine respiratory tract Combined Detection (4 items)


Product Detail

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Packaging Details

Canine Distemper Virus (CDV) belongs to the genus Measles virus of the Paramucosal virus family, which can cause the spread of canine virulent infectious diseases (canine distemper) and lead to clinical phenomena such as conjunctivitis, pneumonia and gastroenteritis in dogs, etc. Canine distemper virus is characterized by high mortality, strong infectivity and short course of disease. Especially among puppies, there is a higher rate of infection and death.
Canine adenovirus type II can cause infectious laryngotracheitis and pneumonia symptoms in dogs. Clinical features include persistent high fever, cough, serous to mucinous rhinorrhea, tonsillitis, laryngotracheitis, and pneumonia. From the clinical incidence statistics, the disease is more common in puppies under the age of 4 months. Litter - or group-wide cough can be caused in puppies, so the disease is often called "kennel cough" according to clinical characteristics.
Canine influenza is mainly caused by influenza A virus types mainly H3N8 and H3N2. The initial symptoms are very similar to kennel bronchitis. It starts with a persistent cough that can last up to three weeks and is accompanied by a yellow nasal discharge.
Reliable and effective detection has a positive guiding role in prevention and diagnosis and treatment.

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Detection Principle

The product was used for quantitative detection of CDV/CAV-2/FluA Ag in canine eye, nose and mouth secretions by fluorescence immunochromatography. Basic principle: The nitro fiber membrane is marked with T and C lines respectively, and the T lines are coated with antibodies a1, a2 and a3 that specifically recognize CDV/CAV-2/FluA antigens. Antibodies b1, b2 and b3 labeled with another fluorescent nanomaterial that can specifically recognize CDV/CAV-2/FluA were sprayed on the binding pad. CDV/CAV-2/FluA in the sample first combined with the nanomaterial labeled antibodies b1, b2 and b3 to form a complex, and then went to the upper layer. The complex is combined with T-line antibodies a1, a2 and a3 to form a sandwich structure. When the excitation light is irradiated, the nanomaterial emits a fluorescence signal, and the strength of the signal is positively correlated with the dependent virus concentration in the sample.


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