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Chinese Journal of Biotechnology ; (12): 953-957, 2007.
Article in Chinese | WPRIM | ID: wpr-276181

ABSTRACT

Specific primers and TaqMan MGB probes were designed with Primer Express 2.0 software according to the conserved region of the H5, H9, H7 subtype AIV hemagglutinin gene to make research of real-time fluorescent one-step PCR in the differential detection of H5, H9, H7 subtype avian influenza inactivated vaccines. The result showed that the method was specific and reproducible. No cross-reaction was discovered with other avian disease vaccines. Real-time fluorescent PCR provided a specific, sensitive, rapid and convenient method for the subtype identification of avian influenza inactivated vaccines.


Subject(s)
Animals , Humans , Hemagglutinin Glycoproteins, Influenza Virus , Allergy and Immunology , Influenza A Virus, H5N1 Subtype , Allergy and Immunology , Influenza A Virus, H7N7 Subtype , Allergy and Immunology , Influenza A Virus, H9N2 Subtype , Allergy and Immunology , Influenza A virus , Classification , Allergy and Immunology , Influenza Vaccines , Classification , Reverse Transcriptase Polymerase Chain Reaction , Methods , Vaccines, Inactivated
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