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Clone | IHA-H3N2-PRS. |
Purity | 90%. |
Applications | Influenza A haemagglutinin H3N2 Western Blotting at a concentration of 0.5ug/ml. ELISA to be determined. |
Inactivation | Protein quantitation was carried out by UV spectroscopy at 280 nm using the absorbency value of 0.21 as the extinction coefficient for a 0.1% (1mg/ml) solution at pH 8.0. This value is calculated by the PC GENE computer analysis program of protein sequences (IntelliGenetics). |
Description | Influenza Hemagglutinin protein is an envelope glycoprotein responsible for binding to sialic receptors and influenza viral entry into host cells. The antibody was produced by immunization of rabbits with purified recombinant influenza A/Wisconsin/67/05 produced in insect cells using baculovirus expression vector system. The antigen was purified under conditions that preserve the HA proteins biological activity and tertiary structure. |
Protein Background | H3N2 is a subtype of the influenza A virus. Its name derives from the forms of the two kinds of proteins on the surface of its coat, hemagglutinin (H) and neuraminidase (N). H3N2 exchanges genes for internal proteins with other influenza subtypes. H3N2 has tended to dominate in prevalence over H1N1, H1N2, and influenza B. H3N2 strain descended from H2N2 by antigenic shift, in which genes from multiple subtypes re-assorted to form a new virus. Both the H2N2 and H3N2 strains contained genes from avian influenza viruses. |
Reagent Appearance | Sterile Filtered clear solution. |
Type | Rabbit Antibody Polyclonal. |
Immunogen | Recombinant Influenza A/Wisconsin/67/05. |
Storage Procedures | Store at -200C, one month at 40C. |