Description
Application: WB, IF, IP, ELISA, ICC
Clonality: Monoclonal
Host: Mouse
Purification: IgG
Reactivity: Influenza B Virus
Hemagglutinin (HA) binds to sialic acid-containing receptors on the cell surface, bringing about the attachment of the virus particle to the cell. Plays a major role in the determination of host range restriction and virulence. ClassIviral fusion protein. Responsible for penetration of the virus into the cell cytoplasm by mediating
the fusion of the membrane of the endocytosed virus particle with the endosomal membrane. Low pH in endosomes induce an irreversible conformationalchange in HA2, releasing the fusion hydrophobic peptide. Several trimers are required to form a
competent fusion pore. Application: 1) Western blotting (1/500~1/1,000 dilution)
2) Immunofluorescent and Immunocytochemical staining (1/100~1/200 dilution)
3) Immunoprecipitation (1/200 dilution)
4) ELISA (assay dependent)
Specificity]
According to Ref.1 during epidemic in Osaka 1996-97, 1H12 antibody reacted with HA protein of most of Influenza B virus isolates belonging to Victoria group tested (70/73 strains) and none of clinical 27 isolates belonging to Yamagata group as examined by PAP staining. However later test with IF staining it also reacts with some of Yamagata group strains like B/Florida/4/2006. However, note that HA changes during passages and may change reactivity to this antibody.
No cross reactivity with any strains of influenza A viruse.
View AllClose
Clonality: Monoclonal
Host: Mouse
Purification: IgG
Reactivity: Influenza B Virus
Hemagglutinin (HA) binds to sialic acid-containing receptors on the cell surface, bringing about the attachment of the virus particle to the cell. Plays a major role in the determination of host range restriction and virulence. ClassIviral fusion protein. Responsible for penetration of the virus into the cell cytoplasm by mediating
the fusion of the membrane of the endocytosed virus particle with the endosomal membrane. Low pH in endosomes induce an irreversible conformationalchange in HA2, releasing the fusion hydrophobic peptide. Several trimers are required to form a
competent fusion pore. Application: 1) Western blotting (1/500~1/1,000 dilution)
2) Immunofluorescent and Immunocytochemical staining (1/100~1/200 dilution)
3) Immunoprecipitation (1/200 dilution)
4) ELISA (assay dependent)
Specificity]
According to Ref.1 during epidemic in Osaka 1996-97, 1H12 antibody reacted with HA protein of most of Influenza B virus isolates belonging to Victoria group tested (70/73 strains) and none of clinical 27 isolates belonging to Yamagata group as examined by PAP staining. However later test with IF staining it also reacts with some of Yamagata group strains like B/Florida/4/2006. However, note that HA changes during passages and may change reactivity to this antibody.
No cross reactivity with any strains of influenza A viruse.