Influenza A [A/Puerto Rico/8/1934 (H1N1)] Hemagglutinin (HA), His-Tag

$378.54 – $2,199.64 excl. VAT

Recombinant Influenza A [A/Puerto Rico/8/1934 (H1N1)] Hemagglutinin (HA) protein, comprising amino acids 1-529, incorporating a C-terminal 6xHis tag, produced in mammalian HEK293 cells.

SDS-PAGE: Reducing SDS-PAGE gel showing purified Influenza H1N1 HA protein, showing protein migrating as a 70-80kDa band.

INFLUENZA A [A/PUERTO RICO/8/1934 (H1N1)] HEMAGGLUTININ (HA), HIS-TAG

This Influenza virus hemagglutinin protein is derived from the HA sequence of the A/Puerto Rico/8/1934 (H1N1) strain (Accession #NP_040980), expressing Asp18-Gn529, and is fused with a 8x Gly-Ser linker and a 6x polyhistidine tag at the C-terminus. The total calculated MW is 59.0kDa. The influenza virus hemagglutinin protein is expressed in HEK293 cells, and DTT-reduced protein migrates as a band of 70-80kDa.

PRODUCT DETAILS – INFLUENZA A [A/PUERTO RICO/8/1934 (H1N1)] HEMAGGLUTININ (HA), HIS-TAG

Recombinant Influenza A Hemagglutinin 1 of the A/Puerto Rico/8/1934 (H1N1) strain.
Includes amino acids 1-529 and a C-terminal His-tag.
Greater than 95% purity by SDS-PAGE.

BACKGROUND

Influenza, commonly known as “the flu”, is an infectious disease of birds and mammals caused by RNA viruses of the family Orthomyxoviridae, the influenza viruses. The virus is divided into three main types (Influenza virus A, Influenza virus B, and Influenza virus C), which are distinguished by differences in two major internal proteins (hemagglutinin (HA) and neuraminidase (NA), which are the most important targets for the immune system. The type A viruses are the most virulent human pathogens among the three influenza types and cause the most severe disease.

Influenza virus hemagglutinin (HA) is a trimer of identical subunits, each of which contains two polypeptides that result from proteolytic cleavage of a single precursor. The two polypeptides are designated HA1 and HA2. The HA2 monomer is a long helical chain, anchored into the membrane, and is “topped” by a “globule” of HA1. Cleavage of the precursor is essential for activation of membrane fusion potential and hence infectivity. For HAs of most subtypes, the site of cleavage is a single arginine residue, and cleavage occurs extracellularly by an as yet unidentified enzyme. The Puerto Rico strain isolated in 1934 is one of the most commonly used laboratory strains, and formed the basis of early influenza vaccines. The structure of HA has been reviewed by Gamblin and Skehel in 2010.