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Hepatitis A Virus VP1 Recombinant ( HAV VP1 )

DescriptionThe E.Coli derived 48 kDa recombinant protein contains the VP1 immunodominant regions, amino acids 502-605.Purification MethodHAV VP1 protein was purified by proprietary chromatographic technique.PurityHAV VP1 protein is >90% pure as

$303.00

Data sheet

Storage HAV VP1 protein although stable at 4°C for 1 week, should be stored below -18°C. Please prevent freeze thaw cycles.
Formulation 10mM CBB, pH9.6, 0.1% SDS and 50% glycerol.
Purity HAV VP1 protein is >90% pure as determined by 10% PAGE (coomassie staining).
Applications HAV VP1 antigen is suitable for ELISA and Western blots, excellent antigen for detection of HAV with minimal specificity problems.
Description The E.Coli derived 48 kDa recombinant protein contains the VP1 immunodominant regions, amino acids 502-605.
Protein Background Forty-two antigenic domains were identified across the hepatitis A virus (HAV) polyprotein by using a set of 237 overlapping 20-mer synthetic peptides spanning the entire HAV polyprotein. Nineteen antigenic domains were found within the structural proteins, and 22 were found within the nonstructural proteins, with 1 domain spanning the junction of VP1 and P2A proteins. Five of these domains were considered immunodominant, as judged by both the breadth and the strength of their immunoreactivity. One domain is located within the VP2 protein at position 57-90 aa. A second domain, located at position 767-842 aa, contains the C-terminal part of the VP1 protein and the entire P2A protein. A third domain, located at position 1403-1456 aa, comprises the C-terminal part of the P2C protein and the N-terminal half of the P3A protein. The fourth domain, located at position 1500-1519 aa, includes almost the entire P3B, and the last domain, located at position 1719-1764 aa, contains the C-terminal region of the P3C protein and the N-terminal region of the P3D protein. Four of the five most immunoreactive domains are derived from small HAV proteins and/or encompass protein cleavage sites separating different HAV proteins.
Expression host Escherichia Coli.
Purification Method HAV VP1 protein was purified by proprietary chromatographic technique.
Storage buffer Km=740uM, Kcat = 30s-1, Kcat/Km=4.1mM-1s-1 with peptide substrate ATLNFPISPW.
Virus Test 20mM HEPES, pH7.0 and 10% Glycerol.

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