Recombinant Hepatitis B Virus Core Antigen protein
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(3 Publications)
Recombinant Hepatitis B Virus Core Antigen protein is a Hepatitis B virus subtype adyw Full Length protein, in the 1 to 183 aa range, expressed in Escherichia coli, with >95%, suitable for SDS-PAGE, ELISA, WB, FuncS.
View Alternative Names
Capsid protein, Core antigen, Core protein, HBcAg, p21.5, C, Capsid protein, Core antigen, Core protein, HBcAg, p21.5, C, Capsid Protein, Core and e antigen, Core antigen, Core protein, HBVgp4, HBc, HBcAg, Hepatitis B Virus core antigen, Hepatitis B core antigen, p21.5, precore/core protein, Capsid protein, Core antigen, Core protein, HBcAg, p21.5, C, External core antigen, HBeAg, Precore protein, p25, C, Capsid protein, Core antigen, Core protein, HBcAg, p21.5, C
Reactivity data
Product details
Sequence info
Properties and storage information
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The hepatitis B core antigen is integral for the assembly of the viral capsid which protects the viral genome during infection. It functions as part of a larger complex with other viral proteins including the pre-core and envelope proteins to facilitate viral lifecycle processes. This antigen allows for the encapsidation of viral RNA and serves as a scaffold for reverse transcription of the viral genome ensuring replication fidelity and successful infection spread.
Pathways
The hepatitis B core antigen is essential in the viral replication pathway and the HBV lifecycle pathway. It interacts closely with HBV polymerase during the packaging of viral genome into the capsid. These interactions are important for the transformation of RNA into DNA a critical step in viral maturation. The antigen is related to the HBx protein through these pathways; the HBx protein modulates viral replication and can influence the pathogenesis of the virus.
Specifications
Form
Liquid
Additional notes
Purification method is proprietary.
General info
Function
Self assembles to form an icosahedral capsid. Most capsids appear to be large particles with an icosahedral symmetry of T=4 and consist of 240 copies of capsid protein, though a fraction forms smaller T=3 particles consisting of 180 capsid proteins. Entering capsids are transported along microtubules to the nucleus. Phosphorylation of the capsid is thought to induce exposure of nuclear localization signal in the C-terminal portion of the capsid protein that allows binding to the nuclear pore complex via the importin (karyopherin-) alpha and beta. Capsids are imported in intact form through the nuclear pore into the nuclear basket, where it probably binds NUP153. Only capsids that contain the mature viral genome can release the viral DNA and capsid protein into the nucleoplasm. Immature capsids get stuck in the basket. Capsids encapsulate the pre-genomic RNA and the P protein. Pre-genomic RNA is reverse-transcribed into DNA while the capsid is still in the cytoplasm. The capsid can then either be directed to the nucleus, providing more genomes for transcription, or bud through the endoplasmic reticulum to provide new virions.
Sequence similarities
Belongs to the orthohepadnavirus core antigen family.
Post-translational modifications
Phosphorylated by host SRPK1, SRPK2, and maybe protein kinase C or GAPDH. Phosphorylation is critical for pregenomic RNA packaging. Protein kinase C phosphorylation is stimulated by HBx protein and may play a role in transport of the viral genome to the nucleus at the late step during the viral replication cycle.
Target data
Additional targets
Publications (3)
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Cell reports 38:110284 PubMed35081341
2022
Applications
Unspecified application
Species
Unspecified reactive species
Virus research 271:197677 PubMed31376401
2019
Applications
Unspecified application
Species
Unspecified reactive species
Biotechnology progress 34:130-140 PubMed28884522
2017
Applications
Unspecified application
Species
Unspecified reactive species
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