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AB49013

Recombinant Hepatitis B Virus Core Antigen protein (Tag Free)

Recombinant Hepatitis B Virus Core Antigen protein (Tag Free)

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(3 Publications)

Recombinant Hepatitis B Virus Core Antigen protein (Tag Free) 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.

別名を表示する

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

Key facts

精製度

>95% SDS-PAGE

Purification method is proprietary.

発現系

Escherichia coli

タグ

Tag free

アプリケーション

FuncS, WB, ELISA, SDS-PAGE

applications

生物活性

Yes

生物学的活性

Reacts strongly with human HBV positive serum.

アクセッション番号

P03147

アニマルフリー

No

キャリアフリー

No

種

Hepatitis B virus subtype adyw

バッファー組成

pH: 7.2 - 7.6 Constituents: PBS, 50% Glycerol (glycerin, glycerine), 0.435% Sodium chloride

storage-buffer

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Reactivity", "Dilution Info", "Notes"] }, "values": { "SDS-PAGE": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" }, "ELISA": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" }, "WB": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" }, "FuncS": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" } } }

製品の詳細

Reacts strongly with human HBV positive serum.

配列情報

[{"linker":null,"sequence":"MDIDPYKEFGATVELLSFLPSDFFPSVRDLLDNASALYREALESPEHCSPHHTALRQAILCWGELMTLATWVGGNLEDPISRDLVVSYVNTNMGLKFRQLLWFHISCLTFGRETVIEYLVSFGVWIRTPPAYRPPNAPILSTLPETTVVRRRGRSPRRRTPSPRRRRSQSPRRRRSQSRESQC","proteinLength":"Full Length","predictedMolecularWeight":"18 kDa","actualMolecularWeight":null,"aminoAcidEnd":183,"aminoAcidStart":1,"nature":"Recombinant","expressionSystem":"Escherichia coli","accessionNumber":"P03147","tags":[]}]

出荷温度及び保存条件

製品の状態
Liquid
出荷温度
Blue Ice
短期保存期間
1-2 weeks
短期保存温度
+4°C
長期保存温度
-20°C
分注に関する情報
Upon delivery aliquot
保管に関する情報
Avoid freeze / thaw cycle
True

補足情報

This supplementary information is collated from multiple sources and compiled automatically.

The Hepatitis B Virus Core Antigen also known as HBV core antigen or Hep B core is an important component of the hepatitis B virus (HBV). This antigen often referred to simply as 'core' forms the nucleocapsid of the virus. The HBV core antigen consists of a protein structure with a mass of approximately 21 kilodaltons. It is primarily expressed within the hepatocytes the liver cells where it plays a pivotal role in viral replication and assembly. The HBV core antigen is also referred to in studies as HBV protein or B core.
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.

The hepatitis B core antigen is strongly linked to chronic hepatitis B infection and liver diseases such as cirrhosis and hepatocellular carcinoma. The persistence of the core antigen in infected hepatocytes signifies ongoing viral replication which can lead to liver inflammation and damage. The interaction of the core antigen with immune system components such as anti-HBc antibodies assists in the diagnosis and monitoring of disease progression. It connects to the envelope proteins during the disease process which are important in immune system evasion and chronic infection establishment.

一般的な情報

機能

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.

配列の類似性

Belongs to the orthohepadnavirus core antigen family.

翻訳後修飾

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.

製品プロトコール

ターゲットの情報

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.
See full target information C

追加のターゲット

Hepatitis B Virus Core Antigen,C,C,,

文献 (3)

Recent publications for all applications. Explore the full list and refine your search

Cell reports 38:110284 PubMed35081341

2022

Macrophages activated by hepatitis B virus have distinct metabolic profiles and suppress the virus via IL-1β to downregulate PPARα and FOXO3.

Applications

Unspecified application

Species

Unspecified reactive species

Yumei Li,Yanwen Zhu,Shu Feng,Yuji Ishida,Tsu-Pei Chiu,Takeshi Saito,Sean Wang,David K Ann,Jing-Hsiung James Ou

Virus research 271:197677 PubMed31376401

2019

Pyrimidotriazine derivatives as selective inhibitors of HBV capsid assembly.

Applications

Unspecified application

Species

Unspecified reactive species

Masaaki Toyama,Norikazu Sakakibara,Midori Takeda,Mika Okamoto,Koichi Watashi,Takaji Wakita,Masaya Sugiyama,Masashi Mizokami,Masanori Ikeda,Masanori Baba

Biotechnology progress 34:130-140 PubMed28884522

2017

Development of a high-throughput microscale cell disruption platform for Pichia pastoris in rapid bioprocess design.

Applications

Unspecified application

Species

Unspecified reactive species

Benjamin A F Bláha,Stephen A Morris,Olotu W Ogonah,Sophie Maucourant,Vincenzo Crescente,William Rosenberg,Tarit K Mukhopadhyay
View all publications

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