APOBEC3C Antibody Blocking Peptide(bs-12495P)-500ug

APOBEC3C Antibody Blocking Pep

tide(bs-12495P)-500ug
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  • ¥880
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  • bs-12495P
  • 2025年10月16日
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      500ug

    产品编号bs-12495P
    英文名称APOBEC3C Antibody Blocking Peptide
    中文名称载脂蛋白B-mRNA编辑酶复合物3C封闭多肽
    英文别名ABC3C_HUMAN; APOBEC1 like; APOBEC1-like; APOBEC1L; APOBEC3C; Apolipoprotein B mRNA editing enzyme catalytic polypeptide like 3C; ARDC2; ARDC4; ARP5; bK150C2.3; MGC19485; PBI; Phorbolin I; Phorbolin I protein; Probable DNA dC dU editing enzyme APOBEC 3C; Probable DNA dC->dU-editing enzyme APOBEC-3C.
    纯化方法HPLC
    研究领域

    Epigenetics and Nuclear Signaling > Chromatin Modifying Enzymes > Deamination

    Epigenetics and Nuclear Signaling > DNA / RNA > RNA Processing

    Immunology > Immune System Diseases > Antiviral Signaling

    亚基Homodimer. Interacts with human foamy virus protein Bet; this interaction does not induce APOBEC3C degradation, but prevents dimerization and incorporation into virion of the latter. Interacts with TRIB3 and EIF2C2/AGO2.
    亚细胞定位Nucleus. Cytoplasm.
    组织特异性Expressed in spleen, testes, peripherical blood lymphocytes, heart, thymus, prostate and ovary.
    相似性Belongs to the cytidine and deoxycytidylate deaminase family.
    功能Host cellular restriction factor that may have antiviral activities against exogenous and endogenous viruses, as well as retrotransposons. May also play a role in the epigenetic regulation of gene expression through the process of active DNA demethylation.
    保存条件Shipped at 4℃. Stored at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    注意事项This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    背景资料APOBEC proteins inhibit retroviruses by deaminating cytosine residues of viral RNA and DNA. The seven APOBEC3 genes or pseudogenes are found in a cluster thought to result from gene duplication on chromosome 22. Like APOBEC3G, APOBEC3F deaminates deoxycytosine to deoxyuracil in the minus strand of HIV-1 DNA, resulting in G to A hypermutation in the plus strand of DNA. Thus, APOBEC3G and APOBEC3F provide a mechanism for innate immunity to retroviruses, and are also likely contribute to sequence variation observed in many viruses. Viral infectivity factor (Vif) imparts APOBEC3G and APOBEC3F resistance to HIV through impaired translation of their mRNA and accelerated posttranslational degradation of the APOBEC3 proteins by the 26S proteasome. Interestingly, HIV-1 Vif cannot form a complex with APOBEC3G or APOBEC3F of mouse origin as it does with the human protein, and thus mouse APOBEC3G and APOBEC3F function as a potent inhibitors of wildtype HIV-1 replication, where human APOBEC3G and APOBEC3F are only able to inhibit Vif-deficient HIV-1 replication. This implies that induction of APOBEC3G and APOBEC3F activity or a method of blocking their interaction with Vif may provide a method for therapeutic intervention.

     

     

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