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Recombinant Mouse DNA dC->dU-editing enzyme APOBEC-3 (Apobec3)

  • 中文名稱:
    Recombinant Mouse DNA dC->dU-editing enzyme APOBEC-3(Apobec3)
  • 貨號:
    CSB-YP859956MO
  • 說明書:
  • 規格:
  • 來源:
    Yeast
  • 其他:
  • 中文名稱:
    Recombinant Mouse DNA dC->dU-editing enzyme APOBEC-3(Apobec3)
  • 貨號:
    CSB-EP859956MO
  • 說明書:
  • 規格:
  • 來源:
    E.coli
  • 其他:
  • 中文名稱:
    Recombinant Mouse DNA dC->dU-editing enzyme APOBEC-3(Apobec3)
  • 貨號:
    CSB-EP859956MO-B
  • 說明書:
  • 規格:
  • 來源:
    E.coli
  • 共軛:
    Avi-tag Biotinylated

    E. coli biotin ligase (BirA) is highly specific in covalently attaching biotin to the 15 amino acid AviTag peptide. This recombinant protein was biotinylated in vivo by AviTag-BirA technology, which method is BriA catalyzes amide linkage between the biotin and the specific lysine of the AviTag.

  • 其他:
  • 中文名稱:
    Recombinant Mouse DNA dC->dU-editing enzyme APOBEC-3(Apobec3)
  • 貨號:
    CSB-BP859956MO
  • 說明書:
  • 規格:
  • 來源:
    Baculovirus
  • 其他:
  • 中文名稱:
    Recombinant Mouse DNA dC->dU-editing enzyme APOBEC-3(Apobec3)
  • 貨號:
    CSB-MP859956MO
  • 說明書:
  • 規格:
  • 來源:
    Mammalian cell
  • 其他:

產品詳情

  • 純度:
    >85% (SDS-PAGE)
  • 基因名:
    Apobec3
  • Uniprot No.:
  • 別名:
    Apobec3DNA dC->dU-editing enzyme APOBEC-3; EC 3.5.4.38; Apolipoprotein B mRNA-editing complex 3; Arp3; CEM-15; CEM15
  • 種屬:
    Mus musculus (Mouse)
  • 蛋白長度:
    full length protein
  • 表達區域:
    1-429
  • 氨基酸序列
    MGPFCLGCSH RKCYSPIRNL ISQETFKFHF KNLGYAKGRK DTFLCYEVTR KDCDSPVSLH HGVFKNKDNI HAEICFLYWF HDKVLKVLSP REEFKITWYM SWSPCFECAE QIVRFLATHH NLSLDIFSSR LYNVQDPETQ QNLCRLVQEG AQVAAMDLYE FKKCWKKFVD NGGRRFRPWK RLLTNFRYQD SKLQEILRPC YIPVPSSSSS TLSNICLTKG LPETRFCVEG RRMDPLSEEE FYSQFYNQRV KHLCYYHRMK PYLCYQLEQF NGQAPLKGCL LSEKGKQHAE ILFLDKIRSM ELSQVTITCY LTWSPCPNCA WQLAAFKRDR PDLILHIYTS RLYFHWKRPF QKGLCSLWQS GILVDVMDLP QFTDCWTNFV NPKRPFWPWK GLEIISRRTQ RRLRRIKESW GLQDLVNDFG NLQLGPPMS
  • 蛋白標簽:
    Tag?type?will?be?determined?during?the?manufacturing?process.
    The tag type will be determined during production process. If you have specified tag type, please tell us and we will develop the specified tag preferentially.
  • 產品提供形式:
    Lyophilized powder
    Note: We will preferentially ship the format that we have in stock, however, if you have any special requirement for the format, please remark your requirement when placing the order, we will prepare according to your demand.
  • 復溶:
    We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Please reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL.We recommend to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20℃/-80℃. Our default final concentration of glycerol is 50%. Customers could use it as reference.
  • 儲存條件:
    Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.
  • 保質期:
    The shelf life is related to many factors, storage state, buffer ingredients, storage temperature and the stability of the protein itself.
    Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C.
  • 貨期:
    Delivery time may differ from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
    Note: All of our proteins are default shipped with normal blue ice packs, if you request to ship with dry ice, please communicate with us in advance and extra fees will be charged.
  • 注意事項:
    Repeated freezing and thawing is not recommended. Store working aliquots at 4°C for up to one week.
  • Datasheet :
    Please contact us to get it.

產品評價

靶點詳情

  • 功能:
    DNA deaminase (cytidine deaminase) which acts as an inhibitor of retrovirus replication and retrotransposon mobility via deaminase-dependent and -independent mechanisms. Selectively targets single-stranded DNA and does not deaminate double-stranded DNA or single- or double-stranded RNA. Exhibits antiviral activity against HIV-1, simian immunodeficiency viruses (SIVs), mouse mammary tumor virus (MMTV) and friend murine leukemia virus (FrMLV) and may inhibit the mobility of LTR retrotransposons.
  • 基因功能參考文獻:
    1. The distribution of AID and A3s in the epithelial cells as well as germinal centres. PMID: 29343743
    2. By developing transgenic mice with mutations in the cytidine deamination domains needed for enzymatic activity and interaction with viral RNA, the authors show that APOBEC3 proteins can still restrict in vivo infection by interacting with reverse transcriptase and blocking its activity. PMID: 29593034
    3. our current work indicated that APOBEC3 copy number variations might have a good screening accuracy for breast cancer. PMID: 27602762
    4. APOBEC3 can restrict retroviruses in a type I interferon-independent manner in vivo. By contrast, the ability of APOBEC3 to promote neutralizing antibody responses is type I interferon-dependent. PMID: 28415995
    5. These results indicate that the mechanisms of APOBEC3 restriction of Koala Retrovirus by humanA3G and mouseA3 differ (deamination dependent vs. independent) and glyco-gag does not play a role in the restriction. PMID: 26253512
    6. The Apobec3/Rfv3-dependent neutralizing antibody response correlated with Friend virus-specific IgG2 titers and that the in vivo neutralization potency of Apobec3/Rfv3-resistant antisera was dependent on activating Fcgamma receptors. PMID: 25589647
    7. A3 shifts the balance, from the fast antibody response mediated by marginal zone B cells with little affinity maturation, to a more sustained germinal center B-cell response PMID: 25501566
    8. Authors find that the number of N-glycosylated residues in glycosylated Pr80 inversely correlates with the sensitivity of a gammaretrovirus to deamination by mouse APOBEC3. PMID: 25505062
    9. APOBEC3A and APOBEC3B are more abundant on protein level in chronic lymphocytic leukemia (CLL) than in AID, and clustered genomic C>T mutations outside the Ig locus occur at APOBEC3 hot spot motifs in IgV-Mut CLL. PMID: 24840555
    10. APOBEC3 acts as a key player in generating virus-specific neutralizing antibodies that could be harnessed for vaccine development. PMID: 24821801
    11. loss genotypes of APOBEC3 deletion predispose their carriers to epithelial ovarian cancer (EOC). PMID: 24577894
    12. The mA3 (APOBEC3) exon 5 is indeed a functional element that influences protein synthesis at a post-transcriptional level. PMID: 22275865
    13. Despite the fact that APOBEC3 in murine leukemia viruse particles does not induce detectable deaminations upon infection, its deaminase activity is easily detected in virus lysates. PMID: 24453360
    14. APOBEC3G inhibits DND1 function to regulate microRNA activity. PMID: 23890083
    15. HIV replication persists despite the inability of HIV to develop resistance to APOBEC3 in the absence of Vif. PMID: 23555255
    16. APOBEC3 restricted mouse mammary tumor virus through inhibition of early reverse transcription. PMID: 23449789
    17. IFN-alpha can act primarily through Apobec3 to inhibit acute infection of pathogenic Friend retrovirus in vivo. PMID: 23315078
    18. IFN-alpha and LPS induce Apobec3 via different pathways that can be manipulated to enhance the intracellular store of A3 and potentially enhance A3 antiviral function in the host. PMID: 22972924
    19. Loss of APOBEC3 gene facilitates efficient sexual transmission of murine leukemia virus. PMID: 22691411
    20. restriction of murine leukemia viruses by mouse APOBEC3 PMID: 22666481
    21. Apobec3 promotes the release of substantial levels of noninfectious virions in the plasma during acute Friend virus infection. PMID: 21998583
    22. novel mechanism in which APOBEC3G promotes colorectal cancer hepatic metastasis through inhibition of miR-29-mediated suppression of MMP2 PMID: 21985787
    23. Phosphorylation directly regulates the intrinsic DNA cytidine deaminase activity of activation-induced deaminase and APOBEC3G protein PMID: 21659520
    24. These data point to a role for APOBEC3 proteins in limiting infectivity of milk-transmitted viruses. PMID: 21147467
    25. This review discusses recent advances the understanding of the dynamic interplay of Vif with the antiviral APOBEC3 enzymes. PMID: 20538015
    26. The preponderance of evidence strongly indicates that Rfv3 is encoded by Apobec3, and while BAFF-R defects may exacerbate viremia in A/WySn mice, it is not Rfv3. PMID: 20980520
    27. report a murine leukemia virus (MuLV) that utilizes its glycosylated Gag protein (gGag) to evade APOBEC3 PMID: 20702647
    28. Data suggest that Apobec3 indirectly influences FV-specific neutralizing Ab responses by reducing virus-induced immune dysfunction. PMID: 20566830
    29. analysis of how small molecular compounds inhibit HIV-1 replication through specifically stabilizing APOBEC3G PMID: 20363737
    30. establishment of XMRV infection in patients may be dependent on infection of A3G/A3F-deficient cells, and cells expressing low levels of A3G/A3F, such as prostate cancer cells, may be ideal producers of infectious XMRV PMID: 20335265
    31. APOBEC3G markedly inhibits retrotransposition of IAP and MusD elements, and induces G-to-A hypermutations in their DNA copies PMID: 15674295
    32. both APOBEC2 (despite being an ancestral member of the family with no obvious redundancy in muscle) and APOBEC3 (despite its proposed role in restricting endogenous retrotransposition) are inessential for mouse development, survival, or fertility PMID: 16055735
    33. separation of function of the cytidine deaminase domains is maintained in hA3B and hA3F, but roles of the two domains are reversed in mouse A3 PMID: 17020885
    34. data indicate that APOBEC3G is not a restriction factor for vaccinia virus replication nor is vaccinia virus able to degrade APOBEC3G PMID: 17052331
    35. mouse A3-containing and human A3G-containing virions showed a marked decrease in titre; A3(-/-) mice were more susceptible to MMTV infection, because virus spread was more rapid and extensive than in their wild-type littermates PMID: 17259974
    36. These results for the first time suggest mA3 editing immediately preceding the integration event that led to retroviral endogenization, contributing to inactivation of infectivity. PMID: 17967065
    37. Study compared the antiviral activities of human and murine Apobec3 (A3), and found that, HIV is able to resist human A3G but is sensitive to murine A3, whereas murine leukemia virus is relatively resistant to murine A3 but sensitive to human A3G. PMID: 18032489
    38. APOBEC3 is not an essential mediator of the IFN-mediated inhibition of hepatitis B virus in vivo. PMID: 18434399
    39. The interaction of DND1 and APOBEC3 could be one mechanism for maintaining viability of germ cells and for preventing germ cell tumor development PMID: 18509452
    40. The inefficient incorporation of endogenous APOBEC3 (mA3) appears to be a strategy by which MLV escapes the inhibitory effect of mA3. PMID: 18572219
    41. IAPE and HERV-K elements are restricted at the entry, amplification and integration into their target genomes by the host APOBEC3 proteins. PMID: 18702815
    42. study demonstrates that Rfv3 is encoded by Apobec3; Apobec3 maps to the same chromosome region as Rfv3 and has broad inhibitory activity against retroviruses, including HIV PMID: 18772436
    43. upon infection with the pathogenic Friend virus complex, (BALB/c x C57BL/6)F(1) mice displayed an exacerbated erythroid cell proliferation when the mice carried a targeted disruption of the C57BL/6-derived APOBEC3 allele. PMID: 18786991
    44. APOBEC3G restricts replication and pathogenesis of M-MuLV in vivo PMID: 19150103
    45. Increasing the levels of this intrinsic antiretroviral factor in vivo can lead to increased levels of restriction because of higher levels of both cell-intrinsic as well as virion-packaged APOBEC3. PMID: 19153238

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  • 亞細胞定位:
    Cytoplasm.
  • 蛋白家族:
    Cytidine and deoxycytidylate deaminase family
  • 組織特異性:
    Expressed in spleen, node and lung.
  • 數據庫鏈接:


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