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首页  >  重组蛋白  >  Human APOBEC3D Recombinant Protein
APOBEC3D (基因名), DNA dC->dU-editing enzyme APOBEC-3D (蛋白名), ABC3D_HUMAN.
产品名称:

Human APOBEC3D/ DNA dC->dU-editing enzyme APOBEC-3D Recombinant Protein

货号:
-
商标:
EIAab®
监管等级:
别名:

A3D

序列号:
Q96AK3
来源:
E.coli
种属:
Human
标签:
His
纯度:
>90% by SDS-PAGE
浓度:
Reconstitution Dependent
形态:
Liquid
内毒素水平:
Please contact protein@eiaab.com The technician for more information.
应用:
存储缓冲液:
50mM NaH2PO4, 500mM NaCl Buffer with 500mM Imidazole, 10%glycerol(PH8.0)
存储:
Store at -20°C. (Avoid repeated freezing and thawing.)
研究领域:
-
Human APOBEC3D Protein
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Human APOBEC3D Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS


基因位点
Cytogenetic band: 22q13.1 by HGNC 22q13.1 by Entrez Gene 22q13.1 by Ensembl
APOBEC3D Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
基因位点
通用注释


亚单元:
N/A


功能:
DNA deaminase (cytidine deaminase) which acts as an inhibitor of retrovirus replication and retrotransposon mobility via deaminase-dependent and -independent mechanisms. Exhibits antiviral activity against vif-deficient HIV-1. After the penetration of retroviral nucleocapsids into target cells of infection and the initiation of reverse transcription, it can induce the conversion of cytosine to uracil in the minus-sense single-strand viral DNA, leading to G-to-A hypermutations in the subsequent plus-strand viral DNA. The resultant detrimental levels of mutations in the proviral genome, along with a deamination-independent mechanism that works prior to the proviral integration, together exert efficient antiretroviral effects in infected target cells. Selectively targets single-stranded DNA and does not deaminate double-stranded DNA or single-or double-stranded RNA. May inhibit the mobility of LTR and non-LTR retrotransposons.


亚细胞位置:
Cytoplasm Cytoplasm P-body


该产品尚未在任何出版物中被引用。

[1].
"An anthropoid-specific locus of orphan C to U RNA-editing enzymes on chromosome 22."

[2].
"APOBEC3G restricts HIV-1 to a greater extent than APOBEC3F and APOBEC3DE in human primary CD4+ T cells and macrophages."

[3].
"Endogenous origins of HIV-1 G-to-A hypermutation and restriction in the nonpermissive T cell line CEM2n."

[4].
"Retroelements versus APOBEC3 family members: No great escape from the magnificent seven."

[5].
"HIV-1 replication and APOBEC3 antiviral activity are not regulated by P bodies."

[6].
"Human and rhesus APOBEC3D, APOBEC3F, APOBEC3G, and APOBEC3H demonstrate a conserved capacity to restrict Vif-deficient HIV-1."

[7].
"APOBEC3 proteins mediate the clearance of foreign DNA from human cells."

[8].
"The APOBEC3 cytidine deaminases: an innate defensive network opposing exogenous retroviruses and endogenous retroelements."

[9].
"Messenger RNA editing in mammals: new members of the APOBEC family seeking roles in the family business."

[10].
"Species-specific exclusion of APOBEC3G from HIV-1 virions by Vif."
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