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AICDA (基因名), Single-stranded DNA cytosine deaminase (蛋白名), aicda_human.
产品名称:

Human AICDA/ Single-stranded DNA cytosine deaminase Recombinant Protein
活化诱导胞嘧啶核苷脱氨酶

货号:

R14184h

商标:
EIAab®
监管等级:
别名:

Activation-induced cytidine deaminase, Cytidine aminohydrolase, AID, AID

序列号:
Q9GZX7
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:
Epigenetics
Human AICDA Protein
规格 & 价格: cart
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Human AICDA Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS
在线询价


R&D 技术数据
更多信息,请参阅手册,或联系我们的技术支持: tech@eiaab.com.
基因位点
Cytogenetic band: 12p13.31 by HGNC 12p13.31 by Entrez Gene 12p13.31 by Ensembl
AICDA 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:
Interacts with CTNNBL1; the interaction is important for the immunoglobulin switch activity of AICDA. Interacts (via its NLS) with KPNA1. Interacts with PKA/PRKACA and PRKAR1A/PKR1. Interacts with TRIM28 and NCL (By similarity). Interacts with SUPT6H. Interacts with RNF126.


功能:
Single-stranded DNA-specific cytidine deaminase. Involved in somatic hypermutation (SHM), gene conversion, and class-switch recombination (CSR) in B-lymphocytes by deaminating C to U during transcription of Ig-variable (V) and Ig-switch (S) region DNA. Required for several crucial steps of B-cell terminal differentiation necessary for efficient antibody responses (PubMed:18722174, PubMed:21385873, PubMed:21518874, PubMed:27716525). May also play a role in the epigenetic regulation of gene expression by participating in DNA demethylation (PubMed:21496894).


亚细胞位置:
Nucleus Cytoplasm Predominantly cytoplasmic but shuttles between the nucleus and the cytoplasm.


该产品尚未在任何出版物中被引用。

[1].
"Association between a new polymorphism in the activation-induced cytidine deaminase gene and atopic asthma and the regulation of total serum IgE levels."

[2].
"No association between AICDA 7888 C/T polymorphism, Helicobacter pylori seropositivity, and the risk of atrophic gastritis and gastric cancer in Japanese."

[3].
"Interaction between antibody-diversification enzyme AID and spliceosome-associated factor CTNNBL1."

[4].
"Activation-induced cytidine deaminase shuttles between nucleus and cytoplasm like apolipoprotein B mRNA editing catalytic polypeptide 1."

[5].
"Polymorphisms of IL-4, IL-4R alpha, and AICDA genes in adult allergic asthma."

[6].
"Isolation, tissue distribution, and chromosomal localization of the human activation-induced cytidine deaminase (AID) gene."

[7].
"Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2)."

[8].
"Structural analysis of the activation-induced deoxycytidine deaminase required in immunoglobulin diversification."

[9].
"Activation induced cytidine deaminase mutant (AID-His130Pro) from Hyper IgM 2 patient retained mutagenic activity on SHM artificial substrate."

[10].
"Novel and recurrent AID mutations underlie prevalent autosomal recessive form of HIGM in consanguineous patients."
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