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AID Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PT5566
产品名称
AID Rabbit Polyclonal Antibody
别名
AICDA; AID; Activation-induced cytidine deaminase; Cytidine aminohydrolase
类别
常规抗体
基因名称
AICDA
蛋白名称
Activation-induced cytidine deaminase
推荐应用
WB
反应种属
Human,Mouse,Rat
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.
Human Gene ID
57379
Human Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=57379
Human Swissprot No.
Q9GZX7
Human Swissprot Link
http://www.uniprot.org/uniprotkb/Q9GZX7/entry
Mouse Gene ID
11628
Mouse Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=11628
Mouse Swissprot No.
Q9WVE0
Mouse Swissprot Link
http://www.uniprot.org/uniprot/Q9WVE0
Rat Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=
Rat Swissprot Link
http://www.uniprot.org/uniprot/
免疫原
The antiserum was produced against synthesized peptide derived from the Internal region of human AICDA. AA range:81-130
特异性
AID Polyclonal Antibody detects endogenous levels of AID protein.
稀释度
WB 1:500 - 1:2000. IHC-p: 1:100-1:300. ELISA: 1:10000.. IF 1:50-200
预测分子量
24kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
This gene encodes a RNA-editing deaminase that is a member of the cytidine deaminase family. The protein is involved in somatic hypermutation, gene conversion, and class-switch recombination of immunoglobulin genes. Defects in this gene are the cause of autosomal recessive hyper-IgM immunodeficiency syndrome type 2 (HIGM2). [provided by RefSeq, Feb 2009],
组织表达
Strongly expressed in lymph nodes and tonsils.
细胞定位
Nucleus . Cytoplasm . Predominantly cytoplasmic (PubMed:21385873). In the presence of MCM3AP/GANP, relocalizes to the nucleus (By similarity). .
信号通路
Intestinal immune network for IgA production;Primary immunodeficiency;
功能
catalytic activity:Cytidine + H(2)O = uridine + NH(3).,cofactor:Zinc.,disease:Defects in AICDA are the cause of autosomal recessive hyper-IgM immunodeficiency syndrome type 2 (HIGM2) [MIM:605258]. HIGM2 is characterized by normal or elevated serum IgM levels with absence of IgG, IgA, and IgE, resulting in a profound susceptibility to bacterial infections. HIGM2 causes the absence of Ig class switch recombination (CSR), the lack of Ig somatic hypermutations, and lymph node hyperplasia caused by the presence of giant germinal centers.,function:RNA-editing deaminase involved in somatic hypermutation, gene conversion, and class-switch recombination. Required for several crucial steps of B-cell terminal differentiation necessary for efficient antibody responses.,online information:AICDA mutation db,similarity:Belongs to the cytidine and deoxycytidylate deaminase family.,tissue specificity:Strongly expressed in lymph nodes and tonsils.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Western Blot analysis of Hela, HepG2 cells using AID Polyclonal Antibody.. Secondary antibody was diluted at 1:20000

Immunohistochemical analysis of paraffin-embedded human-colon-cancer, antibody was diluted at 1:100

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