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AID Polyclonal Antibody
商品货号: PLA019206
适 应 性: 人,小鼠,大鼠
WB IHC IF ELISA
¥600元
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MSDS
说明书
商品描述
  • 基因名称: AICDA
  • 蛋白名称: Activation-induced cytidine deaminase
  • Human_gene_id: 57379
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=57379
  • Human_swiss_prot_no: Q9GZX7
  • Human_swiss_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_swiss_prot_no: Q9WVE0
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/Q9WVE0
  • Rat_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=
  • Rat_swiss_link: http://www.uniprot.org/uniprot/
  • 特异性: AID Polyclonal Antibody detects endogenous levels of AID protein.
  • 组成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 来源: Polyclonal, Rabbit,IgG
  • 稀释: WB 1:500 - 1:2000. IHC-p: 1:100-1:300. ELISA: 1:10000.. IF 1:50-200
  • 纯化工艺: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 浓度: 1 mg/ml
  • 储存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 说明书: 1
  • Msds: MSDS_Antibody.pdf
  • 其他名称: AICDA; AID; Activation-induced cytidine deaminase; Cytidine aminohydrolase
  • 实测条带: 24kD
  • 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.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Nucleus . Cytoplasm . Predominantly cytoplasmic (PubMed:21385873). In the presence of MCM3AP/GANP, relocalizes to the nucleus (By similarity). .
  • 组织表达: Strongly expressed in lymph nodes and tonsils.
  • 科研货号: PLA019206
AID Polyclonal Antibody
Catalog No PLA019206
Product information
  • 基因名称: AICDA
  • 蛋白名称: Activation-induced cytidine deaminase
  • Human_gene_id: 57379
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=57379
  • Human_swiss_prot_no: Q9GZX7
  • Human_swiss_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_swiss_prot_no: Q9WVE0
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/Q9WVE0
  • Rat_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=
  • Rat_swiss_link: http://www.uniprot.org/uniprot/
  • 特异性: AID Polyclonal Antibody detects endogenous levels of AID protein.
  • 组成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 来源: Polyclonal, Rabbit,IgG
  • 稀释: WB 1:500 - 1:2000. IHC-p: 1:100-1:300. ELISA: 1:10000.. IF 1:50-200
  • 纯化工艺: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 浓度: 1 mg/ml
  • 储存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 说明书: 1
  • Msds: MSDS_Antibody.pdf
  • 其他名称: AICDA; AID; Activation-induced cytidine deaminase; Cytidine aminohydrolase
  • 实测条带: 24kD
  • 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.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Nucleus . Cytoplasm . Predominantly cytoplasmic (PubMed:21385873). In the presence of MCM3AP/GANP, relocalizes to the nucleus (By similarity). .
  • 组织表达: Strongly expressed in lymph nodes and tonsils.
  • 科研货号: PLA019206
  • Hunan UPT Biotechnology Co.,Ltd
    Website:www.uptbio.com Servive hotline :4006916686
    E-mail:service@uptbio.com
    Address:
    Room 402, Building 13, Xinggong International Industrial Park, 100 Guyuan Road, Yuelu District, Changsha City, Hunan Province, China.
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