FOXP3 Polyclonal Antibody

  • 货号:YT5446
  • 应用:WB;IHC;IF;ELISA
  • 种属:Human;Mouse;Rat;Pig
    • 靶点:
    • FOXP3
    • 简介:
    • >>Th17 cell differentiation;>>Inflammatory bowel disease
    • 基因名称:
    • FOXP3
    • 蛋白名称:
    • Forkhead box protein P3
    • Human Swiss Prot No:
    • Q9BZS1
    • Mouse Swiss Prot No:
    • Q99JB6
    • 免疫原:
    • The antiserum was produced against synthesized peptide derived from the C-terminal region of human FOXP3. AA range:381-430
    • 特异性:
    • FOXP3 Polyclonal Antibody detects endogenous levels of FOXP3 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: 1:100-1:300. ELISA: 1:20000.. 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)
    • 其他名称:
    • FOXP3;IPEX;JM2;Forkhead box protein P3;Scurfin
    • 实测条带:
    • 47kD
    • 背景:
    • The protein encoded by this gene is a member of the forkhead/winged-helix family of transcriptional regulators. Defects in this gene are the cause of immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX), also known as X-linked autoimmunity-immunodeficiency syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008],
    • 功能:
    • disease:Defects in FOXP3 are the cause of immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) [MIM:304790]; also known as X-linked autoimmunity-immunodeficiency syndrome. IPEX is characterized by neonatal onset insulin-dependent diabetes mellitus, infections, secretory diarrhea, trombocytopenia, anemia and eczema. It is usually lethal in infancy.,function:Probable transcription factor. Plays a critical role in the control of immune response.,online information:FOXP3 entry,online information:FOXP3 mutation db,similarity:Contains 1 C2H2-type zinc finger.,similarity:Contains 1 fork-head DNA-binding domain.,
    • 细胞定位:
    • Nucleus . Cytoplasm . Predominantly expressed in the cytoplasm in activated conventional T-cells whereas predominantly expressed in the nucleus in regulatory T-cells (Treg). The 41 kDa form derived by proteolytic processing is found exclusively in the chromatin fraction of activated Treg cells (By similarity). .