CD231 Polyclonal Antibody

    • 货号:YT5946
    • 应用:IHC;IF;ELISA
    • 种属:Human;Mouse;Rat
      • 靶点:
      • CD231
      • 简介:
      • >>Transcriptional misregulation in cancer
      • 基因名称:
      • TSPAN7 A15 DXS1692E MXS1 TM4SF2
      • 蛋白名称:
      • Tetraspanin-7 (Tspan-7) (Cell surface glycoprotein A15) (Membrane component chromosome X surface marker 1) (T-cell acute lymphoblastic leukemia-associated antigen 1) (TALLA-1) (Transmembrane 4 superfa
      • Human Gene Id:
      • 7102
      • Human Swiss Prot No:
      • P41732
      • Mouse Swiss Prot No:
      • Q62283
      • 免疫原:
      • Synthetic peptide from human protein at AA range: 101-150
      • 特异性:
      • The antibody detects endogenous CD231
      • 组成:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • 来源:
      • Polyclonal, Rabbit,IgG
      • 稀释:
      • IHC 1:50-200, ELISA 1:10000-20000. 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:
      • Tetraspanin-7 (Tspan-7;Cell surface glycoprotein A15;Membrane component chromosome X surface marker 1;T-cell acute lymphoblastic leukemia-associated antigen 1;TALLA-1;Transmembrane 4 superfamily member 2;CD antigen CD231)
      • 背景:
      • The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is a cell surface glycoprotein and may have a role in the control of neurite outgrowth. It is known to complex with integrins. This gene is associated with X-linked mental retardation and neuropsychiatric diseases such as Huntington's chorea, fragile X syndrome and myotonic dystrophy. [provided by RefSeq, Jul 2008],
      • 功能:
      • disease:Defects in TSPAN7 are the cause of mental retardation X-linked type 58 (MRX58) [MIM:300210]. Mental retardation is characterized by significantly sub-average general intellectual functioning associated with impairments in adaptative behavior and manifested during the developmental period. Non-syndromic mental retardation patients do not manifest other clinical signs.,function:May be involved in cell proliferation and cell motility.,similarity:Belongs to the tetraspanin (TM4SF) family.,tissue specificity:Not solely expressed in T-cells. Expressed in acute myelocytic leukemia cells of some patients.,
      • 细胞定位:
      • Membrane; Multi-pass membrane protein.
      • 组织表达:
      • Not solely expressed in T-cells. Expressed in acute myelocytic leukemia cells of some patients.
      • 产品图片
      • Immunohistochemical analysis of paraffin-embedded human-kidney, antibody was diluted at 1:200