LAB (Phospho Tyr136) rabbit pAb

    • 货号:YP1719
    • 应用:WB
    • 种属:Human;Mouse;Rat
      • 靶点:
      • LAB
      • 基因名称:
      • LAT2 LAB NTAL WBS15 WBSCR15 WBSCR5 HSPC046
      • 蛋白名称:
      • LAB (Phospho-Tyr136)
      • Human Gene Id:
      • 7462
      • Human Swiss Prot No:
      • Q9GZY6
      • Mouse Swiss Prot No:
      • Q9JHL0
      • 免疫原:
      • Synthesized peptide derived from human LAB (Phospho-Tyr136)
      • 特异性:
      • This antibody detects endogenous levels of LAB (Phospho-Tyr136) at Human, Mouse,Rat
      • 组成:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • 来源:
      • Polyclonal, Rabbit,IgG
      • 稀释:
      • WB 1:500-2000
      • 纯化工艺:
      • The antibody was affinity-purified from rabbit serum by affinity-chromatography using 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:
      • Linker for activation of T-cells family member 2 (Linker for activation of B-cells) (Membrane-associated adapter molecule) (Non-T-cell activation linker) (Williams-Beuren syndrome chromosomal region 15 protein) (Williams-Beuren syndrome chromosomal region 5 protein)
      • 实测条带:
      • 30kD
      • 背景:
      • This gene is one of the contiguous genes at 7q11.23 commonly deleted in Williams syndrome, a multisystem developmental disorder. This gene consists of at least 14 exons, and its alternative splicing generates 3 transcript variants, all encoding the same protein. [provided by RefSeq, Jul 2008],
      • 功能:
      • disease:Defects in LAT2 may be a cause of certain cardiovascular and musculo-skeletal abnormalities observed in Williams-Beuren syndrome (WBS) [MIM:194050]. WBS is a rare developmental disorder. It is a contiguous gene deletion syndrome involving genes from chromosome band 7q11.23.,function:Involved in FCER1 (high affinity immunoglobulin epsilon receptor)-mediated signaling in mast cells. May also be involved in BCR (B-cell antigen receptor)-mediated signaling in B-cells and FCGR1 (high affinity immunoglobulin gamma Fc receptor I)-mediated signaling in myeloid cells. Couples activation of these receptors and their associated kinases with distal intracellular events through the recruitment of GRB2.,PTM:May be polyubiquitinated.,PTM:Phosphorylated on tyrosines following cross-linking of BCR in B-cells, FCGR1 in myeloid cells, or FCER1 in mast cells; which induces the recruitment of GRB2.,s
      • 细胞定位:
      • Cell membrane ; Single-pass type III membrane protein . Present in lipid rafts.
      • 组织表达:
      • Highly expressed in spleen, peripheral blood lymphocytes, and germinal centers of lymph nodes. Also expressed in placenta, lung, pancreas and small intestine. Present in B-cells, NK cells and monocytes. Absent from T-cells (at protein level).
      • 产品图片
      • Western Blot analysis of 1 HepG2 cell, 2 Serum-free treated ,using primary antibody at 1:1000 dilution. Secondary antibody(catalog#:RS23920) was diluted at 1:10000