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LAB (Phospho-Tyr136) rabbit pAb

说明书

BYab-10490

  • 20UL ¥460 50UL ¥945 100UL ¥1350
  • 货期: 3天左右

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产品简介>

宿主
反应性
应用
WB
分子量(DA)
30kD
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
来源
Polyclonal, Rabbit,IgG
组成(Formulation)
Liquid in PBS containing 50% glycerol, and 0.146% sodium azide.
稀释比例
WB 1:500-2000
纯化工艺(Immunogen)
The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
浓度
1 mg/ml
背景(Background)
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
基因名称(Gene Name)
LAT2 LAB NTAL WBS15 WBSCR15 WBSCR5 HSPC046
蛋白名称
LAB (Phospho-Tyr136)
简称
LAB
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)
Fields
人基因ID
7462
人蛋白质序列数据库
Q9GZY6
小鼠基因ID
56743
小鼠蛋白质序列数据库
Q9JHL0
大鼠基因ID
317676
大鼠蛋白质序列数据库
Q8CGL2
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).
储存(Storage)
-20°C/1 year

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LAB (Phospho-Tyr136) rabbit pAb

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