欢迎来到启研生物[ 会员登录 ] [ 立即注册 ]
400-812-0026

购物车0

您购物车为空,赶紧选购吧!
NTAL Polyclonal Antibody
NTAL Polyclonal Antibody
<
>
NTAL Polyclonal Antibody
市场价格
经销商客户: ¥440.0
实验室客户: ¥600.0
近期销售量13 用户评价:comment rank 5()
文件与质量管理
浏览历史 [清空]

商品描述

商品属性

Target:NTAL

Gene Name:LAT2 LAB NTAL WBS15 WBSCR15 WBSCR5 HSPC046

Protein Name: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 1

Human Gene Id:7462

Human Swiss Prot No:Q9GZY6

Mouse Swiss Prot No:Q9JHL0

Rat Swiss Prot No:Q8CGL2

Immunogen:Synthesized peptide derived from human protein . at AA range: 80-160

Specificity:NTAL Polyclonal Antibody detects endogenous levels of protein.

Formulation:Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.

Source:Polyclonal, Rabbit,IgG

Dilution:WB 1:500-2000 ELISA 1:5000-20000

Purification:The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Concentration:1 mg/ml

Storage Stability:-15°C to -25°C/1 year(Do not lower than -25°C)

Observed Band(KD):26kD

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],

Function: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

Subcellular Location:Cell membrane ; Single-pass type III membrane protein . Present in lipid rafts.

Expression: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).

广告说明