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LAB (Phospho-Tyr136) rabbit pAb

Refer to | for labeled antibodies

Specification

BYab-10490

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Host
Reactiveness
Use
Molecular weight (DA)
30kD
Immunogen
Synthesized peptide derived from human LAB (Phospho-Tyr136)
Specificity
This antibody detects endogenous levels of LAB (Phospho-Tyr136) at Human, Mouse,Rat
Source
Polyclonal, Rabbit,IgG
Formulation
Liquid in PBS containing 50% glycerol, and 0.146% sodium azide.
Dilution rate
WB 1:500-2000
Purification process (Immunogen)
The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
Concentration
1 mg/ml
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
Gene Name
LAT2 LAB NTAL WBS15 WBSCR15 WBSCR5 HSPC046
Protein name
LAB (Phospho-Tyr136)
Abbreviation
LAB
Other 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 15 protein) (Williams-Beuren syndrome chromosomal region 5 protein)
Fields
Human gene ID
7462
Human protein sequence Database
Q9GZY6
Mouse gene ID
56743
Mouse protein sequence database
Q9JHL0
Rat gene ID
317676
Rat protein sequence database
Q8CGL2
Cellular localization
Cell membrane ; Single-pass type III membrane protein . Present in lipid rafts.
Tissue 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).
Storage
-20°C/1 year

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LAB (Phospho-Tyr136) rabbit pAb

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