| 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. 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. | 
| Applications: | ELISA, IHC | 
| Name of antibody: | LAT2 | 
| Immunogen: | Fusion protein of human LAT2 | 
| Full name: | linker for activation of T cells family, member 2 | 
| Synonyms: | LAB, NTAL, WSCR5, WBSCR5, HSPC046, WBSCR15 | 
| SwissProt: | Q9GZY6 | 
| ELISA Recommended dilution: | 1000-5000 | 
| IHC positive control: | Human colon cancer | 
| IHC Recommend dilution: | 10-50 | 

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