SLP-76(Phospho-Tyr145) Rabbit Polyclonal Antibody, 20ul High Speed Micro-Centrifuges a common congenital disorder characterized

a common congenital disorder characterized by neural-crest-related developmental defects

This gene encodes a large coiled coil domain-containing protein that functions in autophagy during starvation conditions

MST1R encodes a cell surface receptor for macrophage-stimulating protein (MSP) with tyrosine kinase activity

function:Polymorphonuclear leukocyte serine protease that degrades elastin

SLP-76(Phospho-Tyr145) Rabbit Polyclonal Antibody, 20ul High Speed Micro-Centrifuges a common congenital disorder characterizedSLP 76 was originally identified as a substrate of the ZAP 70 protein tyrosine kinase following T cell receptor (TCR) ligation in the leukemic T cell line Jurkat. The SLP 76 locus has been localized to human chromosome 5q33 and the gene structure has been partially characterized in mice. The human and murine cDNAs both encode 533 amino acid proteins that are 72% identical and comprised of three modular domains. The NH2 terminus contains an acidic