SPY2 Polyclonal Antibody, 20ul Cell Screening and Imaging Mutations in this gene cause

Mutations in this gene cause congenital heart defects

q14) leading to the fusion of this gene and the MLLT10 gene is found in acute lymphoblastic leukemia

This gene is a putative oncogene encoding a protein belonging to a subfamily of serine/threonine kinases containing SH2-like (Src homology 2-like) domains

breast stomach and pancreas

SPY2 Polyclonal Antibody, 20ul Cell Screening and Imaging Mutations in this gene causeThis gene encodes a protein belonging to the sprouty family. The encoded protein contains a carboxyl terminal cysteine rich domain essential for the inhibitory activity on receptor tyrosine kinase signaling proteins and is required for growth factor stimulated translocation of the protein to membrane ruffles. In primary dermal endothelial cells this gene is transiently upregulated in response to fibroblast growth factor two. This protein is indirectly