EPS8 Polyclonal Antibody, 100ul Reservoirs Defects in this gene are

Defects in this gene are a cause of branchiooculofacial syndrome (BOFS)

where its primary property is to respond to the pituitary hormone arginine vasopressin (AVP) by stimulating mechanisms that concentrate the urine and maintain water homeostasis in the organism

Unconventional myosins serve in intracellular movements

the mitogen-activated protein kinase pathway (MAPK) that acts through the ternary complex factors (TCFs)

Seems to be a constitutive component of clathrin-coated pits that is required for receptor-mediated endocytosis

EPS8 Polyclonal Antibody, 100ul Reservoirs Defects in this gene areThis gene encodes a member of the EPS8 family. This protein contains one PH domain and one SH3 domain. It functions as part of the EGFR pathway, though its exact role has not been determined. Highly similar proteins in other organisms are involved in the transduction of signals from Ras to Rac and growth factor mediated actin remodeling. Alternate transcriptional splice variants of this gene have been observed but have not been thoroughly