AXIN1 Polyclonal Antibody, 50ul Metabolic enzymes differentiation and migration by binding

differentiation and migration by binding to fibroblast growth factors and potentiating their biological effects on target cells

Defects in this gene could be a cause of autosomal dominant coronary artery disease 1 with myocardial infarction (ADCAD1)

|tissue specificity:Expressed in ovarian and colorectal cancer cell lines (at protein level)

Mutations of this gene are associated with autosomal recessive lissencephaly with cerebellar hypoplasia

Isoform 2 and isoform 3 are poorly detected in heart

AXIN1 Polyclonal Antibody, 50ul Metabolic enzymes differentiation and migration by bindingThis gene encodes a cytoplasmic protein which contains a regulation of G protein signaling (RGS) domain and a dishevelled and axin (DIX) domain. The encoded protein interacts with adenomatosis polyposis coli, catenin beta 1, glycogen synthase kinase 3 beta, protein phosphate 2, and itself. This protein functions as a negative regulator of the wingless type MMTV integration site family, member 1 (WNT) signaling pathway and can induce apoptosis. The