STX3 Rabbit Polyclonal Antibody, 20ul Centrifuges Defects in this gene are

Defects in this gene are a cause of non-insulin-dependent diabetes mellitus (NIDDM)

CXCL3 encodes a member of the CXC subfamily of chemokines

The protein is also partly localized to the nucleus

which may facilitate formation of heterotrimeric or multiprotein complexes

|tissue specificity:Expressed in all adult human tissues| with 5-fold lower levels observed in the brain

STX3 Rabbit Polyclonal Antibody, 20ul Centrifuges Defects in this gene areThe gene is a member of the syntaxin family. The encoded protein is targeted to the apical membrane of epithelial cells where it forms clusters and is important in establishing and maintaining polarity necessary for protein trafficking involving vesicle fusion and exocytosis. Alternative splicing results in multiple transcript variants.