Arg Monoclonal Antibody, 50ul[BT-MCA0180] Low retention tips Mutations in this gene are

Mutations in this gene are associated with Crouzon syndrome

Alternatively spliced transcript variants have been found for KRT8

and both genes are possible candidates for the autosomal dominant deafness gene (DFNA4)

CYP4F2 encodes a member of the cytochrome P450 superfamily of enzymes

Animal studies also suggest a role for A1 receptors in kidney function and ethanol intoxication

Arg Monoclonal Antibody, 50ul[BT-MCA0180] Low retention tips Mutations in this gene areThis gene encodes a member of the Abelson family of nonreceptor tyrosine protein kinases. The protein is highly similar to the c abl oncogene 1 protein, including the tyrosine kinase, SH2 and SH3 domains, and it plays a role in cytoskeletal rearrangements through its C terminal F actin and microtubule binding sequences. This gene is expressed in both normal and tumor cells, and is involved in translocation with the ets variant 6 gene in leukemia.