COL14A1 Polyclonal Antibody, 50ul PCR Series disease:Defects in BMP4 are the

disease:Defects in BMP4 are the cause of microphthalmia syndromic type 6 (MCOPS6)

Mutations in this gene cause spinocerebellar ataxia type 15| a disease associated with an heterogeneous group of cerebellar disorders

a substrate for the epidermal growth factor receptor

TBXAS1 (thromboxane A synthase 1) encodes a member of the cytochrome P450 superfamily of enzymes

which increases in early osteoarthrosis cartilage

COL14A1 Polyclonal Antibody, 50ul PCR Series disease:Defects in BMP4 are theThis gene encodes the alpha chain of type XIV collagen, a member of the FACIT (fibril associated collagens with interrupted triple helices) collagen family. Type XIV collagen interacts with the fibril surface and is involved in the regulation of fibrillogenesis.