BMPR-II Rabbit Polyclonal Antibody, 20ul[BT-AP06581] Nucleic Acid Extraction 32 and 14 kDa chains

32 and 14 kDa chains

Defects in POU4F3 are the cause of non-syndromic sensorineural deafness autosomal dominant type 15

Rotor capacity: 2mL/1

The protein is expressed in the photoreceptor layer of the retina| and the gene is mutated in autosomal recessive retinitis pigmentosa

carpal tunnel syndrome

BMPR-II Rabbit Polyclonal Antibody, 20ul[BT-AP06581] Nucleic Acid Extraction 32 and 14 kDa chainsThis gene encodes a member of the bone morphogenetic protein (BMP) receptor family of transmembrane serine threonine kinases. The ligands of this receptor are BMPs which are members of the TGF beta superfamily. BMPs are involved in endochondral bone formation and embryogenesis. These proteins transduce their signals through the formation of heteromeric complexes of two different types of serine (threonine) kinase receptors: type I receptors of about