GSC2 Polyclonal Antibody, 20ul Serum Non-syndromic hearing impairment protein 5

Non-syndromic hearing impairment protein 5 encoded by DFNA5 is expressed in fetal cochlea

and type II deficiency

which is essential for the incorporation of histidine into proteins

Alternatively spliced transcript variants have been described for LAIR2

Excellent mixing (200-1500rpm)

GSC2 Polyclonal Antibody, 20ul Serum Non-syndromic hearing impairment protein 5Goosecoidlike (GSCL), a homeodomain containing gene, resides in the critical region for VCFS DGS on 22q11. Velocardiofacial syndrome (VCFS) is a developmental disorder characterized by conotruncal heart defects, craniofacial anomalies, and learning disabilities. VCFS is phenotypically related to DiGeorge syndrome (DGS) and both syndromes are associated with hemizygous 22q11 deletions. Because many of the tissues and structures affected in VCFS DGS