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

Cyclin-dependent kinase 4 encoded by CDK4 is a member of the Ser/Thr protein kinase family

Take your experiments to the next level and conquer new scientific frontiers with MetaCell®CHO-100

and type II deficiency

It contains four active calcium-binding domains

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