TSH3 Polyclonal Antibody, 20ul Plates & Dishes The gene is deleted in

The gene is deleted in Williams-Beuren syndrome| a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11

It is thought to mediate calcineurin inhibition

NF-kappa-B is composed of NFKB1 or NFKB2 bound to either REL

The protein product of this gene

the first laminin isolated from Engelbreth-Holm-Swarm (EHS) tumor

TSH3 Polyclonal Antibody, 20ul Plates & Dishes The gene is deleted inThis gene encodes a zinc finger transcription factor that regulates smooth muscle cell differentiation in the developing urinary tract. Consistent with this role, mice in which this gene has been inactivated exhibit abnormal gene expression in urinary tract smooth muscle cell precursors and kidney defects including hydronephrosis. The encoded transcription factor comprises a gene silencing complex that inhibits caspase expression. Reduced expression