GSC2 Polyclonal Antibody, 20ul Serum and type II deficiency

and type II deficiency

Excellent mixing (200-1500rpm)

FOXD4 encodes a member of the forkhead/winged helix-box (FOX) family of transcription factors

synthetic RNA sequence that directs the Cas9 enzyme to a specific DNA target for cutting

It also lacks the conserved I-helix motif AGX (D

GSC2 Polyclonal Antibody, 20ul Serum and type II deficiencyGoosecoidlike (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