DGCR2 antibody [N2C1], Internal

GeneTex

DGCR2 antibody [N2C1], Internal

9

Research Use Only

0.48 mg/ml

IgG

Deletions of the 22q11.2 have been associated with a wide range of developmental defects (notably DiGeorge syndrome, velocardiofacial syndrome, conotruncal anomaly face syndrome and isolated conotruncal cardiac defects) classified under the acronym CATCH 22. The DGCR2 gene encodes a novel putative adhesion receptor protein, which could play a role in neural crest cells migration, a process which has been proposed to be altered in DiGeorge syndrome. [provided by RefSeq]

2°C to 8°C,-20°C

12352203