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Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
Reconstitute at 0.5 mg/mL in sterile PBS.
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: DGCR2; DGCR2 gene; DiGeorge syndrome critical region protein 2; DiGeorge syndrome gene c; DiGeorge syndrome protein C; integral membrane protein deleted in DiGeorge syndrome; integral membrane protein DGCR2/IDD-like; KIAA0163; seizure-related membrane-bound adhesion protein; unnamed protein product
Gene Aliases: 9930034O06Rik; DGS-C; Dgsc; IDD; LAN; mKIAA0163; SEZ-12; Sez12
UniProt ID: (Human) P98153, (Mouse) P98154
Entrez Gene ID: (Human) 9993, (Mouse) 13356, (Rat) 360742
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