epitope mapping within a C-terminal cytoplasmic domain of DGCR2 of human origin
Modification Notes
DGCR2 (DiGeorge syndrome critical region gene 2), also known as IDD (integral membrane protein, deleted in DGS) is a 550 amino acid single-pass membrane protein that primarily functions as an adhesion receptor and is thought to be involved in cell-matrix or cell-cell interactions, therefore playing an important role in cell migration and differentiation. Due to the chromosomal location of the gene encoding DGCR2, it is suspected that a defect in this gene is involved in the pathogenesis of Digeorge syndrome, also known as velocardiofacial syndrome, which is a complex syndrome involving multiple organs with symptoms such as cardiac defects, cleft palate and a characteristic facial appearance. The chromosomal region of 22q11.21 is also frequently found deleted in schizophrenic patients, suggesting that downregulation of DGCR2 may be implicated in the disease.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFELISA
recommended for detection of DGCR2 of mouse, rat and human origin by WB, IP, IF and ELISA non cross-reactive with DGCR 6 and DGCR 14:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope mapping within a C-terminal cytoplasmic domain of DGCR2 of human origin
Tissue Specificity
epitope mapping within a C-terminal cytoplasmic domain of DGCR2 of human origin