DGCR2 Antibodies

AND DGCR2 ELISA kits, DGCR2 Proteins

Many biological assays use antibodies to detect DGCR2, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with DGCR2 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop DGCR2 antibodies...

We validate the specificity of these antibodies to DGCR2 by testing them on tissues known to express DGCR2 positively and negatively. Browse below to find the DGCR2 antibody that suites your experiment. We have 0 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

Previous: CCN4 Next: CASP8AP2

DGCR2 Infographic by Boster Bio

All DGCR2 Products

Filter by Application:

Product

Figures

Specificity

Applications

Price

DGCR2 Overview

Facts about Integral membrane protein DGCR2/IDD.

DGCR2 3D structure. Source: alphafold

Integral membrane protein DGCR2/IDD (DGCR2)

Putative adhesion receptor, that could be involved in cell-cell or cell-matrix interactions required for normal cell migration and differentiation. .

Gene Information

Human
Gene Name:	DGCR2
Uniprot:	P98153
Entrez:	9993

Family

Belongs to:

No superfamily

Alternative Names

DGCR2; DGS-C; DiGeorge syndrome critical region gene 2; IDDDKFZp686I1730; integral membrane protein deleted in DiGeorge syndrome; integral membrane protein DGCR2/IDD; KIAA0163; KIAA0163DiGeorge syndrome critical region protein 2; LAN; SEZ-12

Molecular Weight

Mass (kDA):
60.811 kDA

Genomic Context


Human

Location:	22q11.21
Sequence:	22; NC_000022.11 (19036282..19122454, complement)

Subcellular Localizations

Membrane; Single-pass type I membrane protein.

Diseases

Digeorge Syndrome
Schizophrenia
Complete Hearing Loss
Hypoparathyroidism
Haploinsufficiency
Barakat Syndrome
Sensorineural Hearing Loss (disorder)
Monosomy
Renal Dysplasia
Dysplasia
Congenital Heart Defects
Chromosomal Deletion

Cleft Palate
Tissue Adhesions
Diabetes Mellitus, Insulin-dependent
Fracture Of First Cervical Vertebra
Fetal Alcohol Syndrome
Blepharoptosis

Pathways

Transport
Methylation
Stem Cell Differentiation
Thymus Development
Cell Differentiation
Dna Methylation

Eye Development

PTMs

Methylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/DGCR2

References

PMID: 7633403 by Demczuk S., et al. Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinity.

PMID: 7655455 by Wadey R., et al. Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndrome.