DGCR2 anticorps

N° du produit ABIN2459031

Détail du produit anti-DGCR2 anticorps

Antigène: DGCR2 (DGS2) (DiGeorge Syndrome Chromosome Region-2 (DGS2))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DGCR2 est non-conjugé

Application: Western Blotting (WB), ELISA

Purification: Antibody is purified by peptide affinity chromatography method.

Immunogène: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human DGCR2.

Information d'application

Indications d'application: DGCR2 antibody can be used for detection of DGCR2 by ELISA at 1:62500. DGCR2 antibody can be used for detection of DGCR2 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Concentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Conseil sur la manipulation: As with any antibody avoid repeat freeze-thaw cycles.

Stock: 4 °C/-20 °C

Stockage commentaire: For short periods of storage (days) store at 4 °C. For longer periods of storage, store DGCR2 antibody at -20 °C.

Détails sur DGCR2

Antigène: DGCR2 (DGS2) (DiGeorge Syndrome Chromosome Region-2 (DGS2))

Autre désignation: DGCR2 (DGS2 Produits)

Synonymes: anticorps DGS-C, anticorps IDD, anticorps LAN, anticorps SEZ-12, anticorps CIDD, anticorps 9930034O06Rik, anticorps Dgsc, anticorps Idd, anticorps Lan, anticorps Sez12, anticorps mKIAA0163, anticorps zgc:91974, anticorps DiGeorge syndrome critical region gene 2, anticorps DiGeorge syndrome critical region gene 2 S homeolog, anticorps DGCR2, anticorps Dgcr2, anticorps dgcr2, anticorps dgcr2.S

Sujet: Deletions of the 22q11.2 have been associated with a wide range of developmental defects classified under the acronym CATCH 22. The DGCR2 is 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. 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.

Poids moléculaire: 61 kDa

ID gène: 9993

NCBI Accession: NP_005128

UniProt: P98153