DGCR2 Antikörper

Produktnummer ABIN2459031

Produktdetails anti-DGCR2 Antikörper

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

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser DGCR2 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Aufreinigung: Antibody is purified by peptide affinity chromatography method.

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

Anwendungsinformationen

Applikationshinweise: 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.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Lyophilized

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

Konzentration: 1 mg/mL

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

Handhabung: As with any antibody avoid repeat freeze-thaw cycles.

Lagerung: 4 °C/-20 °C

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

Details zu DGCR2

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

Andere Bezeichnung: DGCR2 (DGS2 Produkte)

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

Hintergrund: 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.

Molekulargewicht: 61 kDa

Gen-ID: 9993

NCBI Accession: NP_005128

UniProt: P98153