DGCR14 Antikörper

Produktnummer ABIN6290316

Produktdetails anti-DGCR14 Antikörper

Target: DGCR14 (DiGeorge Syndrome Critical Region Gene 14 (DGCR14))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser DGCR14 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Aufreinigung: Affinity purification

Immunogen: Recombinant Protein of human DGCR14

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500 - 1:2000

Kommentare:

Highly expressed in heart, brain and skeletal muscle, Detected at low levels in placenta

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20C. Avoid freeze / thaw cycles.

Details zu DGCR14

Target: DGCR14 (DiGeorge Syndrome Critical Region Gene 14 (DGCR14))

Andere Bezeichnung: DGCR14 (DGCR14 Produkte)

Synonyme: DGCR13 antikoerper, DGS-H antikoerper, DGS-I antikoerper, DGSH antikoerper, DGSI antikoerper, ES2 antikoerper, Es2el antikoerper, AI462402 antikoerper, D16H22S1269E antikoerper, Dgcr1 antikoerper, Dgsi antikoerper, fc19d10 antikoerper, wu:fc19d10 antikoerper, zgc:162979 antikoerper, MGC82189 antikoerper, DGCR14 antikoerper, es2 antikoerper, dgsi antikoerper, dgs-h antikoerper, dgs-i antikoerper, es2el antikoerper, dgcr13 antikoerper, ess-2 splicing factor homolog antikoerper, DiGeorge syndrome critical region gene 14 antikoerper, ess-2 splicing factor homolog S homeolog antikoerper, ESS2 antikoerper, Dgcr14 antikoerper, ess2 antikoerper, Ess2 antikoerper, DGCR14 antikoerper, ess2.S antikoerper

Hintergrund: This gene is located within the minimal DGS critical region (MDGCR) thought to contain the gene(s) responsible for a group of developmental disorders. These disorders include DiGeorge syndrome, velocardiofacial syndrome, conotruncal anomaly face syndrome, and some familial or sporadic conotruncal cardiac defects which have been associated with microdeletion of 22q11.2. The encoded protein may be a component of C complex spliceosomes, and the orthologous protein in the mouse localizes to the nucleus. Alternatively spliced transcript variants have been found for this gene.

Molekulargewicht: 52.568 kDa

Gen-ID: 8220

UniProt: Q96DF8