CACNA2D1 Antikörper

Produktnummer ABIN6291847

Produktdetails anti-CACNA2D1 Antikörper

Target: CACNA2D1 (Calcium Channel, Voltage-Dependent, alpha 2/delta Subunit 1 (CACNA2D1))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CACNA2D1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Aufreinigung: Affinity purification

Immunogen: Recombinant protein of human CACNA2D1

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:200 - 1:2000

Kommentare:

Isoform 1 is expressed in skeletal muscle, Isoform 2 is expressed in the central nervous system, Isoform 2, isoform 4 and isoform 5 are expressed in neuroblastoma cells, Isoform 3, isoform 4 and isoform 5 are expressed in the aorta

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 CACNA2D1

Target: CACNA2D1 (Calcium Channel, Voltage-Dependent, alpha 2/delta Subunit 1 (CACNA2D1))

Andere Bezeichnung: CACNA2D1 (CACNA2D1 Produkte)

Synonyme: CACNA2D1 antikoerper, DKFZp469K2211 antikoerper, CACNA2 antikoerper, CACNL2A antikoerper, CCHL2A antikoerper, Ca(v)alpha2delta1 antikoerper, Cacna2 antikoerper, Cchl2a antikoerper, CCHLA2 antikoerper, DHSCCA antikoerper, calcium voltage-gated channel auxiliary subunit alpha2delta 1 antikoerper, calcium channel, voltage-dependent, alpha 2/delta subunit 1 antikoerper, calcium channel, voltage-dependent, alpha2/delta subunit 1 antikoerper, CACNA2D1 antikoerper, cacna2d1 antikoerper, Cacna2d1 antikoerper

Hintergrund: The preproprotein encoded by this gene is cleaved into multiple chains that comprise the alpha-2 and delta subunits of the voltage-dependent calcium channel complex. Calcium channels mediate the influx of calcium ions into the cell upon membrane polarization. Mutations in this gene can cause cardiac deficiencies, including Brugada syndrome and short QT syndrome. Alternate splicing results in multiple transcript variants, some of which may lack the delta subunit portion.

Molekulargewicht: 124.568 kDa

Gen-ID: 781

UniProt: P54289