PEX12 Antikörper

Produktnummer ABIN7258886

Produktdetails anti-PEX12 Antikörper

Target: PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser PEX12 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein of human PEX12 (NP_000277.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500-1:2000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

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 -20°C. Avoid freeze / thaw cycles.

Details zu PEX12

Target: PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))

Andere Bezeichnung: PEX12 (PEX12 Produkte)

Synonyme: zgc:56182 antikoerper, pex12 antikoerper, MGC81372 antikoerper, PEX12 antikoerper, DDBDRAFT_0186545 antikoerper, DDBDRAFT_0238076 antikoerper, DDB_0186545 antikoerper, DDB_0238076 antikoerper, LOC100226224 antikoerper, PAF-3 antikoerper, PBD3A antikoerper, Peroxin-12 antikoerper, AI451906 antikoerper, peroxisomal biogenesis factor 12 antikoerper, peroxisomal biogenesis factor 12 L homeolog antikoerper, RING zinc finger-containing protein antikoerper, pex12 antikoerper, PEX12 antikoerper, pex12.L antikoerper, Pex12 antikoerper

Hintergrund: This gene belongs to the peroxin-12 family. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of Zellweger syndrome (ZWS).

Molekulargewicht:

Observed_MW: 41 kDa

Calculated_MW: 40 kDa

Gen-ID: 5193

UniProt: O00623