PEX12 Antikörper (AA 131-158)

Produktnummer ABIN5532645

Produktdetails anti-PEX12 Antikörper

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

Bindungsspezifität: AA 131-158

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser PEX12 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Aufreinigung: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This PEX12 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 131-158 amino acids from the Central region of human PEX12.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: For WB starting dilution is: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.5 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) sodium azide.

Konservierungsmittel: Sodium azide

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

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: 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.

Molekulargewicht: 41 kDa

Gen-ID: 5193

UniProt: O00623