PEX10 Antikörper

Produktnummer ABIN2458699

Produktdetails anti-PEX10 Antikörper

Target: PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser PEX10 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 PEX10.

Anwendungsinformationen

Applikationshinweise: PEX10 antibody can be used for detection of PEX10 by ELISA at 1:1562500. PEX10 antibody can be used for detection of PEX10 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 PEX10 antibody at -20 °C.

Details zu PEX10

Target: PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))

Andere Bezeichnung: PEX10 (PEX10 Produkte)

Synonyme: ATPEX10 antikoerper, T9J22.2 antikoerper, peroxin 10 antikoerper, NALD antikoerper, PBD6A antikoerper, PBD6B antikoerper, RNF69 antikoerper, AV128229 antikoerper, Gm142 antikoerper, peroxin 10 antikoerper, peroxisomal biogenesis factor 10 antikoerper, PEX10 antikoerper, Pex10 antikoerper

Hintergrund: PEX10 is a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in PEX10 gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome.This gene encodes a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in this gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome. Alternative splicing results in two transcript variants encoding different isoforms.

Molekulargewicht: 37 kDa

Gen-ID: 5192

NCBI Accession: NP_002608

UniProt: O60683

Pathways: Monocarboxylic Acid Catabolic Process