PEX10 antibody

Catalog No. ABIN2458699

Product Details anti-PEX10 Antibody

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PEX10 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Purification: Antibody is purified by peptide affinity chromatography method.

Immunogen: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human PEX10.

Application Details

Application Notes: 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.

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Concentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Handling Advice: As with any antibody avoid repeat freeze-thaw cycles.

Storage: 4 °C/-20 °C

Storage Comment: For short periods of storage (days) store at 4 °C. For longer periods of storage, store PEX10 antibody at -20 °C.

Target Details for PEX10

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

Alternative Name: PEX10 (PEX10 Products)

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

Background: 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.

Molecular Weight: 37 kDa

Gene ID: 5192

NCBI Accession: NP_002608

UniProt: O60683

Pathways: Monocarboxylic Acid Catabolic Process