PEX1 antibody (AA 1234-1283)

Catalog No. ABIN1535160

This Rabbit Polyclonal antibody specifically detects PEX1 in ELISA, IHC and IF. It exhibits reactivity toward Human and Mouse.

Quick Overview for PEX1 antibody (AA 1234-1283) (ABIN1535160)

Target: PEX1 (Peroxisomal Biogenesis Factor 1 (PEX1))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PEX1 antibody is un-conjugated

Application: ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF)

Product Details anti-PEX1 Antibody

Binding Specificity: AA 1234-1283

Purpose: Peroxin 1 Antibody

Specificity: Peroxin 1 Polyclonal Antibody detects endogenous levels of Peroxin 1 protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Purity: > 95 %

Immunogen: The antiserum was produced against synthesized peptide derived from human PEX1. AA range:1234-1283

Isotype: IgG

Application Details

Application Notes: IHC 1:100 - 1:300. ELISA: 1:10000.. IF 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

Preservative: Sodium azide

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

Storage: -20 °C

Storage Comment: Store at -20°C/1 year

Expiry Date: 12 months

Target Details for PEX1

Target: PEX1 (Peroxisomal Biogenesis Factor 1 (PEX1))

Alternative Name: PEX1

Background:

Synonyms: PEX1, Peroxisome biogenesis factor 1, Peroxin-1, Peroxisome biogenesis disorder protein 1

Background: This gene encodes a member of the AAA ATPase family, a large group of ATPases associated with diverse cellular activities. This protein is cytoplasmic but is often anchored to a peroxisomal membrane where it forms a heteromeric complex and plays a role in the import of proteins into peroxisomes and peroxisome biogenesis. Mutations in this gene have been associated with complementation group 1 peroxisomal disorders such as neonatal adrenoleukodystrophy, infantile Refsum disease, and Zellweger syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2013],

Gene Name: PEX1

Protein Name: Peroxisome biogenesis factor 1

Molecular Weight: 142 kDa

Gene ID: 5189

OMIM: 602136

UniProt: O43933