PEX1 antibody (AA 1210-1290)

Catalog No. ABIN7223120

The Rabbit Polyclonal anti-PEX1 antibody is suitable to detect PEX1 in samples from Human and Mouse. It has been validated for ELISA, IHC and IF.

Quick Overview for PEX1 antibody (AA 1210-1290) (ABIN7223120)

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 1210-1290

Purpose: Rabbit Anti-Peroxin 1 Polyclonal 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.

Immunogen: Synthesized peptide derived from the C-terminal region of human Peroxin 1 at AA range: 1210-1290

Isotype: IgG

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: 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: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Expiry Date: 12 months

Target Details for PEX1

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

Alternative Name: Peroxin 1

Background: PEX1, Peroxisome biogenesis factor 1, Peroxin-1, Peroxisome biogenesis disorder protein 1PEX1 (peroxisomal biogenesis factor 1) 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 PEX1 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.

Gene ID: 5189

UniProt: O43933