PEX1 antibody (AA 256-1266) (HRP)

Catalog No. ABIN8020721

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

Quick Overview for PEX1 antibody (AA 256-1266) (HRP) (ABIN8020721)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PEX1 antibody is conjugated to HRP

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC)

Product Details anti-PEX1 Antibody (HRP)

Binding Specificity: AA 256-1266

Purpose: Anti-PEX1 Antibody HRP Conjugated

Cross-Reactivity (Details): No cross-reactivity with other proteins

Predicted Reactivity: Human PEX1 shares 83.4% amino acid (aa) sequence identity with mouse PEX1.

Purification: Immunogen affinity purified.

Immunogen: E.coli-derived human PEX1 recombinant protein (Position: Q256-R1266). Human PEX1 shares 83.4% amino acid (aa) sequence identity with mouse PEX1.

Isotype: IgG

Application Details

Application Notes: Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4.

Storage: -20 °C

Storage Comment: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.

Expiry Date: 12 months

Target Details for PEX1

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

Alternative Name: PEX1

Background:

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.

Gene Full Name: peroxisomal biogenesis factor 1

Gene ID: 5189

UniProt: O43933