PEX1 antibody (AA 256-1266)

Catalog No. ABIN8020725

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

Quick Overview for PEX1 antibody (AA 256-1266) (ABIN8020725)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PEX1 antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Flow Cytometry (FACS), Immunofluorescence (IF)

Grade: Carrier-free

Product Details anti-PEX1 Antibody

Binding Specificity: AA 256-1266

Purpose: Anti-PEX1 Antibody

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

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

Characteristics: Anti-PEX1 Antibody. Tested in WB, IHC, IF, Flow Cytometry, ELISA applications. This antibody reacts with Human.

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, 0.25-0.5 μg/mL, Human Immunohistochemistry (Paraffin-embedded Section), 2-5 μg/mL, Human Immunofluorescence, 5 μg/mL, Human Flow Cytometry (Fixed), 1-3 μg/1x10⁶ cells, Human ELISA, 0.1-0.5 μg/mL

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Storage: 4 °C,-20 °C

Storage Comment: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. 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

Molecular Weight: 143 kDa

Gene ID: 5189

UniProt: O43933