PEX1 antibody (Middle Region)

Catalog No. ABIN954094

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

Quick Overview for PEX1 antibody (Middle Region) (ABIN954094)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PEX1 antibody is un-conjugated

Application: Western Blotting (WB), Enzyme Immunoassay (EIA)

Product Details anti-PEX1 Antibody

Binding Specificity: AA 606-637, Middle Region

Specificity: This antibody recognizes Human Peroxin 1 / PEX1 (Center).

Purification: Protein A column, followed by peptide affinity purification

Immunogen: KLH conjugated synthetic peptide between 606-637 amino acids from the Central region of Human Peroxin 1 / PEX1

Isotype: Ig Fraction

Application Details

Application Notes: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: PBS containing 0.09 % (W/V) Sodium Azide as preservative

Preservative: Sodium azide

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

Handling Advice: Avoid repeated freezing and thawing.

Storage: 4 °C/-20 °C

Storage Comment: Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Target Details for PEX1

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

Alternative Name: Peroxin 1 / PEX1

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

Molecular Weight: 142867 Da

Gene ID: 5189

NCBI Accession: NP_000457