PEX6 antibody (AA 480-560)

Catalog No. ABIN7230598

The Rabbit Polyclonal anti-PEX6 antibody is suitable to detect PEX6 in samples from Human, Rat and Mouse. It has been validated for WB and ELISA.

Quick Overview for PEX6 antibody (AA 480-560) (ABIN7230598)

Target: PEX6 (Peroxisomal Biogenesis Factor 6 (PEX6))

Reactivity: Human, Rat, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PEX6 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-PEX6 Antibody

Binding Specificity: AA 480-560

Purpose: PEX6 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of PEX6 protein

Purification: The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

Immunogen: Synthesized peptide derived from part region of human PEX6 protein at AA range: 480-560

Isotype: IgG

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

Comment:

Primary Antibody

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

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.

Target Details for PEX6

Target: PEX6 (Peroxisomal Biogenesis Factor 6 (PEX6))

Alternative Name: PEX6

Background: Rabbit Anti-PEX6 Polyclonal Antibody,Peroxisome assembly factor 2, PAF-2, Peroxin-6, Peroxisomal biogenesis factor 6, Peroxisomal-type ATPase 1,PEX6 (Peroxisomal Biogenesis Factor 6) is a Protein Coding gene. Diseases associated with PEX6 include Peroxisome Biogenesis Disorder 4A and Heimler Syndrome 2. Among its related pathways are Peroxisome. PEX6 encodes a member of the AAA (ATPases associated with diverse cellular activities) family of ATPases. This member is a predominantly cytoplasmic protein, which plays a direct role in peroxisomal protein import and is required for PTS1 (peroxisomal targeting signal 1, a C-terminal tripeptide of the sequence ser-lys-leu) receptor activity. Mutations in PEX6 cause peroxisome biogenesis disorders of complementation group 4 and complementation group 6. Several transcript variants encoding different isoforms have been found for PEX6.,PEX6

Molecular Weight: observerd band 107kDa

Gene ID: 5190

UniProt: Q13608