PEX6 antibody

Catalog No. ABIN2854607

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

Quick Overview for PEX6 antibody (ABIN2854607)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PEX6 antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-PEX6 Antibody

Cross-Reactivity: Human

Characteristics: Rabbit polyclonal antibody to PEX6 (peroxisomal biogenesis factor 6)
PEX6 antibody

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein encompassing a sequence within the center region of human PEX6. The exact sequence is proprietary.

Isotype: IgG

Application Details

Application Notes: WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Comment:

Positive Control: A549

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: 0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal

Preservative: Thimerosal (Merthiolate)

Precaution of Use: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Target Details for PEX6

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

Alternative Name: peroxisomal biogenesis factor 6

Background: This gene 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 this gene cause peroxisome biogenesis disorders of complementation group 4 and complementation group 6.

Cellular Localization: Cytoplasm , Peroxisome membrane

Molecular Weight: 104 kDa

Gene ID: 5190

UniProt: Q13608