PEX26 antibody

Catalog No. ABIN2856684

This anti-PEX26 antibody is a Rabbit Polyclonal antibody detecting PEX26 in WB, ICC, IHC (p) and IF. Suitable for Human.

Quick Overview for PEX26 antibody (ABIN2856684)

Target: PEX26 (Peroxisomal Biogenesis Factor 26 (PEX26))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PEX26 antibody is un-conjugated

Application: Western Blotting (WB), Immunocytochemistry (ICC), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (IF)

Product Details anti-PEX26 Antibody

Cross-Reactivity: Human

Characteristics: Rabbit Polyclonal antibody to PEX26 (peroxisomal biogenesis factor 26)
PEX26 antibody

Purification: Purified by antigen-affinity chromatography.

Immunogen: Full length human PEX26 Recombinant protein.

Isotype: IgG

Application Details

Application Notes: WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Comment:

Positive Control: A431

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 PEX26

Target: PEX26 (Peroxisomal Biogenesis Factor 26 (PEX26))

Alternative Name: peroxisomal biogenesis factor 26

Background: This gene belongs to the peroxin-26 gene family. It is probably required for protein import into peroxisomes. It anchors PEX1 and PEX6 to peroxisome membranes, possibly to form heteromeric AAA ATPase complexes required for the import of proteins into peroxisomes. Defects in this gene are the cause of peroxisome biogenesis disorder complementation group 8 (PBD-CG8). PBD refers to a group of peroxisomal disorders arising from a failure of protein import into the peroxisomal membrane or matrix. The PBD group is comprised of four disorders: Zellweger syndrome (ZWS), neonatal adrenoleukodystrophy (NALD), infantile Refsum disease (IRD), and classical rhizomelic chondrodysplasia punctata (RCDP). Two transcript variants encoding the same protein have been identified for this gene.

Cellular Localization: Peroxisome membrane, Single-pass type II membrane protein

Molecular Weight: 34 kDa

Gene ID: 55670

UniProt: Q7Z412