PEX26 antibody (AA 1-265)

Catalog No. ABIN1885866

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

Quick Overview for PEX26 antibody (AA 1-265) (ABIN1885866)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PEX26 antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)

Product Details anti-PEX26 Antibody

Binding Specificity: AA 1-265

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein fragment contain a sequence corresponding to a region within amino acids 1 and 265 of Human PEX26

Application Details

Application Notes: Suggested dilutions:
Western blotting: 1.500-1.3000
Immunohistochemistry: 1.50-1.500
Immunofluorescence: 1.100-1.200

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

Preservative: Thimerosal (Merthiolate)

Precaution of Use: Biohazard Informations: This product contains thimerosal which is hazardous.

Storage: 4 °C/-20 °C

Storage Comment: Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.

Target Details for PEX26

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

Alternative Name: Peroxin 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.[provided by RefSeq]

Molecular Weight: 34 kDa

Gene ID: 55670

NCBI Accession: NP_060399, NM_017929