PEX14 antibody (AA 121-150)

Catalog No. ABIN656491

Product Details anti-PEX14 Antibody

Target: PEX14 (Peroxisomal Biogenesis Factor 14 (PEX14))

Binding Specificity: AA 121-150

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PEX14 antibody is un-conjugated

Application: Western Blotting (WB), Flow Cytometry (FACS)

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This PEX14 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 121-150 amino acids from the Central region of human PEX14.

Clone: RB31100

Isotype: Ig Fraction

Application Details

Application Notes: WB: 1:1000. FC: 1:10~50

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

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: 4 °C,-20 °C

Storage Comment: PEX14 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

Expiry Date: 6 months

Target Details for PEX14

Target: PEX14 (Peroxisomal Biogenesis Factor 14 (PEX14))

Alternative Name: PEX14 (PEX14 Products)

Synonyms: ATPEX14 antibody, MQB2.13 antibody, MQB2_13 antibody, PED2 antibody, PEROXISOME DEFECTIVE 2 antibody, peroxin 14 antibody, NAPP2 antibody, PBD13A antibody, Pex14p antibody, dJ734G22.2 antibody, R75137 antibody, peroxisomal biogenesis factor 14 antibody, peroxin 14 antibody, PEX14 antibody, Pex14 antibody

Background: This gene encodes an essential component of the peroxisomal import machinery. The protein is integrated into peroxisome membranes with its C-terminus exposed to the cytosol, and interacts with the cytosolic receptor for proteins containing a PTS1 peroxisomal targeting signal. The protein also functions as a transcriptional corepressor and interacts with a histone deacetylase. A mutation in this gene results in one form of Zellweger syndrome.

Molecular Weight: 41237

Gene ID: 5195

NCBI Accession: NP_004556

UniProt: O75381

Pathways: Maintenance of Protein Location