PEX14 antibody (AA 118-377)

Catalog No. ABIN5704943

The Rabbit Polyclonal anti-PEX14 antibody is suitable to detect PEX14 in samples from Human, Mouse and Rat. It has been validated for WB, ELISA, IHC, IF and IP.

Quick Overview for PEX14 antibody (AA 118-377) (ABIN5704943)

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

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PEX14 antibody is un-conjugated

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

Product Details anti-PEX14 Antibody

Binding Specificity: AA 118-377

Purpose: PEX14 antibody

Immunogen:

Immunogen sequence: 118-377 aa

Immunogen: peroxisomal biogenesis factor 14

Isotype: IgG

Application Details

Application Notes: WB : 1:200-1:1000 IP : 1:200-1:2000 IHC : 1:50-1:200 IF : 1:50-1:500

Comment:

human liver tissue were subjected to SDS PAGE followed by western blot with FNab06327(PEX14 antibody) at dilution of 1:500

Restrictions: For Research Use only

Handling

Buffer: PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handling Advice: Avoid repeated freeze / thaw cycles.

Storage: -20 °C

Storage Comment: -20°C for 12 months

Expiry Date: 12 months

Target Details for PEX14

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

Alternative Name: PEX14

Background:

Synonyms: Peroxisomal membrane protein PEX14|PTS1 receptor-docking protein|Peroxin-14|Peroxisomal membrane anchor protein PEX14|PEX14

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: 57 kDa

Gene ID: 5195

UniProt: O75381

Pathways: Maintenance of Protein Location