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PEX13 Antibodies

AND PEX13 ELISA kits, PEX13 Proteins

Many biological assays use antibodies to detect PEX13, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with PEX13 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop PEX13 antibodies...

We validate the specificity of these antibodies to PEX13 by testing them on tissues known to express PEX13 positively and negatively. Browse below to find the PEX13 antibody that suites your experiment. We have 2 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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PEX13 Infographic by Boster Bio

PEX13 protein infographic

All PEX13 Products

Filter by Application:

Product

Figures

Specificity

Applications

Price

Anti-PEX13 Antibody

Human, Mouse

ELISA, WB

$380
Cat # A05721
100ul

PEX13 (NM_002618) Human Over-expression Lysate

Human

$628
Cat # LS005194
100 µg

PEX13 Overview

Facts about Peroxisomal membrane protein PEX13.

PEX13 3D structure

PEX13 3D structure. Source: alphafold

Peroxisomal membrane protein PEX13 (PEX13)

Component of the peroxisomal translocation machinery with PEX14 and PEX17.
Functions as a docking factor for the predominantly cytoplasmic PTS1 receptor (PAS10/PEX5).

Involved in the import of PTS1 and PTS2 proteins. .

Gene Information

Human
Gene Name:	PEX13
Uniprot:	Q92968
Entrez:	5194

Gene Information

Family

Belongs to:

peroxin-13 family

Family

Alternative Names

NALD; peroxin-13; peroxisomal biogenesis factor 13; peroxisomal membrane protein PEX13; peroxisome biogenesis factor 13; ZWS

Molecular Weight

Mass (kDA):
44.13 kDA

Molecular Weight

Genomic Context


Human

Location:	2p15
Sequence:	2; NC_000002.12 (61017720..61051990)

Subcellular Localizations

Peroxisome membrane; Single-pass membrane protein.

Subcellular Localization

Diseases

Zellweger Syndrome
Peroxisomal Disorders
Adrenoleukodystrophy
Adrenoleukodystrophy, Neonatal
Disorders Of Peroxisome Biogenesis
Chondrodysplasia Punctata
Neurodegenerative Disorders
Refsum Disease
Muscle Hypotonia
Infantile Refsum Disease (disorder)
Inborn Errors Of Metabolism

Neuronal Migration Disorders
Fetal Growth Retardation
Liver Dysfunction
Chondrodysplasia Punctata, Rhizomelic
Plant Diseases
Gliosis

Disease

Interacting Proteins

PEX19

Interacting Proteins

Pathways

Protein Import
Localization
Transport
Membrane Biogenesis
Protein Transport
Rna Interference
Fatty Acid Oxidation
Cell Migration
Fertilization
Peroxisome Membrane Biogenesis
Dna Repair
Fatty Acid Beta-oxidation
Prenylation

Vesicle Fusion
Reflex
Cerebellum Formation
Translation
Cell Death
Lipid Binding
Membrane Invagination

Pathways

PTMs

Oxidation

Prenylation

Bosterbio | ELISA Kits, Antibodies, Antibody Company

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/PEX13

References

PMID: 9653144 by Fransen M., et al. Identification of a human PTS1 receptor docking protein directly required for peroxisomal protein import.

PMID: 10441330 by Toyama R., et al. Isolation, characterization and mutation analysis of PEX13-defective Chinese hamster ovary cell mutants.