PEX26 Antibodies

AND PEX26 ELISA kits, PEX26 Proteins

Many biological assays use antibodies to detect PEX26, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with PEX26 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop PEX26 antibodies...

We validate the specificity of these antibodies to PEX26 by testing them on tissues known to express PEX26 positively and negatively. Browse below to find the PEX26 antibody that suites your experiment. We have 1 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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PEX26 Infographic by Boster Bio

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Human PEX26 Recombinant Protein

SDS-PAGE

$265
Cat # PROTQ7Z412
Starting from 20ug

PEX26 Overview

Facts about Peroxisome assembly protein 26.

PEX26 3D structure. Source: alphafold

Peroxisome assembly protein 26 (PEX26)

Likely required for protein import into peroxisomes. Anchors PEX1 and PEX6 to peroxisome membranes, possibly to form heteromeric AAA ATPase complexes necessary for the import of proteins into peroxisomes.

Involved in the import of catalase and proteins comprising a PTS2 target sequence, but not in import of proteins with a PTS1 target sequence. .

Gene Information

Human
Gene Name:	PEX26
Uniprot:	Q7Z412
Entrez:	55670

Family

Belongs to:

peroxin-26 family

Alternative Names

FLJ20695; peroxin-26; peroxisomal biogenesis factor 26; peroxisome assembly protein 26; peroxisome biogenesis disorder, complementation group 8; peroxisome biogenesis disorder, complementation group A; peroxisome biogenesis factor 26; PEX26M1T; Pex26pM1T

Molecular Weight

Mass (kDA):
33.898 kDA

Genomic Context


Human

Location:	22q11.21
Sequence:	22; NC_000022.11 (18077990..18105396)

Tissue Specificity

Widely expressed. Highly expressed in kidney, liver, brain and skeletal muscles. Expressed at intermediate level in pancreas, placenta and heart. Weakly expressed in lung.

Subcellular Localizations

Peroxisome membrane; Single-pass type II membrane protein.

Diseases

Disorders Of Peroxisome Biogenesis
Zellweger Syndrome
Aortic Aneurysm, Abdominal
Peroxisomal Disorders
Adrenoleukodystrophy, Neonatal
Adrenoleukodystrophy
Refsum Disease
Infantile Refsum Disease (disorder)
Apnea
Myeloproliferative Syndrome, Transient
Optic Atrophy

Neurodegenerative Disorders
Atrophy
De Novo Mutation
Muscle Hypotonia
Epilepsy
Cryptorchidism

Interacting Proteins

PEX19
SUFU

Pathways

Localization
Transport
Protein Import
Organelle Assembly
Fertilization
Proteolysis
Protein Transport

Rna Interference

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/PEX26

References

PMID: 12717447 by Matsumoto N., et al. The pathogenic peroxin Pex26p recruits the Pex1p-Pex6p AAA ATPase complexes to peroxisomes.

PMID: 12851857 by Matsumoto N., et al. Mutations in novel peroxin gene PEX26 that cause peroxisome- biogenesis disorders of complementation group 8 provide a genotype- phenotype correlation.