PEX12 Antibodies

AND PEX12 ELISA kits, PEX12 Proteins

Many biological assays use antibodies to detect PEX12, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with PEX12 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop PEX12 antibodies...

We validate the specificity of these antibodies to PEX12 by testing them on tissues known to express PEX12 positively and negatively. Browse below to find the PEX12 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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PEX12 Infographic by Boster Bio

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Anti-Peroxisome assembly protein 12 PEX12 Antibody

Human, Mouse, Rat

ELISA, WB

$380
Cat # A07371
100ul

PEX12 Overview

Facts about Peroxisome assembly protein 12.

PEX12 3D structure. Source: alphafold

Peroxisome assembly protein 12 (PEX12)

Required for protein import into peroxisomes. .

Gene Information

Human
Gene Name:	PEX12
Uniprot:	O00623
Entrez:	5193

Family

Belongs to:

pex2/pex10/pex12 family

Alternative Names

PAF3; PAF-3; peroxin 12; peroxin-12; peroxisomal biogenesis factor 12; Peroxisome assembly factor 3; peroxisome assembly protein 12

Molecular Weight

Mass (kDA):
40.797 kDA

Genomic Context


Human

Location:	17q12
Sequence:	17; NC_000017.11 (35574795..35578571, complement)

Subcellular Localizations

Peroxisome membrane; Multi-pass membrane protein.

Diseases

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

Liver Diseases
Dihydroxycholestanoic Acidemia And Trihydroxycholestanoic Acidemia
Mutation, Out-of-frame
Neurodegenerative Disorders
Ataxia
Neuronal Migration Disorders

Interacting Proteins

PEX19
PEX5

Pathways

Protein Import
Localization
Transport
Membrane Biogenesis
Rna Interference
Protein Targeting
Translation
Meiosis
Fatty Acid Beta-oxidation
Protein Transport
Photorespiration
Karyogamy
Organelle Assembly

Seed Germination
Receptor Recycling
Membrane Docking
Peroxisome Localization
Peroxisome Degradation
Prenylation
Conjugation

PTMs

Oxidation

Ubiquitination

Prenylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/PEX12

References

PMID: 9090384 by Chang C.-C., et al. Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorders.

PMID: 9632816 by Okumoto K., et al. PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12p.