Tissue expression
Cell line expression
Protein structure

PEX12

Peroxisomal biogenesis factor 12
 
This gene belongs to the peroxin-12 family. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of Zellweger syndrome (ZWS). [provided by RefSeq, Oct 2008]
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136 antibodies from 26 providers.

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AntibodyRefsTypeWBELICCIPIHCFC
Atlas Antibodies
1 antibody
antibodies-online
35 antibodies
Affinity Biosciences
1 antibody
Invitrogen Antibodies
8 antibodies
Novus Biologicals
6 antibodies
Biorbyt
8 antibodies
Abbkine Scientific Co.Ltd.
1 antibody
Boster Biological Technology
1 antibody
Proteintech Group
1 antibody
St John's Laboratory
3 antibodies
Aviva Systems Biology
3 antibodies
Abgent
2 antibodies
Acris Antibodies GmbH
1 antibody
OriGene
1 antibody
Everest Biotech
1 antibody
Creative Diagnostics
4 antibodies
MyBioSource
2 antibodies
United States Biological
25 antibodies
Abbexa
3 antibodies
Leading Biology
2 antibodies
ProSci
2 antibodies
GeneTex
1 antibody
MilliporeSigma / Merck KGaA
1 antibody
Abnova Corporation
4 antibodies
Creative Biolabs
1 antibody