PEX3

gene product
The product of this gene is involved in peroxisome biosynthesis and integrity. It assembles membrane vesicles before the matrix proteins are translocated. 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 Zellweger syndrome (ZWS). [provided by RefSeq, Oct 2008]
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Novus Biologicals
5 antibodies
Proteintech Group
1 antibody
Cusabio Biotech Co., Ltd
3 antibodies
Affinity Biosciences
1 antibody
LifeSpan BioSciences, Inc.
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antibodies-online
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Atlas Antibodies
2 antibodies
Biorbyt
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Aviva Systems Biology
2 antibodies
OriGene
2 antibodies
Invitrogen Antibodies
5 antibodies
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2 antibodies
Boster Biological Technology
1 antibody
St John's Laboratory
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ProSci
1 antibody
Abnova Corporation
3 antibodies
Abbkine Scientific Co.Ltd.
1 antibody
Bioworld Technology, Inc
1 antibody
Abbexa
5 antibodies
Creative Diagnostics
4 antibodies
MilliporeSigma / Merck KGaA
4 antibodies
MyBioSource
2 antibodies
United States Biological
13 antibodies
Creative Biolabs
2 antibodies