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PEX10
Peroxisomal biogenesis factor 10RNF69
This gene encodes a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in this gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome. Alternative splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
Top validated antibodies |
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| antibodies-online |  ABIN310466 |
1 references | Polyclonal |
WB
IHC
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| Affinity Biosciences | DF4288 |
Polyclonal |
WB
EL
ICC
IHC
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| LSBio | LS-C120207 |
Polyclonal |
WB
EL
IHC
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| Invitrogen Antibodies | PA5-101746 |
Polyclonal |
WB
ICC
IHC
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| St John's Laboratory | STJ95035 |
Polyclonal |
WB
EL
ICC
IHC
|
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