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SLC25A15
Solute carrier family 25 member 15D13S327, HHH, ORC1, ORNT1
This gene is a member of the mitochondrial carrier family. The encoded protein transports ornithine across the inner mitochondrial membrane from the cytosol to the mitochondrial matrix. The protein is an essential component of the urea cycle, and functions in ammonium detoxification and biosynthesis of the amino acid arginine. Mutations in this gene result in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome. There is a pseudogene of this locus on the Y chromosome. [provided by RefSeq, May 2009]
Top validated antibodies |
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| Invitrogen Antibodies |  PA5-118265 |
Polyclonal |
WB
IP
IHC
OA
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| Novus Biologicals | NBP2-20387 |
2 references | Polyclonal |
WB
IHC
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| Proteintech Group | 15317-1-AP |
Polyclonal |
WB
EL
IHC
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| NovoPro Bioscience Inc. | 115324 |
Polyclonal |
WB
EL
IHC
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| Cusabio Biotech Co., Ltd | CSB-PA021481GA01HU |
Polyclonal |
WB
EL
IHC
|
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