MPV17 rabbit pAb
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MPV17 rabbit pAb
Background:
This gene encodes a mitochondrial inner membrane protein that is implicated in the metabolism of reactive oxygen species. Mutations in this gene have been associated with the hepatocerebral form of mitochondrial DNA depletion syndrome (MDDS) . [provided by RefSeq, Jul 2008]Description:
This gene encodes a mitochondrial inner membrane protein that is implicated in the metabolism of reactive oxygen species. Mutations in this gene have been associated with the hepatocerebral form of mitochondrial DNA depletion syndrome (MDDS). [provided by RefSeq, Jul 2008],UniProt:
P39210Swiss Prot:
P39210Reactivity:
Human; Mouse; RatImmunogen:
Synthesized peptide derived from human MPV17 AA range: 45-95Clonality:
PolyclonalSource:
RabbitApplications:
WBConcentration:
1 mg/mlDilution:
WB 1: 500-2000Storage Conditions:
-20°C/1 yearFragment:
IgGSubcellular Location:
Mitochondrion inner membrane ; Multi-pass membrane protein .Gene ID (Human):
4358
