AT132 rabbit pAb
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AT132 rabbit pAb
Background :
This gene encodes a member of the P5 subfamily of ATPases which transports inorganic cations as well as other substrates. Mutations in this gene are associated with Kufor-Rakeb syndrome (KRS), also referred to as Parkinson disease 9. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Nov 2008]Description :
This gene encodes a member of the P5 subfamily of ATPases which transports inorganic cations as well as other substrates. Mutations in this gene are associated with Kufor-Rakeb syndrome (KRS), also referred to as Parkinson disease 9. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2008],UniProt :
Q9NQ11Swiss Prot :
Q9NQ11Reactivity :
Human; MouseImmunogen :
Synthesized peptide derived from human AT132 AA range: 56-106Target :
AT132Clonality :
PolyclonalSource :
RabbitApplications :
WBConcentration :
1 mg/mlDilution :
WB 1:500-2000Buffer :
-20°C/1 yearStorage Conditions :
-20°C/1 yearFragment :
IgGSubcellular Location :
Lysosome membrane ; Multi-pass membrane protein . Late endosome membrane ; Multi-pass membrane protein . Endosome, multivesicular body membrane ; Multi-pass membrane protein . Cytoplasmic vesicle, autophagosome membrane ; Multi-pass membrane protein .Gene ID (Human) :
23400

