HPS6 rabbit pAb
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HPS6 rabbit pAb
Background :
This intronless gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. This protein interacts with Hermansky-Pudlak syndrome 5 protein. Mutations in this gene are associated with Hermansky-Pudlak syndrome type 6. [provided by RefSeq, Jul 2008]Description :
This intronless gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. This protein interacts with Hermansky-Pudlak syndrome 5 protein. Mutations in this gene are associated with Hermansky-Pudlak syndrome type 6. [provided by RefSeq, Jul 2008],UniProt :
Q86YV9Swiss Prot :
Q86YV9Reactivity :
Human; Mouse; RatImmunogen :
Synthesized peptide derived from human HPS6 AA range: 168-218Target :
HPS6Clonality :
PolyclonalSource :
RabbitApplications :
WBConcentration :
1 mg/mlDilution :
WB 1:500-2000Buffer :
-20°C/1 yearStorage Conditions :
-20°C/1 yearFragment :
IgGSubcellular Location :
Microsome membrane . Cytoplasm, cytosol . Early endosome membrane . Lysosome membrane .Gene ID (Human) :
79803

