NPC2 rabbit pAb
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NPC2 rabbit pAb
Background:
This gene encodes a protein containing a lipid recognition domain. The encoded protein may function in regulating the transport of cholesterol through the late endosomal/lysosomal system. Mutations in this gene have been associated with Niemann-Pick disease, type C2 and frontal lobe atrophy. [provided by RefSeq, Jul 2008]Description:
This gene encodes a protein containing a lipid recognition domain. The encoded protein may function in regulating the transport of cholesterol through the late endosomal/lysosomal system. Mutations in this gene have been associated with Niemann-Pick disease, type C2 and frontal lobe atrophy. [provided by RefSeq, Jul 2008],UniProt:
P61916Swiss Prot:
P61916Reactivity:
Human; MouseImmunogen:
Synthesized peptide derived from human NPC2 AA range: 9-59Clonality:
PolyclonalSource:
RabbitApplications:
WBConcentration:
1 mg/mlDilution:
WB 1: 500-2000Storage Conditions:
-20°C/1 yearFragment:
IgGSubcellular Location:
Secreted . Endoplasmic reticulum . Lysosome . Interaction with cell-surface M6PR mediates endocytosis and targeting to lysosomes. .Gene ID (Human):
10577
