NPC2 rabbit pAb
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],
Product Specifications
Background
UniProt
P61916
Swiss Prot
P61916
Reactivity
Human; Mouse
Immunogen
Synthesized peptide derived from human NPC2 AA range: 9-59
Clonality
Polyclonal
Source
Rabbit
Applications
WB
Concentration
1 mg/ml
Dilution
WB 1: 500-2000
Storage Conditions
-20°C/1 year
Product Datasheet
https://www.elkbiotech.com/upload/file/Antibodies/pAb/ES14462-1.pdf
Fragment
IgG
Subcellular Location
Secreted . Endoplasmic reticulum . Lysosome . Interaction with cell-surface M6PR mediates endocytosis and targeting to lysosomes. .
Gene ID (Human)
10577
Available Sizes
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