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NPC1 Antibody / Niemann Pick C1

This gene encodes a large protein that resides in the limiting membrane of endosomes and lysosomes and mediates intracellular cholesterol trafficking via binding of cholesterol to its N-terminal domain. It is predicted to have a cytoplasmic C-terminus, 13 transmembrane domains, and 3 large loops in the lumen of the endosome - the last loop being at the N-terminus. This protein transports low-density lipoproteins to late endosomal/lysosomal compartments where they are hydrolized and released as free cholesterol. Defects in this gene cause Niemann-Pick type C disease, a rare autosomal recessive neurodegenerative disorder characterized by over accumulation of cholesterol and glycosphingolipids in late endosomal/lysosomal compartments.

Product Specifications

CAS Number

9007-83-4

Specifications

Western blot: 1:1000, Immunofluorescence: 1:10-1:50, Immunohistochemistry (Paraffin) : 1:10-1:50

UniProt

O15118

Host

Rabbit

Reactivity

Human

Immunogen

A portion of amino acids 591-620 from the human protein was used as the immunogen for this NPC1 antibody.

Clonality

Polyclonal

Isotype

Ig

Applications

IF, IHC, WB, ELISA

Purity

Antigen affinity

Format

Antigen affinity purified

Buffer

In 1X PBS, pH 7.4, with 0.09% sodium azide

Reconstitution

Aliquot the NPC1 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Limitations

This NPC1 antibody is available for research use only.

Storage Conditions

Aliquot the NPC1 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.

Formulation

In 1X PBS, pH 7.4, with 0.09% sodium azide

Applications Notes

Titration of the NPC1 antibody may be required due to differences in protocols and secondary/substrate sensitivity.

Image Legend

NPC1 antibody western blot analysis in NCI-H460 lysate. Predicted molecular weight ~142/170~190 kDa (unmodified/glycosylated) .

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