Niemann-Pick Disease, Type C1 Proteine (NPC1)

NPC1 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. Zusätzlich bieten wir Ihnen NPC1 Antikörper (73) und NPC1 Kits (5) und viele weitere Produktgruppen zu diesem Protein an.

alle Proteine anzeigen Gen GeneID UniProt
NPC1 18145 O35604
NPC1 4864 O15118
Ratte NPC1 NPC1 266732  
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Top NPC1 Proteine auf antikoerper-online.de

Showing 6 out of 10 products:

Katalog Nr. Origin Quelle Konjugat Bilder Menge Anbieter Lieferzeit Preis Details
Escherichia coli (E. coli) Maus His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Anmelden zum Anzeigen 30 bis 35 Tage
$4,331.68
Details
Escherichia coli (E. coli) Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Anmelden zum Anzeigen 30 bis 35 Tage
$4,331.68
Details
Insektenzellen Maus His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Anmelden zum Anzeigen 50 Days
$5,442.50
Details
Insektenzellen Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Anmelden zum Anzeigen 50 Days
$5,442.50
Details
Human Cells Human DYKDDDDK Tag,His tag SDS-PAGE 100 μg Anmelden zum Anzeigen 20 bis 21 Tage
$437.80
Details
Wheat germ Human GST tag 10 μg Anmelden zum Anzeigen 11 bis 12 Tage
$405.71
Details

NPC1 Proteine nach Spezies und Herkunft

Origin Exprimiert in Konjugat
Mouse (Murine) ,
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Human , , ,
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Weitere Proteine zu Niemann-Pick Disease, Type C1 (NPC1) Interaktionspartnern

Zebrafish Niemann-Pick Disease, Type C1 (NPC1) Interaktionspartner

  1. this is the first report, showing a role of NPC1 in platelet function and formation but further studies are needed to define how cholesterol storage interferes with these processes

  2. npc1 is required early for proper cell movement and cholesterol localization and later for cell survival

Rabbit Niemann-Pick Disease, Type C1 (NPC1) Interaktionspartner

  1. Availability of assays to measure NPC1 binding to membrne proteins may further the understanding of ways in which oxysterols regulate intracellular lipid transport.

Mouse (Murine) Niemann-Pick Disease, Type C1 (NPC1) Interaktionspartner

  1. Lysosomal oxLDL accumulation within macrophages contributes to murine atherosclerosis. Prevention of oxLDL uptake leads to decreased atherosclerosis in hematopoietic NPC1-deficient Ldlr (zeige LDLR Proteine)(-/-) mice

  2. the spleen is significantly enlarged in Npc1(-/-) mice.

  3. Study is the first data to reveal motor and behavioral deficits in early maturity of Npc1+/- mice.

  4. Npc1 gene interacts with a high fat diet to promote weight gain through differential regulation of central energy metabolism pathways.

  5. AAV9-mediated NPC1 delivery significantly promoted Purkinje cell survival, restored locomotor activity and coordination, and increased the lifespan of NPC1(-/-) mice. Our work suggests that AAV-based gene therapy is a promising means to treat NPC disease.

  6. Here, we identify lamellar inclusions as the subcellular site of lipid accumulation in neurons, we uncover a vicious cycle of cholesterol synthesis and accretion, which may cause gradual neurodegeneration, and we reveal how beta-cyclodextrin, a potential therapeutic drug, reverts these changes. Our study provides new mechanistic insight in NPC disease and uncovers new targets for therapeutic approaches.

  7. Male NPC1+/- mice had increased fat storage while eating a high-fat diet.

  8. Our data show that: i) HDAC2 (zeige HDAC2 Proteine) levels and activity are increased in NPC neuronal models and in Npc1(-/-) mice; ii) inhibition of c-Abl (zeige ABL1 Proteine) or c-Abl (zeige ABL1 Proteine) deficiency prevents the increase of HDAC2 (zeige HDAC2 Proteine) protein levels and activity in NPC neuronal models

  9. This study showed that deleting the Npc1 gene is accompanied by an increase in germ cell apoptosis and compensatory imbalances in the expression of cholesterol enzymatic and transporter factors.

  10. These results show that NPC1 is critical for ebolavirus replication and pathogenesis in animals.

Human Niemann-Pick Disease, Type C1 (NPC1) Interaktionspartner

  1. We identified major events in NPC1 evolution and revealed and compared orthologs and paralogs of the human NPC1 gene through phylogenetic and protein sequence analyses. We predicted whether an amino acid substitution affects protein function by reducing the organism's fitness.

  2. The mutant NPC1 did not significantly reduce cholesterol accumulation, but approximately 85% of the mutants showed reduced cholesterol accumulation when treated with vorinostat or panobinostat.

  3. knockdown of TMEM97 (zeige TMEM97 Proteine) also increases levels of residual NPC1 in NPC1-mutant patient fibroblasts and reduces cholesterol storage in an NPC1-dependent manner. Our findings propose TMEM97 (zeige TMEM97 Proteine) inhibition as a novel strategy to increase residual NPC1 levels in cells and a potential therapeutic target for Niemann-Pick type C disease (NP-C).

  4. Rare loss-of-function NPC1 mutations were identified as being associated with human adiposity with a high penetrance in a Chinese population.

  5. Furthermore saturation and intracellular distribution of alpha-Toc (zeige RHBDF2 Proteine) seem to be strongly dependent on the availability of this vitamin as well as on the presence of the lysosomal protein NPC1

  6. Two mutations were identified in the NPC1 gene, one of which was novel and its pathogenetic nature was unknown

  7. Our data suggest an incidence rate for NPC1 and NPC2 (zeige NPC2 Proteine) of 1/92,104 and 1/2,858,998, respectively. Evaluation of common NPC1 variants, however, suggests that there may be a late-onset NPC1 phenotype with a markedly higher incidence.

  8. Fibroblasts from Niemann-Pick type C (NPC) disease patients with low levels of NPC1 protein have high amounts of procathepsin D but reduced quantities of the mature protein, thus showing a diminished cathepsin D (zeige CTSD Proteine) activity.

  9. Results identified six novel mutations (PKHD1: p.Thr777Met, p.Tyr2260Cys; ABCB11 (zeige ABCB11 Proteine): p.Val1112Phe, c.611+1G > A, p.Gly628Trpfs*3 and NPC1: p.Glu391Lys) for the diagnostic of inherited infantile cholestatic disorders.

  10. NPC1 mutations are substantially enriched in unexplained early onset ataxia, making it high risk group for Niemann-Pick disease type C.

NPC1 Protein Überblick

Protein Überblick

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.

Genbezeichner und Symbole assoziert mit NPC1

  • NPC intracellular cholesterol transporter 1 (NPC1)
  • Niemann-Pick disease, type C1 (npc1)
  • Niemann-Pick C1 protein (LOC579887)
  • NPC intracellular cholesterol transporter 1 (Npc1)
  • A430089E03Rik Protein
  • C85354 Protein
  • Cdig2 Protein
  • D18Ertd139e Protein
  • D18Ertd723e Protein
  • im:7149020 Protein
  • lcsd Protein
  • nmf164 Protein
  • NPC Protein
  • spm Protein
  • wu:fb53a12 Protein
  • wu:fc29a12 Protein

Bezeichner auf Proteinebene für NPC1

Niemann-Pick C1 protein , Niemann-Pick type C1 disease protein , Nasopharyngeal carcinoma 1 , Niemann-Pick C1 , Niemann-Pick disease, type C1 , sphingomyelinosis , Niemann-Pick C disease protein

GENE ID SPEZIES
403698 Canis lupus familiaris
455338 Pan troglodytes
493693 Felis catus
553330 Danio rerio
579887 Strongylocentrotus purpuratus
100008746 Oryctolagus cuniculus
18145 Mus musculus
4864 Homo sapiens
397591 Sus scrofa
421076 Gallus gallus
266732 Rattus norvegicus
100718604 Cavia porcellus
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