• Phare
  • Validé par KD/KO

Anticorps Polyclonal de lapin anti-NPC1

NPC1 Polyclonal Antibody for FC, IF, IHC, WB, ELISA

Hôte / Isotype

Lapin / IgG

Réactivité testée

Humain, souris et plus (1)

Applications

WB, IHC, IF, FC, ELISA

Conjugaison

Non conjugué

N° de cat : 13926-1-AP

Synonymes

Niemann Pick C1 protein, Niemann Pick disease, type C1, NPC1



Applications testées

Résultats positifs en WBcellules HEK-293 non bouillies, cellules HeLa, cellules HepG2, tissu cérébral de souris non bouilli
Résultats positifs en IHCtissu de cancer du foie humain, tissu cérébral humain, tissu placentaire humain
il est suggéré de démasquer l'antigène avec un tampon de TE buffer pH 9.0; (*) À défaut, 'le démasquage de l'antigène peut être 'effectué avec un tampon citrate pH 6,0.
Résultats positifs en IFcellules HepG2
Résultats positifs en cytométriecellules HepG2,

Dilution recommandée

ApplicationDilution
Western Blot (WB)WB : 1:500-1:2000
Immunohistochimie (IHC)IHC : 1:50-1:500
Immunofluorescence (IF)IF : 1:50-1:500
Flow Cytometry (FC)FC : 0.40 ug per 10^6 cells in a 100 µl suspension
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, check data in validation data gallery

Informations sur le produit

13926-1-AP cible NPC1 dans les applications de WB, IHC, IF, FC, ELISA et montre une réactivité avec des échantillons Humain, souris

Réactivité Humain, souris
Réactivité citéeHumain, porc, souris
Hôte / Isotype Lapin / IgG
Clonalité Polyclonal
Type Anticorps
Immunogène NPC1 Protéine recombinante Ag4946
Nom complet Niemann-Pick disease, type C1
Masse moléculaire calculée 142 kDa
Poids moléculaire observé 160-200 kDa
Numéro d’acquisition GenBankBC063302
Symbole du gène NPC1
Identification du gène (NCBI) 4864
Conjugaison Non conjugué
Forme Liquide
Méthode de purification Purification par affinité contre l'antigène
Tampon de stockage PBS avec azoture de sodium à 0,02 % et glycérol à 50 % pH 7,3
Conditions de stockageStocker à -20°C. Stable pendant un an après l'expédition. L'aliquotage n'est pas nécessaire pour le stockage à -20oC Les 20ul contiennent 0,1% de BSA.

Informations générales

Niemann-Pick Type C (NPC) disease is a lysosomal storage disorder characterized by accumulation of unesterified cholesterol and other lipids in the endolysosomal system. NPC disease results from a defect in either of two distinct cholesterol-binding proteins: a transmembrane protein, NPC1, and a small soluble protein, NPC2. NPC1 or NPC2 deficiency models showed that the functions of these two proteins within lysosomes are linked closely. NPC1 is a typical transmembrane protein and contains a number of modification sites for glycosylation. Defects in NPC1 are the cause of Niemann-Pick disease type C1 which exhibits highly variable clinical phenotype. Moreover, NPC1 may play a role in vesicular trafficking in glia, a process that may be crucial for maintaining the structural and functional integrity of nerve terminals.

Protocole

Product Specific Protocols
WB protocol for NPC1 antibody 13926-1-APDownload protocol
IHC protocol for NPC1 antibody 13926-1-APDownload protocol
IF protocol for NPC1 antibody 13926-1-APDownload protocol
FC protocol for NPC1 antibody 13926-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

Publications

SpeciesApplicationTitle
humanWB

Cell

Cholesterol Transport through Lysosome-Peroxisome Membrane Contacts.

Authors - Bei-Bei Chu
  • KD Validated
humanWB

Nat Commun

A genome-wide CRISPR screen identifies host factors that regulate SARS-CoV-2 entry.

Authors - Yunkai Zhu
humanWB

EMBO J

Insufficiency of ciliary cholesterol in hereditary Zellweger syndrome.

Authors - Tatsuo Miyamoto
  • KO Validated
humanWB

Proc Natl Acad Sci U S A

Cholesterol trafficking is required for mTOR activation in endothelial cells.

Authors - Xu Jing J
  • KD Validated
mouseWB

Proc Natl Acad Sci U S A

Inhibition of sphingolipid synthesis improves outcomes and survival in GARP mutant wobbler mice, a model of motor neuron degeneration.

Authors - Constance S Petit
mouseWB

Cell Rep

The GARP Complex Is Involved in Intracellular Cholesterol Transport via Targeting NPC2 to Lysosomes.

Authors - Jian Wei

Avis

The reviews below have been submitted by verified Proteintech customers who received an incentive forproviding their feedback.


FH

Ganesh (Verified Customer) (02-07-2024)

25 µg of HAP1 (human) whole cell lysate was resolved on a 4-12% Bis-Tris Gel and proteins were transferred onto a nitrocellulose membrane. NPC1 antibody was diluted at 1:1000 in Blocking Buffer (5% Milk in 1x TBS-T (0.1% Tween-20)) and the membrane was incubated overnight at 4 deg C on a rotator.

  • Applications: Western Blot
  • Primary Antibody Dilution: 1:1000
  • Cell Tissue Type: HAP1
NPC1 Antibody Western Blot validation (1:1000 dilution) in HAP1 (Cat no:13926-1-AP)
FH

Benjamin (Verified Customer) (12-09-2021)

Nice antibody that detects Npc1 at the correct molecular weight in primary mouse neurons.

  • Applications: Western Blot
  • Primary Antibody Dilution: 1:1000
  • Cell Tissue Type: Primary Mouse Neurons
NPC1 Antibody Western Blot validation (1:1000 dilution) in Primary Mouse Neurons (Cat no:13926-1-AP)