Anticorps Recombinant de lapin anti-NPC2

NPC2 Recombinant Antibody for WB, IF/ICC, ELISA

Hôte / Isotype

Lapin / IgG

Réactivité testée

Humain, souris

Applications

WB, IF/ICC, ELISA

Conjugaison

Non conjugué

CloneNo.

250911E11

N° de cat : 86293-1-RR

Synonymes

He1, Human epididymis-specific protein 1, Niemann-Pick disease type C2 protein



Applications testées

Résultats positifs en WBcellules A549, cellules HepG2, cellules HT-1080, tissu pulmonaire de souris, tissu rénal de souris
Résultats positifs en IF/ICCcellules HeLa,

Dilution recommandée

ApplicationDilution
Western Blot (WB)WB : 1:5000-1:50000
Immunofluorescence (IF)/ICCIF/ICC : 1:250-1:1000
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

86293-1-RR cible NPC2 dans les applications de WB, IF/ICC, ELISA et montre une réactivité avec des échantillons Humain, souris

Réactivité Humain, souris
Hôte / Isotype Lapin / IgG
Clonalité Recombinant
Type Anticorps
Immunogène NPC2 Protéine recombinante Ag13719
Nom complet Niemann-Pick disease, type C2
Masse moléculaire calculée 151 aa, 17 kDa
Poids moléculaire observé17-21 kDa
Numéro d’acquisition GenBankBC002532
Symbole du gène NPC2
Identification du gène (NCBI) 10577
Conjugaison Non conjugué
Forme Liquide
Méthode de purification Purification par protéine A
Tampon de stockage PBS with 0.02% sodium azide and 50% glycerol
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 function of these two proteins within lysosomes are linked closely. NPC2 is also named human epididymis-specific protein 1 (HE1), defects of which are the cause of Niemann-Pick disease type C2, characterized as a lysosomal storage disorder that affects the viscera and the central nervous system. Recent finding suggests that NPC2 may serve as a novel intracrine/autocrine factor that controls adipocyte differentiation and function as well as potential therapeutic target for the treatment of type 2 diabetes and related metabolic disorders.

Protocole

Product Specific Protocols
WB protocol for NPC2 antibody 86293-1-RRDownload protocol
IF protocol for NPC2 antibody 86293-1-RRDownload protocol
Standard Protocols
Click here to view our Standard Protocols
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