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
Galerie de données de validation
Applications testées
| Résultats positifs en WB | cellules A549, cellules HepG2, cellules HT-1080, tissu pulmonaire de souris, tissu rénal de souris |
| Résultats positifs en IF/ICC | cellules HeLa, |
Dilution recommandée
| Application | Dilution |
|---|---|
| Western Blot (WB) | WB : 1:5000-1:50000 |
| Immunofluorescence (IF)/ICC | IF/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 observé | 17-21 kDa |
| Numéro d’acquisition GenBank | BC002532 |
| 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 stockage | Stocker 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-RR | Download protocol |
| IF protocol for NPC2 antibody 86293-1-RR | Download protocol |
| Standard Protocols | |
|---|---|
| Click here to view our Standard Protocols |


