- Phare
- Validé par KD/KO
Anticorps Polyclonal de lapin anti-AP3B1
AP3B1 Polyclonal Antibody for WB, IHC, IP, Indirect ELISA
Hôte / Isotype
Lapin / IgG
Réactivité testée
Humain, rat, souris
Applications
WB, IHC, IP, Indirect ELISA
Conjugaison
Non conjugué
N° de cat : 13384-1-PBS
Synonymes
Galerie de données de validation
Informations sur le produit
13384-1-PBS cible AP3B1 dans les applications de WB, IHC, IP, Indirect ELISA et montre une réactivité avec des échantillons Humain, rat, souris
| Réactivité | Humain, rat, souris |
| Hôte / Isotype | Lapin / IgG |
| Clonalité | Polyclonal |
| Type | Anticorps |
| Immunogène | AP3B1 Protéine recombinante Ag4225 |
| Nom complet | adaptor-related protein complex 3, beta 1 subunit |
| Masse moléculaire calculée | 1094 aa, 121 kDa |
| Poids moléculaire observé | 140 kDa |
| Numéro d’acquisition GenBank | BC038444 |
| Symbole du gène | AP3B1 |
| Identification du gène (NCBI) | 8546 |
| Conjugaison | Non conjugué |
| Forme | Liquide |
| Méthode de purification | Purification par affinité contre l'antigène |
| Tampon de stockage | PBS only |
| Conditions de stockage | Store at -80°C. 20ul contiennent 0,1% de BSA. |
Informations générales
AP3B1 is the 140-kDa β3A subunit of the adaptor-related protein complex-3 (AP-3), a ubiquitous heterotetrameric complex that is localized to the trans-Golgi network and endosomes and is involved in protein trafficking to lysosomes or specialized endosomal-lysosomal organelles (PMID: 9182526; 9545220). This complex is composed of two larger subunits (δ and β3A or β3B), a medium subunit (μ3A or μ3B), and a small subunit (σ3A or σ3B). The absence of the β3A subunit (AP3B1) results in the loss of stability of AP3 and leads to degradation of μ3A, to which β3A is directly bound, while the other subunits are variably affected (PMID: 16507770). AP3B1 contains three main domains: the N-terminal head domain, the hinge, and the C-terminal ear domain. It has been reported as a target of IP(7)-mediated pyrophosphorylation (PMID: 19934039). Defects in AP3B1 are the cause of Hermansky-Pudlak syndrome type 2 (HPS2) (PMID: 10024875; 16507770).









