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HPS1 anticorps

Cet anticorps anti-HPS1 est un anticorps Lapin Polyclonal détectant HPS1 dans WB, IHC, ELISA et IF. Adapté pour Humain, Souris et Rat.
N° du produit ABIN7114965

Aperçu rapide pour HPS1 anticorps (ABIN7114965)

Antigène

Voir toutes HPS1 Anticorps
HPS1 (Hermansky-Pudlak Syndrome 1 (HPS1))

Reactivité

Humain, Souris, Rat

Hôte

  • 12
  • 2
Lapin

Clonalité

  • 12
  • 2
Polyclonal

Conjugué

  • 7
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp HPS1 est non-conjugé

Application

  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF)
  • Fonction

    HPS1 antibody

    Purification

    Immunogen affinity purified

    Pureté

    ≥95 % as determined by SDS-PAGE

    Immunogène

    Hermansky-Pudlak syndrome 1

    Isotype

    IgG
  • Indications d'application

    WB: 1:500 - 1:2000, IHC: 1:50 - 1:100, IF: 1:50 - 1:100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Conseil sur la manipulation

    Avoid repeated freeze / thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

    -20°C for 12 months

    Date de péremption

    12 months
  • Antigène

    HPS1 (Hermansky-Pudlak Syndrome 1 (HPS1))

    Autre désignation

    HPS1

    Sujet

    Synonyms: BLOC-3 complex member HPS1|Hermansky-Pudlak syndrome 1 protein|HPS1|HPS

    Background: This gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. The encoded protein is a component of three different protein complexes termed biogenesis of lysosome-related organelles complex (BLOC)-3, BLOC4, and BLOC5. Mutations in this gene are associated with Hermansky-Pudlak syndrome type 1. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on chromosome 22.

    Poids moléculaire

    70-79 kDa

    ID gène

    3257

    UniProt

    Q92902
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