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HPS1 Antikörper

HPS1 Reaktivität: Human, Maus, Ratte IHC, IF Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7262497
  • Target Alle HPS1 Antikörper anzeigen
    HPS1 (Hermansky-Pudlak Syndrome 1 (HPS1))
    Reaktivität
    Human, Maus, Ratte
    Wirt
    • 12
    • 1
    Kaninchen
    Klonalität
    • 12
    • 1
    Polyklonal
    Konjugat
    • 6
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser HPS1 Antikörper ist unkonjugiert
    Applikation
    • 4
    • 4
    • 3
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC), Immunofluorescence (IF)
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant fusion protein of human HPS1 (NP_872577.1).
    Isotyp
    IgG
  • Applikationshinweise
    IHC 1:50-1:100 IF 1:50-1:100
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    HPS1 (Hermansky-Pudlak Syndrome 1 (HPS1))
    Andere Bezeichnung
    HPS1 (HPS1 Produkte)
    Synonyme
    HPS antikoerper, HPS1 antikoerper, MGC123240 antikoerper, im:7143944 antikoerper, zgc:123240 antikoerper, 6030422N11Rik antikoerper, BB405864 antikoerper, Hps antikoerper, ep antikoerper, HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 antikoerper, Hermansky-Pudlak syndrome 1 antikoerper, HPS1 antikoerper, hps1 antikoerper, Hps1 antikoerper
    Hintergrund
    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.
    Gen-ID
    3257
    UniProt
    Q92902
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