Telefon:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@antikoerper-online.de

VPS13B Antikörper

VPS13B Reaktivität: Maus, Ratte IF, IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7076176
  • Target Alle VPS13B Produkte
    VPS13B (Vacuolar Protein Sorting 13 Homolog B (Yeast) (VPS13B))
    Reaktivität
    • 6
    • 5
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    Maus, Ratte
    Wirt
    • 10
    • 1
    Kaninchen
    Klonalität
    • 10
    • 1
    Polyklonal
    Konjugat
    • 7
    • 2
    • 1
    • 1
    Dieser VPS13B Antikörper ist unkonjugiert
    Applikation
    • 7
    • 5
    • 2
    • 1
    • 1
    • 1
    Immunofluorescence (IF), Immunohistochemistry (IHC)
    Kreuzreaktivität
    Ratte
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant protein corresponding to Mouse VPS13B/CHS1
  • Applikationshinweise
    IHC/IF (M,R) 1:1000-1:2000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Buffer
    PBS, pH 7.4, 0.02 % sodium azide
    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
  • Target
    VPS13B (Vacuolar Protein Sorting 13 Homolog B (Yeast) (VPS13B))
    Andere Bezeichnung
    VPS13B/CHS1 (VPS13B Produkte)
    Synonyme
    1810042B05Rik antikoerper, 2310042E16Rik antikoerper, 4732488H20 antikoerper, C330002D13Rik antikoerper, C87206 antikoerper, Coh1 antikoerper, D230005K13 antikoerper, mKIAA0532 antikoerper, mKIAA5032 antikoerper, CHS1 antikoerper, COH1 antikoerper, Cohh1 antikoerper, vacuolar protein sorting 13 homolog B antikoerper, vacuolar protein sorting 13B antikoerper, VPS13B antikoerper, Vps13b antikoerper
    Hintergrund
    This gene encodes a potential transmembrane protein that may function in vesicle-mediated transport and sorting of proteins within the cell. This protein may play a role in the development and the function of the eye, hematological system, and central nervous system. Mutations in this gene have been associated with Cohen syndrome. Multiple splice variants encoding distinct isoforms have been identified for this gene.
    Gen-ID
    666173
    NCBI Accession
    NP_796125
    UniProt
    Q80TY5
Sie sind hier:
Kundenservice