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

TMEM176A Antikörper

TMEM176A Reaktivität: Ratte IF, IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7075995
  • Target Alle TMEM176A Produkte
    TMEM176A (Transmembrane Protein 176A (TMEM176A))
    Reaktivität
    • 15
    • 15
    • 7
    • 1
    Ratte
    Wirt
    • 21
    • 1
    Kaninchen
    Klonalität
    • 21
    • 1
    Polyklonal
    Konjugat
    • 8
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser TMEM176A Antikörper ist unkonjugiert
    Applikation
    • 22
    • 13
    • 13
    • 5
    • 4
    • 3
    • 1
    • 1
    Immunofluorescence (IF), Immunohistochemistry (IHC)
    Kreuzreaktivität
    Ratte
    Aufreinigung
    Affinity purification
    Immunogen
    KLH conjugated Synthetic peptide corresponding to Mouse TMEM176A
  • Applikationshinweise
    IHC/IF (R) 1:500-1:1000
    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
    TMEM176A (Transmembrane Protein 176A (TMEM176A))
    Andere Bezeichnung
    TMEM176A (TMEM176A Produkte)
    Synonyme
    GS188 antikoerper, HCA112 antikoerper, 0610011I04Rik antikoerper, AU040201 antikoerper, AU041743 antikoerper, Keg2 antikoerper, 0610011i04rik antikoerper, RGD1310725 antikoerper, CL1 antikoerper, transmembrane protein 176A antikoerper, TMEM176A antikoerper, Tmem176a antikoerper
    Hintergrund
    TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5 % of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance.
    Gen-ID
    66058
    UniProt
    Q9DCS1
Sie sind hier: