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RNF148 Antikörper

RNF148 Reaktivität: Human ELISA, IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7239431
  • Target Alle RNF148 Produkte
    RNF148 (Ring Finger Protein 148 (RNF148))
    Reaktivität
    • 32
    • 1
    • 1
    • 1
    Human
    Wirt
    • 29
    • 3
    Kaninchen
    Klonalität
    • 29
    • 3
    Polyklonal
    Konjugat
    • 12
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser RNF148 Antikörper ist unkonjugiert
    Applikation
    • 20
    • 20
    • 2
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Affinity purification
    Immunogen
    Synthetic peptide of human RNF148
    Isotyp
    IgG
  • Applikationshinweise
    IHC 1:50-1:200
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    0.8 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    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
    RNF148 (Ring Finger Protein 148 (RNF148))
    Andere Bezeichnung
    RNF148 (RNF148 Produkte)
    Synonyme
    4933432M07Rik antikoerper, Greul3 antikoerper, ring finger protein 148 antikoerper, Rnf148 antikoerper, RNF148 antikoerper
    Hintergrund
    RNF148 (RING finger protein 148) is a 305 amino acid single-pass membrane protein that contains one PA (protease associated) domain and a single RING-type zinc finger. RNF148 is encoded by a gene that 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.
    NCBI Accession
    NP_932351
    UniProt
    Q8N7C7
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