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BUD31 Antikörper

Der Kaninchen Polyklonal Anti-BUD31-Antikörper wurde für WB, ELISA und IHC validiert. Er ist geeignet, BUD31 in Proben von Human, Ratte und Maus zu detektieren.
Produktnummer ABIN7246052

Kurzübersicht für BUD31 Antikörper (ABIN7246052)

Target

Alle BUD31 Antikörper anzeigen
BUD31 (BUD31 Homolog (BUD31))

Reaktivität

  • 46
  • 29
  • 21
  • 5
  • 5
  • 5
  • 4
  • 4
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Ratte, Maus

Wirt

  • 42
  • 4
Kaninchen

Klonalität

  • 43
  • 3
Polyklonal

Konjugat

  • 28
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
Dieser BUD31 Antikörper ist unkonjugiert

Applikation

  • 25
  • 17
  • 11
  • 7
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Produktmerkmale

    Polyclonal Antibody

    Aufreinigung

    Antigen affinity purification

    Immunogen

    Full length fusion protein

    Isotyp

    IgG
  • Applikationshinweise

    WB 1:1000-1:5000, IHC 1:50-1:300, ELISA 1:5000-1:10000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1.5 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    BUD31 (BUD31 Homolog (BUD31))

    Andere Bezeichnung

    BUD31

    Hintergrund

    BUD31 (Protein G10 homolog, EDG-2) is a 144 amino acid protein encoded by the human gene BUD31. BUD31 is a nuclear protein that belongs to the BUD31 (G10) family. BUD31 is found on chromosome 7 which is about 158 milllion bases long, encodes over 1,000 genes and makes up about 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 long (q) arm of human 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. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.

    Molekulargewicht

    Observed_MW: Refer to figures

    Calculated_MW: 17 kDa

    UniProt

    P41223
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