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OLIG2 Antikörper

OLIG2 Reaktivität: Human, Maus, Ratte, Huhn WB, ELISA, IHC, IF/ICC Wirt: Maus Monoclonal unconjugated
Produktnummer ABIN1845900
  • Target Alle OLIG2 Antikörper anzeigen
    OLIG2 (Oligodendrocyte Lineage Transcription Factor 2 (OLIG2))
    Reaktivität
    • 63
    • 41
    • 36
    • 5
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Human, Maus, Ratte, Huhn
    Wirt
    • 66
    • 10
    Maus
    Klonalität
    • 57
    • 19
    Monoklonal
    Konjugat
    • 42
    • 6
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser OLIG2 Antikörper ist unkonjugiert
    Applikation
    • 42
    • 31
    • 21
    • 14
    • 14
    • 13
    • 13
    • 9
    • 7
    • 7
    • 4
    • 4
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunofluorescence (fixed cells) (IF/ICC)
    Immunogen
    Purified recombinant fragment of human OLIG2 expressed in E. coli.
    Isotyp
    IgG1
    Top Product
    Discover our top product OLIG2 Primärantikörper
  • Applikationshinweise
    Optimal working dilution should be determined by the investigator.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Buffer
    Ascitic fluid containing 0.03 % 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
    Informationen zur Lagerung
    Aliquot and store at -20 °C. Avoid repeated freeze/thaw cycles.
  • Target
    OLIG2 (Oligodendrocyte Lineage Transcription Factor 2 (OLIG2))
    Andere Bezeichnung
    OLIG2 (OLIG2 Produkte)
    Hintergrund
    This gene encodes a basic helix-loop-helix transcription factor which is expressed in oligodendroglial tumors of the brain.The protein is an essential regulator of ventral neuroectodermal progenitor cell fate.The gene is involved in a chromosomal translocation t (14,21) (q11.2,q22) associated with T-cell acute lymphoblastic leukemia.Its chromosomal location is within a region of chromosome 21 which has been suggested to play a role in learning deficits associated with Down syndrome.Tissue specificity: Expressed in the brain, in oligodendrocytes.Strongly expressed in oligodendrogliomas, while expression is weak to moderate in astrocytomas.Expression in glioblastomas highly variable.
    Molekulargewicht
    32 kDa
    Gen-ID
    10215, 50913, 304103
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