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SOX8 Antikörper

SOX8 Reaktivität: Human, Maus, Ratte WB, ELISA Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN2426907
  • Target Alle SOX8 Antikörper anzeigen
    SOX8 (SRY (Sex Determining Region Y)-Box 8 (SOX8))
    Reaktivität
    • 28
    • 19
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Maus, Ratte
    Wirt
    • 38
    • 4
    • 1
    Kaninchen
    Klonalität
    • 40
    • 3
    Polyklonal
    Konjugat
    • 14
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser SOX8 Antikörper ist unkonjugiert
    Applikation
    • 32
    • 18
    • 13
    • 13
    • 4
    • 3
    • 2
    • 2
    Western Blotting (WB), ELISA
    Aufreinigung
    Antigen affinity purification
    Immunogen
    Synthetic peptide of human SOX8
    Isotyp
    IgG
    Top Product
    Discover our top product SOX8 Primärantikörper
  • Applikationshinweise
    Optimal working dilution should be determined by the investigator.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Handhabung
    Avoid freeze / thaw cycles.
    Lagerung
    -20 °C/-80 °C
    Informationen zur Lagerung
    Store at -20°C (regular) and -80°C (long term).
  • Target
    SOX8 (SRY (Sex Determining Region Y)-Box 8 (SOX8))
    Andere Bezeichnung
    SOX8 (SOX8 Produkte)
    Synonyme
    SRY-box 8 antikoerper, SRY box 8 antikoerper, SRY-box 8 L homeolog antikoerper, SRY (sex determining region Y)-box 8 antikoerper, SOX8 antikoerper, Sox8 antikoerper, sox8.L antikoerper
    Hintergrund
    This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional activator after forming a protein complex with other proteins. This protein may be involved in brain development and function. Haploinsufficiency for this protein may contribute to the mental retardation found in haemoglobin H-related mental retardation (ART-16 syndrome).
    Molekulargewicht
    Calculated MW: 47 kDa
    Pathways
    Regulation of Muscle Cell Differentiation, Tube Formation, Skeletal Muscle Fiber Development
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