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SOX8 anticorps

SOX8 Reactivité: Humain, Souris, Rat WB, ELISA Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN2426907
  • Antigène Voir toutes SOX8 Anticorps
    SOX8 (SRY (Sex Determining Region Y)-Box 8 (SOX8))
    Reactivité
    • 28
    • 19
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    Humain, Souris, Rat
    Hôte
    • 38
    • 4
    • 1
    Lapin
    Clonalité
    • 40
    • 3
    Polyclonal
    Conjugué
    • 14
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp SOX8 est non-conjugé
    Application
    • 32
    • 18
    • 13
    • 13
    • 4
    • 3
    • 2
    • 2
    Western Blotting (WB), ELISA
    Purification
    Antigen affinity purification
    Immunogène
    Synthetic peptide of human SOX8
    Isotype
    IgG
    Top Product
    Discover our top product SOX8 Anticorps primaire
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Conseil sur la manipulation
    Avoid freeze / thaw cycles.
    Stock
    -20 °C/-80 °C
    Stockage commentaire
    Store at -20°C (regular) and -80°C (long term).
  • Antigène
    SOX8 (SRY (Sex Determining Region Y)-Box 8 (SOX8))
    Autre désignation
    SOX8 (SOX8 Produits)
    Synonymes
    anticorps SRY-box 8, anticorps SRY box 8, anticorps SRY-box 8 L homeolog, anticorps SRY (sex determining region Y)-box 8, anticorps SOX8, anticorps Sox8, anticorps sox8.L
    Sujet
    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).
    Poids moléculaire
    Calculated MW: 47 kDa
    Pathways
    Regulation of Muscle Cell Differentiation, Tube Formation, Skeletal Muscle Fiber Development
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