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SHOX2 anticorps

SHOX2 Reactivité: Humain, Rat, Souris WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7264337
  • Antigène Voir toutes SHOX2 Anticorps
    SHOX2 (Short Stature Homeobox 2 (SHOX2))
    Reactivité
    • 17
    • 9
    • 7
    • 5
    • 5
    • 5
    • 4
    • 3
    • 2
    • 2
    • 2
    Humain, Rat, Souris
    Hôte
    • 10
    • 7
    Lapin
    Clonalité
    • 13
    • 4
    Polyclonal
    Conjugué
    • 17
    Cet anticorp SHOX2 est non-conjugé
    Application
    • 14
    • 8
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human SHOX2 (NP_003021.3).
    Isotype
    IgG
    Top Product
    Discover our top product SHOX2 Anticorps primaire
  • Indications d'application
    WB 1:500-1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    SHOX2 (Short Stature Homeobox 2 (SHOX2))
    Autre désignation
    SHOX2 (SHOX2 Produits)
    Synonymes
    anticorps SHOX2, anticorps og12, anticorps shot, anticorps og12x, anticorps ogi2x, anticorps OG12, anticorps OG12X, anticorps SHOT, anticorps 6330543G17Rik, anticorps Og12x, anticorps Prx3, anticorps zgc:65884, anticorps zgc:77344, anticorps short stature homeobox 2, anticorps SHOX2, anticorps shox2, anticorps Shox2
    Sujet
    This gene is a member of the homeobox family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Homeobox genes have been characterized extensively as transcriptional regulators involved in pattern formation in both invertebrate and vertebrate species. Several human genetic disorders are caused by aberrations in human homeobox genes. This locus represents a pseudoautosomal homeobox gene that is thought to be responsible for idiopathic short stature, and it is implicated in the short stature phenotype of Turner syndrome patients. This gene is considered to be a candidate gene for Cornelia de Lange syndrome. Alternative splicing results in multiple transcript variants.
    Poids moléculaire

    Observed_MW: 30 kDa

    Calculated_MW: 33 kDa/34 kDa/37 kDa

    ID gène
    6474
    UniProt
    O60902
    Pathways
    Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
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