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SHOX2 Antikörper

SHOX2 Reaktivität: Human, Ratte, Maus WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7264337
  • Target Alle SHOX2 Antikörper anzeigen
    SHOX2 (Short Stature Homeobox 2 (SHOX2))
    Reaktivität
    • 17
    • 9
    • 7
    • 5
    • 5
    • 5
    • 4
    • 3
    • 2
    • 2
    • 2
    Human, Ratte, Maus
    Wirt
    • 10
    • 7
    Kaninchen
    Klonalität
    • 13
    • 4
    Polyklonal
    Konjugat
    • 17
    Dieser SHOX2 Antikörper ist unkonjugiert
    Applikation
    • 14
    • 8
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant fusion protein of human SHOX2 (NP_003021.3).
    Isotyp
    IgG
    Top Product
    Discover our top product SHOX2 Primärantikörper
  • Applikationshinweise
    WB 1:500-1:2000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    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
    SHOX2 (Short Stature Homeobox 2 (SHOX2))
    Andere Bezeichnung
    SHOX2 (SHOX2 Produkte)
    Synonyme
    SHOX2 antikoerper, og12 antikoerper, shot antikoerper, og12x antikoerper, ogi2x antikoerper, OG12 antikoerper, OG12X antikoerper, SHOT antikoerper, 6330543G17Rik antikoerper, Og12x antikoerper, Prx3 antikoerper, zgc:65884 antikoerper, zgc:77344 antikoerper, short stature homeobox 2 antikoerper, SHOX2 antikoerper, shox2 antikoerper, Shox2 antikoerper
    Hintergrund
    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.
    Molekulargewicht

    Observed_MW: 30 kDa

    Calculated_MW: 33 kDa/34 kDa/37 kDa

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