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SHOX2 Antikörper

Dieses Anti-SHOX2-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von SHOX2 in WB. Geeignet für Human, Ratte und Maus.
Produktnummer ABIN7264337

Kurzübersicht für SHOX2 Antikörper (ABIN7264337)

Target

Alle SHOX2 Antikörper anzeigen
SHOX2 (Short Stature Homeobox 2 (SHOX2))

Reaktivität

  • 18
  • 9
  • 7
  • 5
  • 5
  • 5
  • 4
  • 3
  • 2
  • 2
  • 2
Human, Ratte, Maus

Wirt

  • 11
  • 7
Kaninchen

Klonalität

  • 14
  • 4
Polyklonal

Konjugat

  • 18
Dieser SHOX2 Antikörper ist unkonjugiert

Applikation

  • 14
  • 9
  • 2
  • 2
  • 1
Western Blotting (WB)
  • Produktmerkmale

    Polyclonal Antibody

    Aufreinigung

    Affinity purification

    Immunogen

    Recombinant fusion protein of human SHOX2 (NP_003021.3).

    Isotyp

    IgG
  • 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

    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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