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SHOX2 anticorps

Cet anticorps anti-SHOX2 est un anticorps Lapin Polyclonal détectant SHOX2 dans WB. Adapté pour Humain, Rat et Souris.
N° du produit ABIN7264337

Aperçu rapide pour SHOX2 anticorps (ABIN7264337)

Antigène

Voir toutes SHOX2 Anticorps
SHOX2 (Short Stature Homeobox 2 (SHOX2))

Reactivité

  • 20
  • 9
  • 7
  • 5
  • 5
  • 5
  • 4
  • 3
  • 2
  • 2
  • 2
Humain, Rat, Souris

Hôte

  • 10
  • 10
Lapin

Clonalité

  • 13
  • 7
Polyclonal

Conjugué

  • 17
  • 1
  • 1
  • 1
Cet anticorp SHOX2 est non-conjugé

Application

  • 17
  • 8
  • 3
  • 3
  • 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
  • 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

    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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