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SATB2 anticorps

Cet anticorps anti-SATB2 Polyclonal Lapin (ABIN7882211) détecte spécifiquement SATB2 dans WB. L’anticorps est réactif avec des échantillons de Humain.
N° du produit ABIN7882211
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour SATB2 anticorps (ABIN7882211)

Antigène

Voir toutes SATB2 Anticorps
SATB2 (SATB Homeobox 2 (SATB2))

Reactivité

  • 141
  • 46
  • 40
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 104
  • 37
Lapin

Clonalité

  • 96
  • 45
Polyclonal

Conjugué

  • 93
  • 6
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp SATB2 est non-conjugé

Application

  • 80
  • 62
  • 30
  • 26
  • 16
  • 15
  • 14
  • 13
  • 13
  • 8
  • 3
  • 3
  • 2
  • 1
Western Blotting (WB)
  • Fonction

    SATB2 Antibody / Special AT-rich sequence-binding protein 2

    Séquence

    ERMQHVVQLP PEPVQVLHRQ Q

    Purification

    Antigen affinity purified

    Immunogène

    Amino acids ERMQHVVQLPPEPVQVLHRQQ were used as the immunogen for the SATB2 antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the SATB2 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Stock

    4 °C,-20 °C

    Stockage commentaire

    After reconstitution, the SATB2 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Antigène

    SATB2 (SATB Homeobox 2 (SATB2))

    Autre désignation

    SATB2

    Sujet

    Special AT-rich sequence-binding protein 2 (SATB2) also known as DNA-binding protein SATB2 is a protein that in humans is encoded by the SATB2 gene. This gene encodes a DNA binding protein that specifically binds nuclear matrix attachment regions. The encoded protein is involved in transcription regulation and chromatin remodeling. Defects in this gene are associated with isolated cleft palate and cognitive disability. Alternate splicing results in multiple transcript variants that encode the same protein.

    UniProt

    Q9UPW6
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