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T-Box 19 anticorps

Cet anticorps Lapin Monoclonal détecte spécifiquement T-Box 19 dans WB, IP, IHC (p), FACS et IF (cc). Il présente une réactivité envers Humain et Souris.
N° du produit ABIN6945138

Aperçu rapide pour T-Box 19 anticorps (ABIN6945138)

Antigène

Voir toutes T-Box 19 (TBX19) Anticorps
T-Box 19 (TBX19)

Reactivité

  • 11
  • 7
  • 7
  • 5
  • 4
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Humain, Souris

Hôte

  • 11
  • 1
Lapin

Clonalité

  • 10
  • 2
Monoclonal

Conjugué

  • 12
Cet anticorp T-Box 19 est non-conjugé

Application

  • 12
  • 5
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunoprecipitation (IP), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS), Immunofluorescence (Cultured Cells) (IF (cc))

Clone

1F11
  •  Réactivité croisée

    Humain, Souris

    Purification

    Purified by Protein A.

    Immunogène

    Recombinant protein within human TBXT aa 200-400.

    Isotype

    IgG
  • Indications d'application

    WB 1:300-5000
    FCM 1:20-100
    IHC-P 1:200-400
    IF(ICC) 1:50-200
    IP(1-2 μg)

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 1xTBS ( pH 7.4), 1 % BSA, 40 %Glycerol and 0.05 % Sodium Azide.

    Agent conservateur

    ProClin

    Précaution d'utilisation

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C for 12 months.

    Date de péremption

    12 months
  • Antigène

    T-Box 19 (TBX19)

    Autre désignation

    TBXT

    Sujet

    Synonyms: T-box transcription factor T, TBXT, Brachyury protein

    Background: TBXTis an embryonic nuclear transcription factor that binds to a specific DNA element, the palindromic T-site. It binds through a region in its N-terminus, called the T-box, and effects transcription of genes required for mesoderm formation and differentiation. The protein is localized to notochord-derived cells. Variation in this gene was associated with susceptibility to neural tube defects and chordoma. A mutation in this gene was found in a family with sacral agenesis with vertebral anomalies. Involved in the transcriptional regulation of genes required for mesoderm formation and differentiation.

    ID gène

    6862

    UniProt

    O15178
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