T-Box 19 anticorps (AA 200-400)

N° du produit ABIN6945138

Cet anticorps Lapin Monoclonal détecte spécifiquement T-Box 19 dans WB, IHC (p), IP, FACS et IF (cc). Il présente une réactivité avec des échantillons de Humain.

Aperçu rapide pour T-Box 19 anticorps (AA 200-400) (ABIN6945138)

Antigène: T-Box 19 (TBX19)

Reactivité: Humain

Hôte: Lapin

Clonalité: Monoclonal

Conjugué: Cet anticorp T-Box 19 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunoprecipitation (IP), Flow Cytometry (FACS), Immunofluorescence (Cultured Cells) (IF (cc))

Clone: 1F11

Détail du produit anti-T-Box 19 anticorps

Épitope: AA 200-400

Fonction: TBXT Recombinant Antibody

Réactivité croisée: Humain, Souris

Purification: Purified by Protein A.

Immunogène: Recombinant protein within human TBXT aa 200-400.

Isotype: IgG

Information d'application

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

Stockage

Format: Liquid

Concentration: Lot specific

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

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

Détails sur T-Box 19

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