TCF25 anticorps (full length)

N° du produit ABIN7879166

Cet anticorps Souris Monoclonal détecte spécifiquement TCF25 dans WB. Il présente une réactivité avec des échantillons de Humain.

Aperçu rapide pour TCF25 anticorps (full length) (ABIN7879166)

Antigène: TCF25 (Transcription Factor 25 (Basic Helix-Loop-Helix) (TCF25))

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp TCF25 est non-conjugé

Application: Western Blotting (WB)

Clone: PCRP-TCF25-1F12

Détail du produit anti-TCF25 anticorps

Épitope: full length

Fonction: TCF-25 Antibody / Transcription factor 25

Purification: Protein A/G affinity

Immunogène: Recombinant full-length human Transcription factor 25 protein was used as the immunogen for the TCF-25 antibody.

Isotype: IgG1

Information d'application

Indications d'application: Optimal dilution of the TCF-25 antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.2 mg/mL

Buffer: 0.2 mg/mL in 1X PBS with 0.1 mg/mL BSA (US sourced), 0.05 % sodium azide

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: Aliquot the TCF-25 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Détails sur TCF25

Antigène: TCF25 (Transcription Factor 25 (Basic Helix-Loop-Helix) (TCF25))

Autre désignation: TCF-25

Sujet: Nulp1 (nuclear localized protein 1), also known as TCF25 (transcription factor 25 (basic helix-loop-helix)), Hulp1 or FKSG26, is a 676 amino acid protein that plays a role in cell death. A member of the TCF25 family, Nulp1 utilizes its C-terminus to mediate transcriptional repression of SRF in vitro, and interacts with XIAP. Nulp1 localizes primarily to the nucleus but is also found in cytosol. Widely expressed, Nulp1 is found at high levels in embryonic brain and adult heart. The gene encoding Nulp1 maps to human chromosome 16q24.3, which encodes over 900 genes and comprises nearly 3 % of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn s disease, which is a gastrointestinal inflammatory condition.

UniProt: Q9BQ70