TCF25 anticorps (full length)

N° du produit ABIN7879167

L’anticorps anti-TCF25 Monoclonal Souris est utilisé pour la détection de TCF25 dans des échantillons de Humain. Il a été validé pour WB et FACS.

Aperçu rapide pour TCF25 anticorps (full length) (ABIN7879167)

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), Flow Cytometry (FACS)

Classe de qualité: Carrier-free

Clone: PCRP-TCF25-1A11

Détail du produit anti-TCF25 anticorps

Épitope: full length

Fonction: TCF-25 Antibody / Transcription factor 25 (azide and preservative free)

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: IgG2a

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: 1 mg/mL

Buffer: 1 mg/mL in 1X PBS, BSA free, sodium azide free

Agent conservateur: Azide free

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