TCF25 Antikörper (full length)

Produktnummer ABIN7879165

Der Maus Monoklonal anti-TCF25 Antikörper (Klon PCRP-TCF25-1F12) (ABIN7879165) detektiert spezifisch TCF25 in WB. Dieser Antikörper reagiert spezifisch mit Proben aus Human.

Kurzübersicht für TCF25 Antikörper (full length) (ABIN7879165)

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

Reaktivität: Human

Wirt: Maus

Klonalität: Monoklonal

Konjugat: Dieser TCF25 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Güteklasse: Carrier-free

Klon: PCRP-TCF25-1F12

Produktdetails anti-TCF25 Antikörper

Bindungsspezifität: full length

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

Aufreinigung: Protein A/G affinity

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

Isotyp: IgG1

Anwendungsinformationen

Applikationshinweise: Optimal dilution of the TCF-25 antibody should be determined by the researcher.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

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

Konservierungsmittel: Azide free

Lagerung: -20 °C

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

Details zu TCF25

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

Andere Bezeichnung: TCF-25

Hintergrund: 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