TWIST1 Antikörper

Produktnummer ABIN2461623

Dieses Anti-TWIST1-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von TWIST1 in WB und ELISA. Geeignet für Human, Maus, Ratte, Zebrafisch (Danio rerio) und Hund.

Kurzübersicht für TWIST1 Antikörper (ABIN2461623)

Target: TWIST1 (Twist Homolog 1 (Drosophila) (TWIST1))

Reaktivität: Human, Maus, Ratte, Zebrafisch (Danio rerio), Hund

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser TWIST1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Produktdetails anti-TWIST1 Antikörper

Aufreinigung: Antibody is purified by protein A chromatography method.

Immunogen: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human TWIST1.

Anwendungsinformationen

Applikationshinweise: TWIST1 antibody can be used for detection of TWIST1 by ELISA at 1:1562500. TWIST1 antibody can be used for detection of TWIST1 by western blot at 2.5 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Lyophilized

Rekonstitution: Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Konzentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Handhabung: As with any antibody avoid repeat freeze-thaw cycles.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: For short periods of storage (days) store at 4 °C. For longer periods of storage, store TWIST1 antibody at -20 °C.

Details zu TWIST1

Target: TWIST1 (Twist Homolog 1 (Drosophila) (TWIST1))

Andere Bezeichnung: TWIST1

Hintergrund: Basic helix-loop-helix (bHLH) transcription factors have been implicated in cell lineage determination and differentiation.TWIST1 is a bHLH transcription factor and shares similarity with another bHLH transcription factor, Dermo1. The strongest expression of this mRNA is in placental tissue, in adults, mesodermally derived tissues express this mRNA preferentially. Mutations in this gene have been found in patients with Saethre-Chotzen syndrome.

Molekulargewicht: 21 kDa

Gen-ID: 7291

NCBI Accession: NP_000465

UniProt: Q15672

Pathways: p53 Signalweg, Proton Transport, Tube Formation, Negative Regulation of Transporter Activity