FOXI1 Antikörper

Produktnummer ABIN2458351

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch FOXI1 in WB und ELISA. Er zeigt eine Reaktivität gegenüber Human, Maus und Ratte.

Kurzübersicht für FOXI1 Antikörper (ABIN2458351)

Target: FOXI1 (Forkhead Box I1 (FOXI1))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser FOXI1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Produktdetails anti-FOXI1 Antikörper

Aufreinigung: Antibody is purified by peptide affinity chromatography method.

Immunogen: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human FOXI1.

Anwendungsinformationen

Applikationshinweise: FOXI1 antibody can be used for detection of FOXI1 by ELISA at 1:62500. FOXI1 antibody can be used for detection of FOXI1 by western blot at 1 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 50 ?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 FOXI1 antibody at -20 °C.

Details zu FOXI1

Target: FOXI1 (Forkhead Box I1 (FOXI1))

Andere Bezeichnung: FOXI1

Hintergrund: FOXI1 belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. FOXI1 may plays an important role in the development of the cochlea and vestibulum, as well as embryogenesis.This gene belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. The specific function of this gene has not yet been determined, however, it is possible that this gene plays an important role in the development of the cochlea and vestibulum, as well as embryogenesis. Mutations in this gene may be associated with the common cavity phenotype. Two transcript variants encoding different isoforms have been found for this gene.

Molekulargewicht: 41 kDa

Gen-ID: 2299

NCBI Accession: NP_036320

UniProt: Q12951