HOXD1 Antikörper

Produktnummer ABIN2457968

Der Kaninchen-Polyklonal Anti-HOXD1-Antikörper wurde für WB und ELISA validiert. Er ist geeignet zum Nachweis von HOXD1 in Proben aus Human, Maus und Ratte. }

Kurzübersicht für HOXD1 Antikörper (ABIN2457968)

Target: HOXD1 (Homeobox D1 (HOXD1))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser HOXD1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Produktdetails anti-HOXD1 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 HOXD1.

Anwendungsinformationen

Applikationshinweise: HOXD1 antibody can be used for detection of HOXD1 by ELISA at 1:312500. HOXD1 antibody can be used for detection of HOXD1 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 HOXD1 antibody at -20 °C.

Details zu HOXD1

Target: HOXD1 (Homeobox D1 (HOXD1))

Andere Bezeichnung: HOXD1

Hintergrund: HOXD1 is a protein with a homeobox DNA-binding domain, and it belongs to the Antp homeobox family. This nuclear protein functions as a sequence-specific transcription factor that is involved in differentiation and limb development. Mutations in this gene have been associated with severe developmental defects on the anterior-posterior (a-p) limb axis.This gene is a member of the Antp homeobox family and encodes a protein with a homeobox DNA-binding domain. This nuclear protein functions as a sequence-specific transcription factor that is involved in differentiation and limb development. Mutations in this gene have been associated with severe developmental defects on the anterior-posterior (a-p) limb axis. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

Molekulargewicht: 34 kDa

Gen-ID: 3231

NCBI Accession: NP_078777

UniProt: Q9GZZ0