MEOX2 Antikörper

Produktnummer ABIN2460538

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch MEOX2 in WB und ELISA. Er zeigt eine Reaktivität gegenüber Human, Ratte, Maus und Hund.

Kurzübersicht für MEOX2 Antikörper (ABIN2460538)

Target: MEOX2 (Mesenchyme Homeobox 2 (MEOX2))

Reaktivität: Human, Ratte, Maus, Hund

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser MEOX2 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Produktdetails anti-MEOX2 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 MEOX2.

Anwendungsinformationen

Applikationshinweise: MEOX2 antibody can be used for detection of MEOX2 by ELISA at 1:312500. MEOX2 antibody can be used for detection of MEOX2 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 MEOX2 antibody at -20 °C.

Details zu MEOX2

Target: MEOX2 (Mesenchyme Homeobox 2 (MEOX2))

Andere Bezeichnung: MEOX2

Hintergrund: MEOX2 is a member of a subfamily of non-clustered, diverged, antennapedia-like homeobox-containing genes. MEOX2 may play a role in the regulation of vertebrate limb myogenesis. Mutations in the related mouse protein may be associated with craniofacial and/or skeletal abnormalities, in addition to neurovascular dysfunction observed in Alzheimer's disease.This gene encodes a member of a subfamily of non-clustered, diverged, antennapedia-like homeobox-containing genes. The encoded protein may play a role in the regulation of vertebrate limb myogenesis. Mutations in the related mouse protein may be associated with craniofacial and/or skeletal abnormalities, in addition to neurovascular dysfunction observed in Alzheimer's disease.

Molekulargewicht: 33 kDa

Gen-ID: 4223

NCBI Accession: NP_005915

UniProt: P50222