MEOX2 Antikörper

Produktnummer ABIN2460538

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch MEOX2 in WB und ELISA. Es zeigt Reaktivität gegenüber Proben von 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