FZD9 Antikörper (AA 27-591) (Fluoro594)

Produktnummer ABIN7991883

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch FZD9 in FACS. Es zeigt Reaktivität gegenüber Proben von Human, Maus und Ratte.

Kurzübersicht für FZD9 Antikörper (AA 27-591) (Fluoro594) (ABIN7991883)

Target: FZD9 (Frizzled Family Receptor 9 (FZD9))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser FZD9 Antikörper ist konjugiert mit Fluoro594

Applikation: Flow Cytometry (FACS)

Produktdetails anti-FZD9 Antikörper (Fluoro594)

Bindungsspezifität: AA 27-591

Verwendungszweck: Anti-Frizzled 9/FZD9 Antibody Fluoro594 Conjugated

Kreuzreaktivität (Details): No cross-reactivity with other proteins

Homologie: Human Frizzled 9,FZD9 shares 95.9%,96.1% amino acid (aa) sequence identity with mouse,rat Frizzled 9,FZD9,respectively.

Aufreinigung: Immunogen affinity purified.

Immunogen: E.coli-derived human Frizzled 9/FZD9 recombinant protein (Position: R27-L591). Human Frizzled 9/FZD9 shares 95.9% and 96.1% amino acid (aa) sequence identity with mouse and rat Frizzled 9/FZD9, respectively.

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Flow Cytometry, Optimal dilutions should be determined by end users.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Haltbarkeit: 12 months

Details zu FZD9

Target: FZD9 (Frizzled Family Receptor 9 (FZD9))

Andere Bezeichnung: FZD9

Hintergrund:

Background: Members of the 'frizzled' gene family encode 7-transmembrane domain proteins that are receptors for Wnt signaling proteins. The FZD9 gene is located within the Williams syndrome common deletion region of chromosome 7, and heterozygous deletion of the FZD9 gene may contribute to the Williams syndrome phenotype. FZD9 is expressed predominantly in brain, testis, eye, skeletal muscle, and kidney.

Gene Full Name: frizzled class receptor 9

Gen-ID: 8326

UniProt: O00144

Pathways: WNT Signalweg