FZD9 Antikörper (AA 542-591)

Produktnummer ABIN1535616

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch FZD9 in WB, ELISA und IF. Es zeigt Reaktivität gegenüber Proben von Human, Maus und Affe.

Kurzübersicht für FZD9 Antikörper (AA 542-591) (ABIN1535616)

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

Reaktivität: Human, Maus, Affe

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser FZD9 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA, Immunofluorescence (IF)

Produktdetails anti-FZD9 Antikörper

Bindungsspezifität: AA 542-591

Verwendungszweck: Frizzled-9 Antibody

Spezifität: Frizzled-9 Polyclonal Antibody detects endogenous levels of Frizzled-9 protein.

Aufreinigung: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Reinheit: > 95 %

Immunogen: The antiserum was produced against synthesized peptide derived from human FZD9. AA range:542-591

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500 - 1:2000. IF 1:200 - 1:1000. ELISA: 1:20000. Not yet tested in other applications.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 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: Store at -20°C/1 year

Haltbarkeit: 12 months

Details zu FZD9

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

Andere Bezeichnung: FZD9

Hintergrund:

Synonyms: FZD9; FZD3; Frizzled-9; Fz-9; hFz9; FzE6; CD antigen CD349

Background: frizzled class receptor 9(FZD9) Homo sapiens 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. [provided by RefSeq, Jul 2008],

Gene Name: FZD9

Protein Name: Frizzled-9

Molekulargewicht: 64 kDa

Gen-ID: 8326

OMIM: 601766

UniProt: O00144

Pathways: WNT Signalweg