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Invitrogen™ FZD9 Recombinant Rabbit Monoclonal Antibody (23GB5475), Invitrogen™

Description
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.
Specifications
Specifications
| Antigen | FZD9 |
| Applications | Western Blot, Immunocytochemistry |
| Classification | Recombinant Monoclonal |
| Clone | 23GB5475 |
| Concentration | 1.2 mg/mL |
| Conjugate | Unconjugated |
| Formulation | PBS with 50% glycerol and 0.02% sodium azide; pH 7.4 |
| Gene | FZD9 |
| Gene Accession No. | O00144 |
| Gene Alias | CD349; CD349 antigen; Frizzled 3; frizzled 9; frizzled 9, seven transmembrane spanning receptor; frizzled class receptor 9; frizzled family receptor 9; frizzled homolog 9; frizzled homolog 9 (Drosophila); Frizzled3; Frizzled-3; Frizzled9; frizzled-9; Frizzled-like protein 9; fz-9; FZD3; FZD9; FzE6; hFz9; mFz3; mfz9; rFz9 |
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