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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.
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蛋白别名: CD349; CD349 antigen; Frizzled 3; frizzled 9, seven transmembrane spanning receptor; frizzled family receptor 9; frizzled homolog 9; Frizzled-9; Frizzled3; Frizzled9; Fz-9; FzE6; hFz9
基因别名: CD349; FZD3; FZD9
UniProt ID: (Human) O00144
Entrez Gene ID: (Human) 8326