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Antibody detects endogenous levels of total FZD9.
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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: CD349; CD349 antigen; Frizzled 3; frizzled 9, seven transmembrane spanning receptor; frizzled family receptor 9; frizzled homolog 9; Frizzled-3; Frizzled-9; Frizzled3; Frizzled9; Fz-9; FzE6; hFz9; mFz3
基因别名: CD349; FZD3; FZD9; mfz9
UniProt ID: (Human) O00144, (Mouse) Q9R216
Entrez Gene ID: (Human) 8326, (Mouse) 14371