|Immunohistochemistry (Paraffin) (IHC (P))||14 µg/ml|
|Tested Species reactivity||Human|
|Host / Isotype||Rabbit / IgG|
|Immunogen||Synthetic 14 amino acid peptide from N-terminal extracellular domain of human FZD9 / Frizzled 9.|
|Purification||Antigen affinity chromatography|
|Contains||< 0.1% sodium azide|
|Storage conditions||Maintain refrigerated at 2-8°C for up to 1 month. For long term storage store at -20°C|
Percent identity with other species by BLAST analysis: Human, Gibbon, Dog, Rabbit (100%) Mouse, Rat, Hamster, Bovine (93%) Panda (86%).
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: CD349; CD349 antigen; Frizzled 9; frizzled 9, seven transmembrane spanning receptor; Frizzled family receptor 9; Frizzled homolog 9; Frizzled homolog fzd3; Frizzled-9; Fz-9; Fz9; FZD9; FzE6; HFz9
Gene Aliases: CD349; FZD3; FZD9
UniProt ID: (Human) O00144
Entrez Gene ID: (Human) 8326
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