Background:

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. Frizzled-9 is expressed predominantly in brain, testis, eye, skeletal muscle, and kidney.

Classification:

Primary antibody

Alternative names:

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

Species reactivity:

Human;Mouse;Monkey

Host:

Rabbit

Isotype:

IgG

Immunogen:

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

Concentration:

1 mg/ml

Molecular weight:

64466

Applications:

WB, IF, ELISA

Storage:

-20°C for one year

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