Frizzled-9 Polyclonal Antibody, 20ul[BT-AP03370] Hepatocytes Unleash your potential with bold

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The EPH receptor B4 encoded by EPHB4 binds to ephrin-B2 and plays an essential role in vascular development

which is a congenital disorder of spinal segmentation

Defects in this gene are a cause of zonular pulverulent cataract type 3 (CZP3)

Frizzled-9 Polyclonal Antibody, 20ul[BT-AP03370] Hepatocytes Unleash your potential with boldMembers of the frizzled gene family encode 7 transmembrane domain proteins that are receptors for Wnt signaling proteins. The FZD9 gene (frizzled class receptor 9) 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.