Frizzled-9 Polyclonal Antibody, 20ul[BT-AP03370] Hepatocytes It is mainly expressed in

It is mainly expressed in skeletal and cardiac muscles and may be involved in differentiation and migration processes during myogenesis

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Ephrin receptors and their ligands

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

ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core

Frizzled-9 Polyclonal Antibody, 20ul[BT-AP03370] Hepatocytes It is mainly expressed inMembers 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.