synthetic peptide corresponding to the N-terminal extracellular domain of human frizzled-1, conjugated KLH. The immunizing peptide has 85% homology with the rat and mouse gene.
Application
Anti-Frizzled-1 antibody is suitable for immunohistochemistry studies (formalin-fixed, paraffin-embedded sections) at a concentration of 4μg/mL, using human kidney.
Biochem/physiol Actions
Frizzled homolog protein (FZD) is a seven-pass transmembrane type receptor expressed in various normal tissues such as skeletal muscle, kidney, pancreas, cerebellum and cerebral cortex. In human, ten members (FZD1-FZD10) of Frizzled homolog protein have been identified. Frizzled 1 (FZD1) protein is an essential component of the Wnt/β-catenin pathway. It is expressed in heart, kidney, lung, ovary, pancreas, placenta, and prostate. It has been reported that, FZD1 is up-regulated in several cancers including colon, ovarian, breast neuroblastoma.
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Multidrug resistance (MDR) represents a major obstacle in the successful treatment of breast cancer. The MDR1 gene is a direct target of the Wnt/β-catenin signaling pathway, which controls tumor development. Overexpression of P-glycoprotein, encoded by the MDR1 gene, is one
International journal of cancer, 132(8), 1731-1740 (2012-07-27)
Wnt signaling pathways play important roles in tumorigenesis and are initiated by binding of Wnt to various receptors including frizzleds (FZDs). FZDs are one of several families of receptors comprised of FZD/LRP/ROR2/RYK in the Wnt signaling pathway. Expression of some
International journal of oncology, 19(4), 767-771 (2001-09-20)
Frizzled (FZD) genes encode seven-transmembrane type WNT receptors, which are implicated in carcinogenesis and embryogenesis. We have previously cloned and characterized FZD1, FZD2, FZD3, FZD4, FZD5, FZD6, FZD7, FZD8, and FZD10. Here, we investigated expression profiles of all members of
Frizzled homolog 3 receptor was up-regulated in several gastrointestinal cancers such as esophageal and gastric cancers. Moreover, frizzled homolog 3 has recently reported to be expressed in colorectal adenoma specimens. In the present study, we investigated the clinical significance of
Cancer stem cell media, spheroid plates and cancer stem cell markers to culture and characterize CSC populations.
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