IL-17C Polyclonal Antibody, 100ul Cytokines Defects in this gene are

Defects in this gene are the cause of Werner syndrome| an autosomal recessive disorder characterized by premature aging

It has high structural and functional similarity to FK506-binding protein 1A (FKBP1A)

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WD repeat and HMG-box DNA-binding protein 1encoded by WDHD1 contains multiple N-terminal WD40 domains and a C-terminal high mobility group (HMG) box

IL-17C Polyclonal Antibody, 100ul Cytokines Defects in this gene areThe protein encoded by this gene is a T cell derived cytokine that shares the sequence similarity with IL17. This cytokine was reported to stimulate the release of tumor necrosis factor alpha and interleukin 1 beta from a monocytic cell line. The expression of this cytokine was found to be restricted to activated T cells.