IL-17 Rabbit Polyclonal Antibody, 100ul[BT-AP10566] Peptide Modification Kniest dysplasia

Kniest dysplasia

Containing six NHR (neuralized homology repeat) domains

Mutations in this gene result in malonyl-CoA decarboyxlase deficiency

cyclin L1 can be overexpressed and is therefore often considered a proto-oncogene

and may play an important role in liver carcinogenesis

IL-17 Rabbit Polyclonal Antibody, 100ul[BT-AP10566] Peptide Modification Kniest dysplasiaInduces stromal cells to produce proinflammatory and hematopoietic cytokines. Enhances the surface expression of the intracellular adhesion molecule 1 (ICAM 1) in fibroblasts. online information: Interleukin 17 entry PTM: Found both in glycosylated and nonglycosylated forms. Belongs to the IL 17 family. subunit: Homodimer. tissue specificity: Restricted to activated memory T cells.