IL-17 Rabbit Polyclonal Antibody, 100ul[BT-AP10566] Peptide Modification Autosomal recessive hypothalamic corticotropin deficiency

Autosomal recessive hypothalamic corticotropin deficiency has multiple and potentially fatal metabolic consequences including hypoglycemia and hepatitis

Mutations in this gene result in malonyl-CoA decarboyxlase deficiency

Displays antiviral activity against influenza A virus by inhibiting the budding of the virus from the plasma membrane by disturbing the lipid rafts

which does not change the protein sequence

IL-17 Rabbit Polyclonal Antibody, 100ul[BT-AP10566] Peptide Modification Autosomal recessive hypothalamic corticotropin deficiencyInduces 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.