P38 mouse Monoclonal Antibody(8C11), 20ul Filtration Mutations in this gene are

Mutations in this gene are associated with type II autosomal recessive Alport syndrome (hereditary glomerulonephropathy) and with familial benign hematuria (thin basement membrane disease)

including STAT1 and STAT2

Because many of the tissues and structures affected in VCFS/DGS derive from the pharyngeal arches of the developing embryo

gamma 1 chain is necessary for laminin heterotrimer assembly

P38 mouse Monoclonal Antibody(8C11), 20ul Filtration Mutations in this gene areThe protein encoded by this gene is a member of the MAP kinase family. MAP kinases act as an integration point for multiple biochemical signals, and are involved in a wide variety of cellular processes such as proliferation, differentiation, transcription regulation and development. This kinase is activated by various environmental stresses and proinflammatory cytokines. The activation requires its phosphorylation by MAP kinase kinases (MKKs), or its