P38 mouse Monoclonal Antibody(8C11), 20ul Filtration Get ready to push boundaries

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

Mutations in DRD4 have been associated with various behavioral phenotypes

P38 mouse Monoclonal Antibody(8C11), 20ul Filtration Get ready to push boundariesThe 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