Akt1 Polyclonal Antibody, 100ul[BT-AP00345] Shakers Mutations in TAZ have been

Mutations in TAZ have been associated with a number of clinical disorders including Barth syndrome

it should not be confused with the conventional non-muscle myosin-9 (MYH9)

This gene product is a key molecule in ion channel regulation and synaptic exocytosis

and it is involved in the control of cell shape

docosahexaenoic acid

Akt1 Polyclonal Antibody, 100ul[BT-AP00345] Shakers Mutations in TAZ have beenThe serine threonine protein kinase encoded by the AKT1 gene is catalytically inactive in serum starved primary and immortalized fibroblasts. AKT1 and the related AKT2 are activated by platelet derived growth factor. The activation is rapid and specific, and it is abrogated by mutations in the pleckstrin homology domain of AKT1. It was shown that the activation occurs through phosphatidylinositol 3 kinase. In the developing nervous system AKT is a