AMPK Alpha1 Monoclonal Antibody(5G11), 100ul Immuno Plates 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)

This gene is one of the fifteen kallikrein subfamily members located in a cluster on chromosome 19

(S)-lactate from pyruvate: step 1/1

CEA family

Actins are highly conserved proteins that are involved in various types of cell motility and in the maintenance of the cytoskeleton

AMPK Alpha1 Monoclonal Antibody(5G11), 100ul Immuno Plates Mutations in this gene areThe protein encoded by this gene belongs to the ser thr protein kinase family. It is the catalytic subunit of the 5' prime AMP activated protein kinase (AMPK). AMPK is a cellular energy sensor conserved in all eukaryotic cells. The kinase activity of AMPK is activated by the stimuli that increase the cellular AMP ATP ratio. AMPK regulates the activities of a number of key metabolic enzymes through phosphorylation. It protects cells from stresses that