Na+/K+-ATPase Alpha1 Polyclonal Antibody, 50ul[BT-AP05760] Oligo Pool Mutations in this gene cause

Mutations in this gene cause Leigh syndrome due to mitochondrial complex I deficiency

The protein encoded by this gene is a cytoplasmic nonreceptor protein kinase which may function as an intracellular signal transducer in epithelial tissues

The product of this gene forms homomeric complexes and heteromeric complexes with other activated Smad proteins

Studies in mouse suggest that nuclear matrix transcription factors (NP/NMP4) may be part of a general mechanical pathway that couples cell construction and function during extracellular matrix remodeling

Src family tyrosine kinase) contains N-terminal sites for myristylation and palmitylation

Na+/K+-ATPase Alpha1 Polyclonal Antibody, 50ul[BT-AP05760] Oligo Pool Mutations in this gene causeSodium potassium transporting ATPase subunit alpha 1 encoded by ATP1A1 belongs to the family of P type cation transport ATPases, and to the subfamily of Na+ K+ ATPases. Na+ K+ ATPase is an integral membrane protein responsible for establishing and maintaining the electrochemical gradients of Na and K ions across the plasma membrane. These gradients are essential for osmoregulation, for sodium coupled transport of a variety of organic and inorganic