S20A2 Rabbit Polyclonal Antibody, 20ul Cell fragmentation and collection Defects in this factor lead

Defects in this factor lead to Rosenthal syndrome| a blood coagulation abnormality

and studies in mice show that overexpression of GSK3B may be relevant to the pathogenesis of Alzheimer disease

This protein is required for TNF-alpha-mediated activation of MAPK8/JNK and NF-kappaB

and gamma families

S20A2 Rabbit Polyclonal Antibody, 20ul Cell fragmentation and collection Defects in this factor leadThis gene encodes a member of the inorganic phosphate transporter family. The encoded protein is a type 3 sodium dependent phosphate symporter that plays an important role in phosphate homeostasis by mediating cellular phosphate uptake. The encoded protein also confers susceptibility to viral infection as a gamma retroviral receptor. Mutations in this gene may play a role in familial idiopathic basal ganglia calcification. Alternatively spliced