PAI-1 Polyclonal Antibody, 100ul Shakers characterized by oral

characterized by oral

this kit offers maximum stability with storage at 2-8℃

Mutations in this gene cause a multiple congenital anomaly syndrome in human patients

The encoded gene product presumably interacts with YY1 protein

Mutations in this gene are associated with autosomal recessive Bartter syndrome type 3 (BS3)

PAI-1 Polyclonal Antibody, 100ul Shakers characterized by oralSERPINE1 encodes a member of the serine proteinase inhibitor (serpin) superfamily. This member is the principal inhibitor of tissue plasminogen activator (tPA) and urokinase (uPA), and hence is an inhibitor of fibrinolysis. Defects in SERPINE1 are the cause of plasminogen activator inhibitor 1 deficiency (PAI 1 deficiency), and high concentrations of the gene product are associated with thrombophilia. Alternatively spliced transcript variants encoding