PON3 Polyclonal Antibody, 50ul Antibody Humanization rat and mouse

rat and mouse

Defects in this gene are the cause of Werner syndrome| an autosomal recessive disorder characterized by premature aging

The consensus recognition site is 5'-T

MED13 (mediator complex subunit 13) encodes a component of the mediator complex (also known as TRAP

PON3 Polyclonal Antibody, 50ul Antibody Humanization rat and mouseThis gene is a member of the paraoxonase family and lies in a cluster on chromosome 7 with the other two family members. The encoded protein is secreted into the bloodstream and associates with high density lipoprotein (HDL). The protein also rapidly hydrolyzes lactones and can inhibit the oxidation of low density lipoprotein (LDL), a function that is believed to slow the initiation and progression of atherosclerosis. Alternatively spliced variants