LMA2L Rabbit Polyclonal Antibody, 50ul Cell Biology This gene encodes apolipoprotein A-I

This gene encodes apolipoprotein A-I

Alternate splicing of this gene results in two transcript variants encoding different proteins

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

the first intermediate in the biosynthetic pathway of GPI anchor

An important paralog of this gene is COL8A1

LMA2L Rabbit Polyclonal Antibody, 50ul Cell Biology This gene encodes apolipoprotein A-IThis gene encodes a protein belonging to the L type lectin group of type 1 membrane proteins which function in the mammalian early secretory pathway. These proteins contain luminal carbohydrate recognition domains which display homology to leguminous lectins. Unlike other proteins of the group which cycle in the early secretory pathway and are predominantly associated with post endoplasmic reticulum membranes the protein encoded by this gene is a non