LMA2L Rabbit Polyclonal Antibody, 50ul Cell Biology An important paralog of this

An important paralog of this gene is COL8A1

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

We offer comprehensive virus packaging services

This gene encodes apolipoprotein A-I

Megakaryocyte potentiating factor functions as a cytokine that can stimulate colony formation of bone marrow megakaryocytes

LMA2L Rabbit Polyclonal Antibody, 50ul Cell Biology An important paralog of thisThis 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