LMA2L Rabbit Polyclonal Antibody, 50ul Cell Biology It functions as an anchoring

It functions as an anchoring fibril between the external epithelia and the underlying stroma

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

An important paralog of this gene is COL8A1

and susceptibility to virus and parasite

functional heterodimer which enhances protein folding in an ATP-dependent manner

LMA2L Rabbit Polyclonal Antibody, 50ul Cell Biology It functions as an anchoringThis 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