CD56 Polyclonal Antibody, 50ul[BT-AP01516] Contamination Detection & Removal Mutations in ACTA1 cause nemaline

Mutations in ACTA1 cause nemaline myopathy type 3

The encoded protein is an integral membrane protein and may be localized to the basolateral membrane

Certain mutations in this gene have been associated with idiopathic generalized epilepsy (IGE)

This gene encodes a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene

This gene encodes a large protein that resides in the limiting membrane of endosomes and lysosomes and mediates intracellular cholesterol trafficking via binding of cholesterol to its N-terminal domain

CD56 Polyclonal Antibody, 50ul[BT-AP01516] Contamination Detection & Removal Mutations in ACTA1 cause nemalineNCAM1 (neural cell adhesion molecule 1) encodes a cell adhesion protein which is a member of the immunoglobulin superfamily. The encoded protein is involved in cell to cell interactions as well as cell matrix interactions during development and differentiation. The encoded protein has been shown to be involved in development of the nervous system, and for cells involved in the expansion of T cells and dendritic cells which play an important role in