AKAP 13 Polyclonal Antibody, 20ul Immune Cell Preparation Mutations in ACTA1 cause nemaline

Mutations in ACTA1 cause nemaline myopathy type 3

with dysregulation linked to cancer

Each 50ml pipet is individually vacuum-packed for maximum sterility and color-coded for easy identification

Diseases associated with ACER3 include partial fetal alcohol syndrome and posterior amorphous corneal dystrophy

AKAP 13 Polyclonal Antibody, 20ul Immune Cell Preparation Mutations in ACTA1 cause nemalineThe A kinase anchor proteins (AKAPs) are a group of structurally diverse proteins which have the common function of binding to the regulatory subunit of protein kinase A (PKA) and confining the holoenzyme to discrete locations within the cell. This gene encodes a member of the AKAP family. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms containing c terminal dbl oncogene homology (DH) and