Sec16A Polyclonal Antibody, 100ul Sampling Tubes In one family with congenital

In one family with congenital myasthenic syndrome affecting limb-girdle muscles| a mutation in this gene was found

0 mL Sterile Lid Lock Micro centrifuge Tubes

Upon erythropoietin binding

Mutations in this gene are associated with hypochromic microcytic anemia with iron overload

Sec16A Polyclonal Antibody, 100ul Sampling Tubes In one family with congenitalThis gene encodes a protein that forms part of the Sec16 complex. This protein has a role in protein transport from the endoplasmic reticulum (ER) to the Golgi and mediates COPII vesicle formation at the transitional ER. Alternative splicing results in multiple transcript variants that encode different protein isoforms.