FBN3 Rabbit Polyclonal Antibody, 50ul Recombinant Ab Production Mutations in CUBN may play

Mutations in CUBN may play a role in autosomal recessive megaloblastic anemia

controlling heart rate and releasing oxytocin and vasopressin

Mutations in this gene are associated with anterior segment mesenchymal dysgenesis and congenital primary aphakia

This gene encodes the largest non-ATPase subunit of the 19S regulator lid| which is responsible for substrate recognition and binding

Cytochrome b5 type A encoded by CYB5A is a membrane-bound cytochrome that reduces ferric hemoglobin (methemoglobin) to ferrous hemoglobin

FBN3 Rabbit Polyclonal Antibody, 50ul Recombinant Ab Production Mutations in CUBN may playThis gene encodes a memebr of the fibrillin protein family. Fibrillins are extracellular matrix molecules that assemble into microfibrils in many connective tissues. This gene is most highly expressed in fetal tissues and its protein product is localized to extracellular microfibrils of developing skeletal elements skin lung kidney and skeletal muscle. This gene is potentially involved in Weill Marchesani syndrome.