CD236 Polyclonal Antibody, 100ul RNA Synthesis Defects in this gene are

Defects in this gene are a cause of epilepsy female-restricted with mental retardation (EFMR)

our tips are DNase/RNase-free and pyrogen-free

This gene encodes a 39S subunit protein that belongs to the L22 ribosomal protein family

Mutations in this gene are associated with hypoparathyroidism

This gene encodes a member of the CRMP (collapsing response mediator protein) family thought to be involved in neural development

CD236 Polyclonal Antibody, 100ul RNA Synthesis Defects in this gene areGlycophorin C (GYPC) is an integral membrane glycoprotein. It is a minor species carried by human erythrocytes, but plays an important role in regulating the mechanical stability of red cells. A number of glycophorin C mutations have been described. The Gerbich and Yus phenotypes are due to deletion of exon 3 and 2, respectively. The Webb and Duch antigens, also known as glycophorin D, result from single point mutations of the glycophorin C gene. The