MOG Polyclonal Antibody, 100ul Molecular Sciences and hearing loss

and hearing loss

This gene encodes a possible magnesium transporter

One type of mutation responsible for EPM1 is the expansion in the promoter region of this gene of a CCCCGCCCCGCG rep

The protein encoded by this gene belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family

MOG Polyclonal Antibody, 100ul Molecular Sciences and hearing lossThe product of this gene is a membrane protein expressed on the oligodendrocyte cell surface and the outermost surface of myelin sheaths. Due to this localization, it is a primary target antigen involved in immune mediated demyelination. This protein may be involved in completion and maintenance of the myelin sheath and in cell cell communication. Alternatively spliced transcript variants encoding different isoforms have been identified.