MOT1 Polyclonal Antibody, 100ul Vacuum Filter In cases of Prader-Willi syndrome

In cases of Prader-Willi syndrome

Barrett's esophagus as well as in gastric metaplasia of the duodenum (GMD)

This gene is intronless and encodes a replication-dependent histone that is a member of the histone H1 family

This gene encodes a protein involved in processing the signal peptide sequences used to direct mitochondrial proteins to the mitochondria

The cleavage of p35 into p25 results in relocalization of the protein from the cell periphery to nuclear and perinuclear regions

MOT1 Polyclonal Antibody, 100ul Vacuum Filter In cases of Prader-Willi syndromeThe protein encoded by this gene is a proton linked monocarboxylate transporter that catalyzes the movement of many monocarboxylates, such as lactate and pyruvate, across the plasma membrane. Mutations in this gene are associated with erythrocyte lactate transporter defect. Alternatively spliced transcript variants have been found for this gene.