MOT2 Polyclonal Antibody, 100ul Protein Modification Mutations in this gene have

Mutations in this gene have been associated with KBG syndrome| which is characterized by macrodontia| distinctive craniofacial features| short stature| skeletal anomalies| global developmental delay| seizures and intellectual disability

the first member of the antizyme family

The PCAF histone acetylase complex

and calcyclin

MOT2 Polyclonal Antibody, 100ul Protein Modification Mutations in this gene haveThis gene is a member of the monocarboxylate transporter family. Members in this family transport metabolites, such as lactate, pyruvate, and ketone bodies. The protein encoded by this gene catalyzes the proton linked transport of monocarboxylates and has the highest affinity for pyruvate. This protein has been reported to be more highly expressed in prostate and colorectal cancer specimens when compared to control specimens. Alternative splicing