MIA3 Polyclonal Antibody, 20ul Low-speed Centrifuges osteogenesis imperfecta and Charcot-Marie-Tooth Disease

osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3

DNA methylation differences have been found in this gene in monozygotic twins that are discordant for adolescent depression

resulting from alternative splicing of the precursor mRNA

Both p105 and p100 are proteolytically processed by the proteasome to produce p50 and p52

This protein mediates the expression of a variety of genes in response to cell stimuli

MIA3 Polyclonal Antibody, 20ul Low-speed Centrifuges osteogenesis imperfecta and Charcot-Marie-Tooth DiseaseAlthough 2 transmembrane domains are predicted, PubMed: 19269366 showed that it only contains one transmembrane domain. The other predicted transmembrane region is probably a hairpin type region embedded into the membrane, which does not cross the membrane. It is unclear which of the 2 predicted transmembrane regions is the transmembrane or the hairpin type region.,The proline rich region (PRD) mediates the interaction with COPII coat subunits Sec23