SEM6A Polyclonal Antibody, 100ul Polyclonal Antibodies 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

While the precise function of the encoded protein is currently unknown| it appears to be involved in mRNA turnover and ribosome assembly

translocation of part of the Y chromosome containing this gene to the X chromosome causes XX male syndrome

and by inhibiting protease activity in tissues undergoing remodelling of the extracellular matrix

These transmembrane receptors change conformation in response to their cognate neurotransmitter

SEM6A Polyclonal Antibody, 100ul Polyclonal Antibodies osteogenesis imperfecta and Charcot-Marie-Tooth DiseaseThe transmembrane semaphorin SEMA6A is expressed in developing neural tissue and is required for proper development of the thalamocortical projection (Leighton et al., 2001