MYPC2 Polyclonal Antibody, 100ul sgRNA customized design a multisystem developmental disorder caused

a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11

Translocations involving this gene play a role in acute leukemia and extraskeletal myxoid chondrosarcoma

Mutation or amplification of this gene is associated with B-cell lymphomas

smooth muscle contraction

Expression of this particular cadherin in osteoblastic cell lines

MYPC2 Polyclonal Antibody, 100ul sgRNA customized design a multisystem developmental disorder causedThis gene encodes a member of the myosin binding protein C family. This family includes the fast , slow and cardiac type isoforms, each of which is a myosin associated protein found in the cross bridge bearing zone (C region) of A bands in striated muscle. The protein encoded by this locus is referred to as the fast type isoform. Mutations in the related but distinct genes encoding the slow type and cardiac type isoforms have been associated with