PRPF31 Polyclonal Antibody, 20ul 3D Culture Mutations in NME1 have been
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PRPF31 Polyclonal Antibody, 20ul 3D Culture Mutations in NME1 have beenPRPF31 encodes a component of the spliceosome complex and is one of several retinitis pigmentosa causing genes. When the gene product is added to the spliceosome complex, activation occurs.
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