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1 lding domain stabilizes the alpha subunit of bacterial luciferase.
2 inosa engineered to constitutively express a bacterial luciferase.
3 lucose-6-phosphate dehydrogenase (G6PDH) and bacterial luciferase.
4 l furnish a detailed molecular model for all bacterial luciferases.
6 rating the rate of the productive pathway of bacterial luciferase alphabeta heterodimer formation.
7 heteromeric protein complex composed of the bacterial luciferase and a 20-kDa lumazine binding prote
8 characterization of a catalytic residue for bacterial luciferase and the first demonstration of the
9 erent oxygen-dependent reporters, insect and bacterial luciferases, and two bacterial hosts, Gram (+)
13 fficient and is faster in generating CL than bacterial luciferase but requires the introduction of lu
14 ence assay couples NAD(+) consumption to the bacterial luciferase-catalyzed oxidation of decanal.
21 rate transcriptional fusions of promoterless bacterial luciferase genes, luxAB, to the Anabaena genom
22 ly of the heterodimeric flavin monooxygenase bacterial luciferase has been defined by a unique set of
28 chloroplast by synthesizing the two-subunit bacterial luciferase (lux)AB, as a single fusion protein
30 ns of 1-[1H]decanal and 1-[2H]decanal in the bacterial luciferase reaction was carried out, and aldeh
31 ow that within the Escherichia coli cytosol, bacterial luciferase subunits LuxA and LuxB assemble int
32 xyl steroid dehydrogenase coimmobilized with bacterial luciferase system and a chemiluminescence assa
33 e luxAB genes, encoding the reporter protein bacterial luciferase, to the hbp regulator-promoter sequ