EC Number   |
Application |
Reference  |
|---|
   1.14.14.3 | analysis |
enzyme can be used to monitor changes in gene expression as a reporter system in slow-growing mycobacteria, i.e. Mycobacterium tuberculosis strain H37Ra, determination of recombinant enzyme decay rate |
658778 |
| 1.14.14.3 | molecular biology |
enzyme can be used to monitor changes in gene expression as a reporter system in slow-growing mycobacteria, i.e. Mycobacterium tuberculosis strain H37Ra, determination of recombinant enzyme decay rate |
658778 |
| 1.14.14.3 | biotechnology |
establishment and evaluation of the enzyme used in a luciferase-based reporter system, pPL2lux, harboring the listerial secA and hlyA promoters translationally fused to luxABCDE, overview |
671457 |
| 1.14.14.3 | analysis |
expression of the bacterial luciferase system in mammalian cells for generation of bioreporters for in vivo monitoring and diagnostics technology, method evaluation and optimization, overview |
675217 |
| 1.14.14.3 | diagnostics |
expression of the bacterial luciferase system in mammalian cells for generation of bioreporters for in vivo monitoring and diagnostics technology, method evaluation and optimization, overview |
675217 |
| 1.14.14.3 | analysis |
high-throughput, homogeneous, bioluminescent assay for Pseudomonas aeruginosa gyrase inhibitors and other DNA-damaging agents based on a Photorhabdus luminescens luciferase operon transcriptional fusion to a promoter that responds to DNA damage caused by reduced gyrase levels and fluoroquinoline inhibition |
680943 |
| 1.14.14.3 | analysis |
the enzyme is used as a reporter system tool for analysis of promoter and gene expression activity, overview |
-, 711341 |
| 1.14.14.3 | molecular biology |
the enzyme is used as a reporter system tool for analysis of promoter and gene expression activity, overview |
-, 711341 |
| 1.14.14.3 | biotechnology |
the enzyme and cyanine fluorescent protein are useful dual reporters for the quantitative analysis of the effects of n-dodecyltrimethylammonium bromide on whole cells and intracellular proteins of Pseudomonas putida |
726764 |
| 1.14.14.3 | agriculture |
engineering of broad-host-range Erwinia amylovora virus Y2 to enhance its killing activity and for use as a luciferase reporter phage. The reporter phage Y2::luxAB transduces bacterial luciferase into host cells and induces synthesis of large amounts of a LuxAB luciferase fusion. After the addition of aldehyde substrate, bioluminescence can be monitored, and enables rapid and specific detection of low numbers of viable bacteria |
744110 |
