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EC Number Cloned (Commentary) Reference
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.3ligated into pET21-b vector, expressed from pZCH2 in Escherichia coli BL21 (lambdaDE3) cell line 704579
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.3luxCDABE operon, genetic organization, overview 711341
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.3overexpression in Escherichia coli 348606
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.3overexpression of mutant in XL1 blue MRF' cell line 348608
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.3overexpression of wild-type and mutant enzymes in Escherichia coli strain JM101 671978
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.3stable expression, using a bicistronic expression vector, of wild type luxA and luxB, WTA/WTB, codon-optimized luxA and wild type luxB, COA/WTB, and codon-optimized versions of both luxA and luxB genes, COA/COB, in HEK-293 cells, expression analysis, method evaluation and optimization, highest bioluminescence by expression of both codon-optimized genes, overview 675217
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.3the bacterial luciferase lux gene cassette consists of five genes, luxCDABE. The lux operon is re-synthesized through a process of multibicistronic, codon-optimization to demonstrate self-directed bioluminescence emission in a mammalian HEK-293 cell line in vitro and in vivo, overview. To overcome the limitations by FMNH2 supply, co-expression of a constitutively expressed flavin reductase gene frp from Vibrio harveyi is performed leading to a 151fold increased increase in bioluminescence in cells expressing mammalian codon-optimized luxCDE and frp genes 713371
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