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Found 2 matching solutions for this experiment
pMAPLe4
David Eisenberg, UCLA-DOE Institute for Genomics and Proteomics,
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The EsxEFma and EsxGHms cultures were grown for 18 hours at 18°C after induction of protein expression with 0.5 mM IPTG while the EsxOPmt culture was grown under the same conditions but protein expression was induced with 1.0 mM IPTG. |
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Protocol tips |
The EsxEFma and EsxGHms cultures were grown for 18 hours at 18°C after induction of protein expression with 0.5 mM IPTG while the EsxOPmt culture was grown under the same conditions but protein expression was induced with 1.0 mM IPTG. |
pMAPLe3
David Eisenberg, UCLA-DOE Institute for Genomics and Proteomics,
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Protocol tips |
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Briefly, E. coli BL21 (DE3) and/or E. coli Rosetta (DE3) harboring the expression plasmids were grown overnight in a 96 well block (Thomson Instrument Company, Oceanside, CA) at 37°C in 1 ml of LB media supplemented with 30 µg/ml kanamycin, and 34 µg/ml chloramphenicol for E. coli Rosetta (DE3), using a Shel Lab SI6R-HS shaking incubator with shaking at 650 rpm. The following day a 96 well block with 1 ml of fresh media supplemented with the appropriate antibiotics was inoculated with 50 µl of the overnight culture. The cultures were grown to an OD600 of 0.5 and protein expression induced by the addition of IPTG to a final concentration of 0.5 mM. |
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Protocol tips |
Briefly, E. coli BL21 (DE3) and/or E. coli Rosetta (DE3) harboring the expression plasmids were grown overnight in a 96 well block (Thomson Instrument Company, Oceanside, CA) at 37°C in 1 ml of LB media supplemented with 30 µg/ml kanamycin, and 34 µg/ml chloramphenicol for E. coli Rosetta (DE3), using a Shel Lab SI6R-HS shaking incubator with shaking at 650 rpm. The following day a 96 well block with 1 ml of fresh media supplemented with the appropriate antibiotics was inoculated with 50 µl of the overnight culture. The cultures were grown to an OD600 of 0.5 and protein expression induced by the addition of IPTG to a final concentration of 0.5 mM. |
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