Difference between revisions of "Team:Rice/InterLab"
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<h1>InterLab</h1> | <h1>InterLab</h1> | ||
| + | <h2> Introduction </h2> | ||
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| + | <p> | ||
| + | This year, teams participating in the Interlab Study had to transform eight DNA test devices (see Table 1 below) provided in the distribution kit into E. coli DH5α cells and measure GFP fluorescence of the cells at four different time points. The purpose of the Interlab Study was to assess the reproducibility of fluorescence measurements across different labs and identify possible sources of variation in results obtained when following a common protocol. To determine possible sources of variation, the six test devices include all of the combinations of 3 related constitutive promoters with either the RBS B0034 or the bicistronic design element J364100. | ||
| + | </p> | ||
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</body> | </body> | ||
Revision as of 19:46, 18 October 2017
InterLab
Introduction
This year, teams participating in the Interlab Study had to transform eight DNA test devices (see Table 1 below) provided in the distribution kit into E. coli DH5α cells and measure GFP fluorescence of the cells at four different time points. The purpose of the Interlab Study was to assess the reproducibility of fluorescence measurements across different labs and identify possible sources of variation in results obtained when following a common protocol. To determine possible sources of variation, the six test devices include all of the combinations of 3 related constitutive promoters with either the RBS B0034 or the bicistronic design element J364100.
