Difference between revisions of "Part:BBa K2797006"
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===Newcastle 2018 - Interlab Characterisation=== | ===Newcastle 2018 - Interlab Characterisation=== | ||
− | Three further InterLab studies were carried out using mNeonGreen expressing E. coli DH5-alpha. These contained the original test devices from the iGEM 2018 distribution kit (Anderson Promoter Collection), using the same conditions as the original study. The fluorescein/OD of the mNeonGreen study was compared to the original InterLab test device data by using a fluorescein standard curve. | + | Three further InterLab studies were carried out using mNeonGreen expressing <i>E. coli</i> DH5-alpha. These contained the original test devices from the iGEM 2018 distribution kit (Anderson Promoter Collection), using the same conditions as the original study. The fluorescein/OD of the mNeonGreen study was compared to the original InterLab test device data by using a fluorescein standard curve. |
Figure 1 shows the fluorescein/OD values of the original InterLab devices (GFPmut3b) vs the mNeonGreen test devices. Test device 3, in both the original and mNeonGreen experiment, has the weakest promoter (J23117) and thus shows the lowest fluorescein/OD. However, it can still be observed that the mNeonGreen reporter shows bother a higher fluorescein/OD and a lower spread of data - indicating that mNeonGreen may be a useful alternate reporter to GFPmut3b for the InterLab study and part characterisation. | Figure 1 shows the fluorescein/OD values of the original InterLab devices (GFPmut3b) vs the mNeonGreen test devices. Test device 3, in both the original and mNeonGreen experiment, has the weakest promoter (J23117) and thus shows the lowest fluorescein/OD. However, it can still be observed that the mNeonGreen reporter shows bother a higher fluorescein/OD and a lower spread of data - indicating that mNeonGreen may be a useful alternate reporter to GFPmut3b for the InterLab study and part characterisation. |
Latest revision as of 15:03, 17 October 2018
Test Device 3 for the iGEM InterLab Study (mNeonGreen)
BBa_K2797006, test device 3 (originally BBa_J364002) for the iGEM 2018 InterLab study with mNeonGreen replacing the GFP fluorescent reporter. Each mNeonGreen test device retains the same promoter, RBS and terminator of each of their corresponding InterLab test device vectors, with the only change being mNeonGreen replacing the GFPmut3b.
Usage and Biology
The mNeonGreen protein is widely used in the imaging of cellular components due to it having a fluorescence 3-5 times that of GFP. Importantly however, it is thought to be more photostable than the mut3GFP used in the InterLab study, although there is little indication in the literature that it has been used as a reporter for the characterisation of circuits. Replacing mut3GFP with mNeonGreen allowed the investigation of whether the fast folding capabilities coupled with its brightness and higher photostability could yield a lower spread of fluorescence values in regard to the original mut3GFP, making it a better tool for part characterisation.
Newcastle 2018 - Interlab Characterisation
Three further InterLab studies were carried out using mNeonGreen expressing E. coli DH5-alpha. These contained the original test devices from the iGEM 2018 distribution kit (Anderson Promoter Collection), using the same conditions as the original study. The fluorescein/OD of the mNeonGreen study was compared to the original InterLab test device data by using a fluorescein standard curve.
Figure 1 shows the fluorescein/OD values of the original InterLab devices (GFPmut3b) vs the mNeonGreen test devices. Test device 3, in both the original and mNeonGreen experiment, has the weakest promoter (J23117) and thus shows the lowest fluorescein/OD. However, it can still be observed that the mNeonGreen reporter shows bother a higher fluorescein/OD and a lower spread of data - indicating that mNeonGreen may be a useful alternate reporter to GFPmut3b for the InterLab study and part characterisation.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 39
- 1000COMPATIBLE WITH RFC[1000]