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Team:NYMU-Taipei/results/immunological-solution1
From 2011.igem.org
Contents |
Construction & Parts
Our minC Construct and Inv & LLO Construct on AMB-1
[http://partsregistry.org/wiki/index.php?title=Part:BBa_K624053 BBa_K624053]
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Related Parts We have created several PARTs on the basis of Biobrick. The expression will be shown on the partregistry webpage.
| [http://partsregistry.org/wiki/index.php?title=Part:BBa_K624033 BBa_K624033] | minC cell division inhibitor (revised) |
| [http://partsregistry.org/wiki/index.php?title=Part:BBa_K624034 BBa_K624034] | revised minC primer (forward) |
| [http://partsregistry.org/wiki/index.php?title=Part:BBa_K624035 BBa_K624035] | revised minC primer (reverse) |
| [http://partsregistry.org/wiki/index.php?title=Part:BBa_K624036 BBa_K624036] | minC+mcherry |
| [http://partsregistry.org/wiki/index.php?title=Part:BBa_K624037 BBa_K624037] | rbs+minC+mcherry |
| [http://partsregistry.org/wiki/index.php?title=Part:BBa_K624040 BBa_K624040] | pT7-tetO+RBS+minC |
| [http://partsregistry.org/wiki/index.php?title=Part:BBa_K624045 BBa_K624045] | Pmsp1(tetO) + RBS(Pmsp3) + minC + RBS(Pmsp3) + mcherry |
| [http://partsregistry.org/wiki/index.php?title=Part:BBa_K624056 BBa_K624056] | pYMB essentials + RBS(Pmsp3) + minC |
| [http://partsregistry.org/wiki/index.php?title=Part:BBa_K624057 BBa_K624057] | pYMB essentials + RBS(Pmsp3) + LLO |
| [http://partsregistry.org/wiki/index.php?title=Part:BBa_K624058 BBa_K624058] | pYMB essentials + RBS(Pmsp3) + Inv |
Nested-PCR Primers For Various Strains
nested-Inv
| [http://partsregistry.org/wiki/index.php?title=Part:BBa_K624063 BBa_K624063] | nested_Inv F (inter-strain nested primer) |
| [http://partsregistry.org/wiki/index.php?title=Part:BBa_K624064 BBa_K624064] | nested_Inv R (inter-strain nested primer) |
nested-LLO
| [http://partsregistry.org/wiki/index.php?title=Part:BBa_K624065 BBa_K624065] | nested_LLO F (inter-strain nested primer) |
| [http://partsregistry.org/wiki/index.php?title=Part:BBa_K624066 BBa_K624066] | nested_LLO R (inter-strain nested primer) |
Symbiosis with Human Glial Cell
Magnetotactic bacteria were introduced into guanulocytes and monocytes by phagocytosis.(Tadashi Matsunaga et all. 1986)
In order to simulate the circumstances in brain, we put AMB-1 separately into mixed glial cells in vitro. Below are the photos we captured under microscope.
check out [http://partsregistry.org/wiki/index.php?title=Part:BBa_K624032 BBa_K624032] for detailed characterization
| File:AMB-1 glial1.tif | File:AMB-1 glial2.tif |
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| File:Glial1.tif | File:Glial2.tif |
Measurements of Construct tetR+rbs+gfp under Fluorescence Microscope
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These are the measurements of our construct [http://partsregistry.org/wiki/index.php?title=Part:BBa_K624001 tetR+rbs+GFP](BBa_K624001) under fluorescence microscope. The left graph is from the control group of E. coli strain DH5-alpha. The middle is tetR+rbs+gfp in plasmid pSB1C3 in E. coli, while the right is from a plate without any bacilli. All graphs are measured in fixed exposure time. Construct of tetR+rbs+gfp which emits light is thought to be a leak phenomenon of plasmid, while RE digest has proved that the sequence length is correct, and further sequencing work is under operation.
gfp measurements under different excitation wavelengths
The expression of gfp is measured precisely under excitation wavelength from 475nm to 501nm, given the absorption wavelength 511nm. In our measurement, wavelength over 493nm yields high background, resulting in values of control group surging far beyond normal condition. Thus, 493nm is suggested as the best excitation wavelength, as it presents the highest emission light and the lowest of the control group.
