Team:Paris/August 15

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==Analysis of yesterday PCR screening==
==Analysis of yesterday PCR screening==

Revision as of 09:35, 16 August 2008

← Yesterday

↓ Calendar ↑

Tomorrow →

Contents

Transformation of the ligations we did yesterday

We transformed L 143, L 144 and the negative controls T1 and T2, using Invitrogen's TOP10 chemically competent cells
standard protocol.


Digestion

Measurement of concentration of minipreps

standard protocol

Digestion Miniprep used Concentration (µg/mL) ratio 260/280
D146 MP148.2 123 1.58
D147 MP153.3 113 1.68


Digestion

Protocol Digestion


Ligation

Protocol Ligation

Ligation name Insert Vector
L143 D146 (strongest rbs-TetR-GFP tripart) D105 (pLas)
L144 D147 (strongest rbs-LasR activator with LVA) D125 (Double terminator)


Analysis of yesterday PCR screening

KR000163.jpg KR000162.jpg KR000164.jpg


Starting the construction of the Promoter characterization plasmid

Digestion

Measurement of concentration of minipreps

standard protocol

Plasmid Miniprep Concentration (µg/mL) ratio 260/280
MP3 3 152 1.43
MP3 4 775 1.21
MP101 1 317 1.66
MP101 2 389 1.36
MP101 4 209 1.76
MP104 1 173 1.32
MP104 3 43 1.85
MP104 4 52 1.66
MP114 1 173 1.75
MP114 2 263 1.43
MP143 1 133 1.55
MP143 2 132 1.70

Digestion

Protocol Digestion

Plasmid Description Miniprep used Enzymes
MP3 B0015 (double terminator B0010-B0012) 4 EcoRI and XbaI
MP114 TetR 1 EcoRI and SpeI
MP104 PTet (Tet promoter) 1 SpeI and PstI
MP101 promoter J23101 1 SpeI and PstI
MP143 gfp generator 2 SpeI and PstI
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