From 2008.igem.org
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| | |pUC19 | | |pUC19 |
| | |Amp | | |Amp |
| | + | |} |
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| | + | ===Digetion checkin from yesterday=== |
| | + | |
| | + | [[Team:Paris/Notebook/Protocols#Digestion|Protocol Digestion]] |
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| | + | {| border="1" style="text-align: center" |
| | + | |Digestion name |
| | + | |Plasmid |
| | + | |Description |
| | + | |Miniprep used |
| | + | |Comments |
| | + | |- |
| | + | | |
| | + | |MP3 |
| | + | |B0015 (double terminator B0010-B0012) |
| | + | |4 |
| | + | |EcoRI and XbaI |
| | + | |- |
| | + | |D164 |
| | + | |MP101 |
| | + | |promoter J23101 |
| | + | |1 |
| | + | |SpeI and PstI |
| | + | |- |
| | + | |D161 |
| | + | |MP104 |
| | + | |PTet (Tet promoter) |
| | + | |1 |
| | + | |SpeI and PstI |
| | + | |- |
| | + | |D162 |
| | + | |MP114 |
| | + | |TetR |
| | + | |1 |
| | + | |EcoRI and SpeI |
| | + | |- |
| | + | |D163 |
| | + | |MP143 |
| | + | |gfp generator |
| | + | |2 |
| | + | |SpeI and PstI |
| | |} | | |} |
Revision as of 10:42, 19 August 2008
|
← Yesterday ↓ Calendar ↑Tomorrow →
Analysis of the transformation we did yesterday
L143, L144, T1 and T2 showed no colonies. The positive control with pUC19 worked well.
We suppose that the ligation did not work. We will do it again today.
for Kok-Phen Ligations
Cleaning of the DNA after the digestion
We used the QIAcube to wash the DNA, following the standard protocol.
Measure of DNA concentration of the digestion products
We used the biophotometer.
Settings:
- 10 µL of template DNA in 50 µL of pure water
- Blank : 10 µL of EB buffer in 50 µL of water.
| Digestion name
| What's in ?
| DNA concentration (ng/µL)
|
| D 158
| OmpR*
| 12
|
| D 159
| EnvZ*
| 7
|
| D 102
| B0034
| 16
|
List of ligations
- We ligated the DNA following the standard protocol.
- T5 is the autoligation control for L148 and L149.
| Ligation name
| Insert name
| Vinsert µL
| Vector name
| VVector µL
|
| L 148 (Amp)
| D 158 (OmpR*)
| 4
| D 102 (B0034)
| 3
|
| L 149 (Amp)
| D 159 (EnvZ)
| 7
| D 102 (B0034)
| 3
|
Ligation
Cleaning of the DNA after the digestion
We used the QIAcube to wash the DNA, following the standard protocol.
Measure of DNA concentration of the digestion products
We used the biophotometer.
Settings:
- 10 µL of template DNA in 50 µL of pure water
- Blank : 10 µL of EB buffer in 50 µL of water.
| Digestion name
| What's in ?
| DNA concentration (ng/µL)
|
| D 149
| pfliL
| 2
|
| D 150
| pfliL
| 3
|
| D 151
| pSB3K3
| 12
|
| D 152
| pSB3K3
| 20
|
| D 153
| gene flhDC
| 7
|
| D 154
| gene flhDC
| 12
|
| D 155
| pflhDC
| 16
|
| D 136
| j61002
| 12
|
| D 145
| pSB1A2
| 21
|
List of ligations
- We ligated the DNA following the standard protocol.
- T1, T2, T3 and T4 are the autoligation controls for L 143, L144, L145 and L147
| Ligation name
| Insert name
| Vinsert µL
| Vector name
| VVector µL
|
| L 143 (Kan)
| D 149 (pfliL)
| 8
| D 137 (pSB3K3)
| 4
|
| L 144 (Kan)
| D 150 (pfliL)
| 5
| D 152 (pSB3K3)
| 2.5
|
| L 145 (Amp)
| D 153 (g flhDC)
| 10
| D 145 (pSB1A2)
| 2.5
|
| L 146 (Amp)
| D 154 (g flhDC)
| 5
| D 145 (pSB1A2)
| 2.5
|
| L 147 (Amp)
| D 155 (p flhDC)
| 1
| D 136 (J61002)
| 4
|
Transformation
Transformation protocol
| Name
| Description
| Antibio
|
| Ligations
|
| L150
| D105(BV) - D146(BI)
pLas - strongest rbs-TetR-GFP tripart
| Amp
|
| L151
| D147(FI) - D125 (FV)
strongest rbs-LasR activator with LVA - Double terminator
| Kan
|
| Controls
|
| C1
| D105
| Amp
|
| C2
| D125
| Kan
|
| Positive Control
| pUC19
| Amp
|
Digetion checkin from yesterday
Protocol Digestion
| Digestion name
| Plasmid
| Description
| Miniprep used
| Comments
|
|
| MP3
| B0015 (double terminator B0010-B0012)
| 4
| EcoRI and XbaI
|
| D164
| MP101
| promoter J23101
| 1
| SpeI and PstI
|
| D161
| MP104
| PTet (Tet promoter)
| 1
| SpeI and PstI
|
| D162
| MP114
| TetR
| 1
| EcoRI and SpeI
|
| D163
| MP143
| gfp generator
| 2
| SpeI and PstI
|
|
"
