From 2008.igem.org
(Difference between revisions)
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| Line 200: |
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| | |MP3 | | |MP3 |
| - | |B0015 (double terminator B0010-B0012) | + | |B0015 (double terminator B0010-B0012) - FV |
| | |4 | | |4 |
| - | |EcoRI and XbaI | + | |No bands |
| | |- | | |- |
| | |D164 | | |D164 |
| | |MP101 | | |MP101 |
| - | |promoter J23101 | + | |promoter J23101 - BV |
| | |1 | | |1 |
| - | |SpeI and PstI | + | |Good expected sized bands |
| | |- | | |- |
| | |D161 | | |D161 |
| | |MP104 | | |MP104 |
| - | |PTet (Tet promoter) | + | |PTet (Tet promoter) - FI |
| | |1 | | |1 |
| - | |SpeI and PstI | + | |Good expected sized band |
| | |- | | |- |
| | |D162 | | |D162 |
| | |MP114 | | |MP114 |
| - | |TetR | + | |TetR - BI |
| | |1 | | |1 |
| - | |EcoRI and SpeI | + | |Good expected sized bands |
| | |- | | |- |
| | |D163 | | |D163 |
| | |MP143 | | |MP143 |
| - | |gfp generator | + | |gfp generator - BV |
| | |2 | | |2 |
| - | |SpeI and PstI | + | |Good expected sized bands |
| | |} | | |} |
Revision as of 10:47, 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 check from yesterday
Protocol Digestion
| Digestion name
| Plasmid
| Description
| Miniprep used
| Comments
|
|
| MP3
| B0015 (double terminator B0010-B0012) - FV
| 4
| No bands
|
| D164
| MP101
| promoter J23101 - BV
| 1
| Good expected sized bands
|
| D161
| MP104
| PTet (Tet promoter) - FI
| 1
| Good expected sized band
|
| D162
| MP114
| TetR - BI
| 1
| Good expected sized bands
|
| D163
| MP143
| gfp generator - BV
| 2
| Good expected sized bands
|
|
"
