Team:Paris/August 16
From 2008.igem.org
(Difference between revisions)
(→Cleaning of the DNA after the digestion) |
(→List of ligations) |
||
Line 58: | Line 58: | ||
==='''List of ligations'''=== | ==='''List of ligations'''=== | ||
+ | |||
+ | * We ligated the DNA following the [[Team:Paris/Notebook/Protocols#Ligation|standard protocol]]. | ||
+ | * T1, T2, T3 and T4 are the autoligation controls for L 143, L144, L145 and L147 | ||
+ | |||
+ | {| style="text-align: center;" Border="2" | ||
+ | |'''Ligation name''' | ||
+ | |'''Insert name ''' | ||
+ | |'''Volume of insert µL''' | ||
+ | |'''Vector name''' | ||
+ | |'''Volume of Vector 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 | ||
+ | |} | ||
+ | |||
==='''Protocol'''=== | ==='''Protocol'''=== | ||
Revision as of 14:51, 17 August 2008
Analysis of the transformation we did yesterdayL143, L144, T1 and T2 showed no colonies. The positive control with pUC19 worked well.
LigationCleaning of the DNA after the digestionWe used the QIAcube to wash the DNA, following the standard protocol. Measure of DNA concentration of the digestion productsWe used the biophotometer.
List of ligations
ProtocolTransformation
|