Difference between revisions of "Team:Paris Saclay/Notebook/August/14"
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Agarose gel 1%, Migration 90V | Agarose gel 1%, Migration 90V | ||
− | + | [[File:ParisSaclay 14.08.15-quantif(3).jpg|300px|center]] | |
+ | <html><p><i>Quantification, from left to right: 1. <a href="https://2015.igem.org/File:Paris_Saclay-Ladder.jpg" target="_blank">DNA Ladder</a>, 2. BBa_K1707011#3 (08/12), 3. BBa_K1707011#3 (08/12), 4. BBa_K1707012#2 (08/12), 5. BBa_K1707012#2 (08/13), 6. BBa_K1707033#1, 7. BBa_K1707033#2, 8. BBa_R0051 (2<sup>nd</nd> send), 9. Empty, 10. Empty</i></p></html> | ||
We can conclude: | We can conclude: | ||
* BBa_R0051 (2nd send): 13 µg/µL | * BBa_R0051 (2nd send): 13 µg/µL | ||
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Agarose gel, 1%, Migration 90V | Agarose gel, 1%, Migration 90V | ||
− | + | [[File:ParisSaclay 14.08.15-vérif.jpg|300px|center]] | |
+ | <html><p><i>Verification of gel purification, from left to right: 1. <a href="https://2015.igem.org/File:Paris_Saclay-Ladder.jpg" target="_blank">DNA Ladder</a>, 2. BBa_K1707030#3, 3. BBa_K1707031#4, 4. BBa_K1707031#5, 5. BBa_K1707031#6, 6. Empty, 7. Empty, 8. Empty, 9. Empty, 10. Empty</i></p></html> | ||
Biobricks: | Biobricks: | ||
* Verification: | * Verification: |
Latest revision as of 20:49, 18 September 2015
Contents
Friday 14th August
Lab Work
Quantification
by Pauline
- BBa_R0051 (2nd send)
- BBa_K1707011 #3
- BBa_K1707012 #2
- BBa_K1707033 #1 and #2
Mix:
- 2 µL plasmid
- 2 µL DNA Loading 6X
- 6 µL H2O
Agarose gel 1%, Migration 90V
Quantification, from left to right: 1. DNA Ladder, 2. BBa_K1707011#3 (08/12), 3. BBa_K1707011#3 (08/12), 4. BBa_K1707012#2 (08/12), 5. BBa_K1707012#2 (08/13), 6. BBa_K1707033#1, 7. BBa_K1707033#2, 8. BBa_R0051 (2nd send), 9. Empty, 10. Empty
We can conclude:- BBa_R0051 (2nd send): 13 µg/µL
- BBa_K1707011 #3: 40 µg/µL
- BBa_K1707012 #2: 35 µg/µL
- BBa_K1707033 #1 and #2: 20 µg/µL
New culture
by Pauline
- BBa_K1707035
- BBa_K1707036
We put 2 new clones in 5mL LB + 5µL Chloramphenicol
Plasmid extraction
by Pauline
- BBa_K1707031 #3, #4, #5 and #6
With Macherey-Nagel Extraction kit
Digestion
by Pauline
- BBa_K1707031 #3, #4, #5 and #6
Mix for each:
- BBa_K1707011 and BBa_K1707012
- 0,5 µL XbaI
- 0,5 µL PstI
- 1 µL FastDigest Buffer 10x
- 6 µL H2O
- 2 µL plasmid
Incubation 37°C, 1H30
Ligation
by Pauline
- BBa_K1707023: BBa_K1707012 and BBa_J23101
- 5,9 µL BBa_K1707012
- 5 µL BBa_J23101
- 2 µL Ligase
- 1,5 µL Buffer
- 0,6 µL H2O
- BBa_K1707022: BBa_K1707011 and BBa_R0051
- 5,4 µL BBa_K1707011
- 7,6 µL BBa_R0051
- 2 µL Ligase
- 2 µL Buffer
- 3 µL H2O
- BBa_K1707034: BBa_K1707033 and BBa_J23101
- 11 µL BBa_K1707033
- 5 µL BBa_J23101
- 2 µL Ligase
- 2 µL Buffer
Incubation 3h, 4°C
Electrophoresis
by Pauline
Agarose gel, 1%, Migration 90V
Verification of gel purification, from left to right: 1. DNA Ladder, 2. BBa_K1707030#3, 3. BBa_K1707031#4, 4. BBa_K1707031#5, 5. BBa_K1707031#6, 6. Empty, 7. Empty, 8. Empty, 9. Empty, 10. Empty
Biobricks:- Verification:
- BBa_K1707031 #3, #4, #5 and #6
We can conclude that all clones aren't OK because the band viewed corresponding to the BBa_R0040 plasmid
Transformation
by Pauline
- BBa_K1707022
- BBa_K1707023
- BBa_K1707034
Soil experiment
by Coralie and Johan
Low budget experiment
by Coralie
Member present:
- Instructors: Claire
- Students: Coralie and Pauline