Difference between revisions of "Team:Paris Saclay/Notebook/July/23"
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{{Team:Paris_Saclay/notebook_header}} | {{Team:Paris_Saclay/notebook_header}} | ||
− | =Thursday | + | =Thursday 23th July= |
==Lab Work== | ==Lab Work== | ||
===Soil experiment=== | ===Soil experiment=== | ||
Line 52: | Line 52: | ||
Migration 80V | Migration 80V | ||
Biobricks: BBa_K1707003 #4 to #9 digested by EcoRI or EcoRI+PstI | Biobricks: BBa_K1707003 #4 to #9 digested by EcoRI or EcoRI+PstI | ||
− | + | [[File:Paris Saclay-23.07.2015 plasmides 2.jpg|300px|center]] | |
− | We can't conclude anything because we | + | <html><p><i>Verification by digestion with EcoRI of BBa_K1707003, from left to right: 1. <a href="https://2015.igem.org/File:Paris_Saclay-Ladder.jpg" target="_blank">DNA Ladder</a>, 2. #4 digested by EcorRI and PstI, 3. #5, 4. #6, 5.#7, 6. #8, 7. #9, 8. Empty, 9. Empty, 10. Empty</i></p></html> |
+ | [[File:Paris Saclay-23.07.2015 plasmides 1.jpg|300px|center]] | ||
+ | <html><p><i>Verification by digestion with EcoRI and PstI of BBa_K1707003, from left to right: 1. <a href="https://2015.igem.org/File:Paris_Saclay-Ladder.jpg" target="_blank">DNA Ladder</a>, 2. #4 digested by EcorRI, 3. #5, 4. #6, 5.#7, 6. #8, 7. #9, 8. Empty, 9. Empty, 10. Empty</i></p></html> | ||
+ | We can't conclude anything because we inverted #4 in each gel and we forgot the control | ||
===Digestion=== | ===Digestion=== | ||
Line 83: | Line 86: | ||
Migration 80V | Migration 80V | ||
Biobricks: BBa_K1707003 #4 and #5 and BBa_B0015 digested by EcoRI or EcoRI+PstI | Biobricks: BBa_K1707003 #4 and #5 and BBa_B0015 digested by EcoRI or EcoRI+PstI | ||
− | + | [[File:Paris Saclay-23.07.2015 plasmides final.jpg|300px|center]] | |
+ | <html><p><i>Verification by digestion of BBa_K1707003, from left to right: 1. <a href="https://2015.igem.org/File:Paris_Saclay-Ladder.jpg" target="_blank">DNA Ladder</a>, 2. #4 digested by EcorRI, 3. #5 digested by EcorRI, 4. Indicator, 5.#4 digested by EcorRI and PstI, 6. #5 digested by EcorRI and PstI, 7. Indicator, 8. Empty, 9. Empty, 10. Empty</i></p></html> | ||
We can confirm the BBa_K1707003 #4 and #5 | We can confirm the BBa_K1707003 #4 and #5 | ||
Line 96: | Line 100: | ||
Agarose gel 1%, migration 70V | Agarose gel 1%, migration 70V | ||
− | + | [[File:ParisSaclay 23.07.2015 Purification.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_K1707002, 3. BBa_K098997, 4. BBa_C0040</i></p></html> | ||
We cut bands with a scalpel | We cut bands with a scalpel | ||
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Agarose gel 1% | Agarose gel 1% | ||
Migration 110V | Migration 110V | ||
− | + | [[File:Paris Saclay-23.07.2015 quantif.jpg|300px|center]] | |
+ | <html><p><i>Wells 2-6: Quantification, Well 7: Verification; from left to right: 1. <a href="https://2015.igem.org/File:Paris_Saclay-Ladder.jpg" target="_blank">DNA Ladder</a>, 2. BBa_K098997, 3. BBa_B0015, 4. BBa_C0051, 5. BBa_K1707002, 6. BBa_K1707001, 7. K1707000 plasmid, 8. Empty, 9. Empty, 10. Empty, 11. Empty, 12. Empty</i></p></html> | ||
We can conclude that the BBa_K1707000 PCR is ok. So the biobrick is confirmed | We can conclude that the BBa_K1707000 PCR is ok. So the biobrick is confirmed | ||
Line 159: | Line 165: | ||
'''Member present:''' | '''Member present:''' | ||
* Instructors:Alice | * Instructors:Alice | ||
− | * Students: Audrey, Coralie, Pauline, Seong | + | * Students: Audrey, Coralie, Pauline, Seong Koo, Johan |
{{Team:Paris_Saclay/notebook_footer}} | {{Team:Paris_Saclay/notebook_footer}} |
Latest revision as of 21:18, 18 September 2015
Contents
Thursday 23th July
Lab Work
Soil experiment
by Audrey, Seong Koo and Johan
Plates observation and count of CFU:
- Strain 1696:
- Dilution 1: 490 CFU
- Dilution 0.1: 67 CFU
- Dilution 0.01: 0 CFU
- Strain 1693:
- Dilution 1: 1308 CFU
- Dilution 0.1: 196 CFU
- Dilution 0.01: 0 CFU
- Strain 1320:
- Dilution 1: 186 CFU
- Dilution 0.1: 35 CFU
- Dilution 0.01: 1 CFU
We take 1g of contaminated soil and treat it like yesterday to spread it on specific plates Incubation ON, 37°C
Digestion
by Coralie
Biobrick: BBa_K1707003 #4 to #9
- Digestion by EcoRI: mix
- 6µL EcoRI
- 6µL Buffer FastDigest 10x
- 36µL H2O
We put 8µL of the mix in each tube + 2µL of our plasmids
- Digestion by EcoRI + PstI: mix
- 6µL EcoRI
- 6µL PstI
- 6µL Buffer FastDigest 10x
- 30µL H2O
We put 8µL of the mix in each tube + 2µL of our plasmids
Incubation 1h30, 37°C
Electrophoresis
by Johan
Agarose gel: 1% Migration 80V Biobricks: BBa_K1707003 #4 to #9 digested by EcoRI or EcoRI+PstI
Verification by digestion with EcoRI of BBa_K1707003, from left to right: 1. DNA Ladder, 2. #4 digested by EcorRI and PstI, 3. #5, 4. #6, 5.#7, 6. #8, 7. #9, 8. Empty, 9. Empty, 10. Empty
Verification by digestion with EcoRI and PstI of BBa_K1707003, from left to right: 1. DNA Ladder, 2. #4 digested by EcorRI, 3. #5, 4. #6, 5.#7, 6. #8, 7. #9, 8. Empty, 9. Empty, 10. Empty
We can't conclude anything because we inverted #4 in each gel and we forgot the controlDigestion
by Coralie
Biobricks: BBa_K1707003 #4 and #5 and BBa_B0015
- Digestion by EcoRI: mix
- 3µL EcoRI
- 3µL Buffer FastDigest 10x
- 18µL H2O
We put 8µL of the mix in each tube + 2µL of our plasmids
- Digestion by EcoRI + PstI: mix
- 3µL EcoRI
- 3µL PstI
- 3µL Buffer FastDigest 10x
- 15µL H2O
We put 8µL of the mix in each tube + 2µL of our plasmids
Incubation 1h30, 37°C
Electrophoresis
by Coralie
Agarose gel: 1% Migration 80V Biobricks: BBa_K1707003 #4 and #5 and BBa_B0015 digested by EcoRI or EcoRI+PstI
Verification by digestion of BBa_K1707003, from left to right: 1. DNA Ladder, 2. #4 digested by EcorRI, 3. #5 digested by EcorRI, 4. Indicator, 5.#4 digested by EcorRI and PstI, 6. #5 digested by EcorRI and PstI, 7. Indicator, 8. Empty, 9. Empty, 10. Empty
We can confirm the BBa_K1707003 #4 and #5
Gel purification
by Audrey
Biobricks:
- BBa_K1707002
- BBa_K098997
- BBa_C0051
Agarose gel 1%, migration 70V
Verification of gel purification, from left to right: 1. DNA Ladder, 2. BBa_K1707002, 3. BBa_K098997, 4. BBa_C0040
We cut bands with a scalpelPurification
by Audrey
Biobricks:
- BBa_K098997
- BBa_B0015
- BBa_C0051
- BBa_K1707002
- BBa_K1707001
With PCR Clean up/Gel extraction kit from Macherey Nigel
Quantification and Verification
by Audrey
Biobricks:
- Quantification:
- BBa_K098997
- BBa_B0015
- BBa_C0051
- BBa_K1707002
- BBa_K1707001
- Verification:
- BBa_K1707000
Agarose gel 1% Migration 110V
Wells 2-6: Quantification, Well 7: Verification; from left to right: 1. DNA Ladder, 2. BBa_K098997, 3. BBa_B0015, 4. BBa_C0051, 5. BBa_K1707002, 6. BBa_K1707001, 7. K1707000 plasmid, 8. Empty, 9. Empty, 10. Empty, 11. Empty, 12. Empty
We can conclude that the BBa_K1707000 PCR is ok. So the biobrick is confirmedLigation
by Coralie
- BBa_K1707006
- 3µL BBa_C0051
- 2µL BBa_B0015
- 1µL Ligase
- 1µL Buffer 10x
- 3µL H2O
- BBa_K1707007
- 8µL BBa_K098997
- 2µL BBa_B0015
- 1µL Ligase
- 2µL Buffer 10x
- 7µL H2O
- BBa_K1707005
- 13µL BBa_K1707002
- 2µL BBa_K1707001
- 1µL Ligase
- 2µL Buffer 10x
- 2µL H2O
Incubation ON, 4°C
Member present:
- Instructors:Alice
- Students: Audrey, Coralie, Pauline, Seong Koo, Johan