Difference between revisions of "Team:Paris Saclay/Notebook/July/30"

(Electrophoresis)
 
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Agarose gel 1%, migration 80V then 110V
 
Agarose gel 1%, migration 80V then 110V
 
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[[File:ParisSaclay 30.07.15-vérification plasmides.jpg|300px|center]]
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<html><i><p>Verification by digestion with XbaI, from left to right: 1. <a href="https://2015.igem.org/File:Paris_Saclay-Ladder.jpg" target="_blank">DNA Ladder</a>, 2. BBa_J23101, 3. BBa_K1707008#2, 4. BBa_K1707008#3, 5. BBa_K1707008#4, 6. BBa_K1707008#5, 7. BBa_K1707008#6, 8. BBa_K1707001#1, 9. BBa_K1707005#1, 10. BBa_K1707005#2, 11. Empty, 12. Empty</p></i></html>
 
We can conclude that BBa_K1707008 isn't OK, and BBa_K1707005 #1 and #2 are OK
 
We can conclude that BBa_K1707008 isn't OK, and BBa_K1707005 #1 and #2 are OK
  
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''by Johan''
 
''by Johan''
  
We count 500 000 events
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https://2015.igem.org/Team:Paris_Saclay/Measurement#30th_July
Controls:
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* Cells alones
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* Cells transformed by BBa_J23101, BBa_J23106 and BBa_J23117
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Our measurements: Cells transformed by
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* BBa_J23101 + BBa_I13504
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* BBa_J23106 + BBa_I13504
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* BBa_J23117 + BBa_I13504
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We uses cells in growth phase and stationary phase
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Between each test, we do 2 washes with bleach and 2 washes with H2O
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We use a less powerful adjustment to see tall the result than the day before.
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'''Member present:'''
 
'''Member present:'''

Latest revision as of 21:25, 18 September 2015


Thursday 30th July

Lab Work

Transformation

by Audrey

Biobricks:

  • BBa_K1707004
  • BBa_K1707009

As usual


Plasmid extraction

by Johan

Biobricks:

  • BBa_K1707008 #3, #4, #5 and #6

With the Macherey-Nagel Extraction kit


Ligation

by Pauline

  • BBa_K1707011: BBa_B0030 + BBa_K1707010 #1
    • 3 µL BBa_B0030
    • 5 µL BBa_K1707010
    • 2 µL Buffer Ligase 10x
    • 1 µL Ligase


  • BBa_K1707021: BBa_K1707000 + BBa_K1707010
    • 1,5µL BBa_K1707000
    • 5 µL BBa_K1707006
    • 1 µL Buffer Ligase 10x
    • 1 µL Ligase
    • 1,5 µL H2O

Incubation 4h, 4°C


Digestion Verification

by Pauline

  • Biobricks:
    • BBa_K1707008 #2, #3, #4, #5, #6
    • BBa_K1707005 #1 and #2
  • Mix:
    • 1 µL Buffer FastDigest 10x
    • 0,5 µL XbaI
    • 2 µL Plasmid
    • 6,5 µL H2O

Incubation 1h30, 37°C


Electrophoresis

by Pauline

Agarose gel 1%, migration 80V then 110V

ParisSaclay 30.07.15-vérification plasmides.jpg

Verification by digestion with XbaI, from left to right: 1. DNA Ladder, 2. BBa_J23101, 3. BBa_K1707008#2, 4. BBa_K1707008#3, 5. BBa_K1707008#4, 6. BBa_K1707008#5, 7. BBa_K1707008#6, 8. BBa_K1707001#1, 9. BBa_K1707005#1, 10. BBa_K1707005#2, 11. Empty, 12. Empty

We can conclude that BBa_K1707008 isn't OK, and BBa_K1707005 #1 and #2 are OK

New Culture

by Pauline

Biobricks:

  • BBa_K1707012
  • BBa_K1707013
  • BBa_K1707019

4 clones for each, in 5ML LB + 20 ng/µL Chloramphenicol

Transformation

by Johan and Pauline

Biobricks:

  • BBa_K1707021
  • BBa_K1707011
  • BBa_I13600

As usual

Ligation

by Coralie

  • BBa_K1707008: BBa_J23101 + BBa_K1707003
    • 2,5 µL BBa_J23101
    • 11 µL BBa_K1707003
    • 2 µL Buffer Ligase 10x
    • 1 µL Ligase
    • 3,5 µL H2O

Incubation over night, 16°C


Soil experiment

by Coralie

Soil

Observation of J0 plates: there are a lot of colony in each. Contamination is alright. Controls (+) and (-) are Ok too. We take 1g of each pot of soil and we dilute it in 5mL sterile H2O. After shaking and decant, we put 100µL of supernatant on the right plate. Incubation ON 37°C

Interlab study: Cytometer

by Johan

https://2015.igem.org/Team:Paris_Saclay/Measurement#30th_July

Member present:

  • Instructors: Alice
  • Students: Coralie, Audrey, Pauline, Johan and Seong-Koo

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