Measurement
=07/01:=
Rehydratation : I13504 J23117 J23106 J23101
=07/02=
Transformation : I13504 J23117 J23106 J23101
=07/03=
Liquide culture : I13504 J23117 J23106 J23101
=07/08=
==First Digestion:==
BBa_J23101
BBa_J23106
BBa_J23117
Mix:
10µL of our plasmid with promotor
1µL SpeI
1µL PstI
2µL buffer 10x FastDigest
6µL H2O
==Second Digestion:==
BBa_I13504
Mix:
10µL of our plasmid with gene
1µL XbaI
1µL PstI
2µL buffer 10x FastDigest
Incubation 1h30, 37°C
=07/09=
==Transformation:==
BBa_J23101 + BBa_I13504
BBa_J23106 + BBa_I13504
BBa_J23117 + BBa_I13504
On LB + Chloramphenicol 20ug/mL. Incubation ON, 37°C
=07/15=
==Liquid culture:==
BBa_J23101 + BBa_I13504
BBa_J23106 + BBa_I13504
BBa_J23117 + BBa_I13504
We can observe from the plate that BBa_J23101 + BBa_I13504 and BBa_J23106 + BBa_I13504 are yellow when we expose them to the UV light. But BBa_J23117 + BBa_I13504 don't seem to be yellow on the UV light.
=07/16=
==Digestion:==
BBa_J23101 + BBa_I13504
BBa_J23106 + BBa_I13504
BBa_J23117 + BBa_I13504
==Reaction mix:==
Plasmid: 2µL
EcoRI: 0,5µL
PstI: 0,5µL
Buffer FastDigest (10x): 2µL
H2O: 15µL
==Electrophoresis:==
Preparation of Agarose Gel 1%, 0,5g in 50mL of 1X TAE, 0,5µL of BET Migration 0,06A 80V
[[File:ParisSaclay_16.07.15_-_digestion_vérif.jpg|thumb|none]]
=07/17=
==New culture on Plate==
BBa_J23101 + BBa_I13504
BBa_J23106 + BBa_I13504
BBa_J23117 + BBa_I13504
=07/23=
Liquid culture from the 3 stocks
=07/24=
==Cytometer==
We count 500 000 events Controls:
Cells alones
Cells transformed by BBa_J23101, BBa_J23106 and BBa_J23117
Our measurements: Cells transformed by
BBa_J23101 + BBa_I13504
BBa_J23106 + BBa_I13504
BBa_J23117 + BBa_I13504
We uses cells in growth phase and stationary phase
Between each test, we do 2 washes with bleach and 2 washes with H2O
=07/28=
New culture of BBa_J23101/BBa_J23106/BBa_J23117 + BBa_I13504
==Tecan utilisation:==
we use only LB without chloramphenicol and we suspect a contamination of our samples.
We depose in inch well 300µL
We analyse the OD and fluorescence's variation (the excitation and emission wave lenght were choose after a scan in the process to obtain the best results)
For each sample, we depose twelve time (12x8 plate)
*LB
*Competent cells
*Cells with J23101
*Cells with J23101 + GFP
*Cells with J23106
*Cells with J23106 + GFP
*Cells with J23117
*Cells with J23117 + GFP
We let's run for 20 cycles of 1 hour
.=07/29=
==Tecan utilisation:==
This time, we use LB and chloramphenicol because the plate has just a protection and we suspect a contamination of our samples.
We depose in inch well 300µL
We analyse the OD and fluorescence's variation (the excitation and emission wave lenght were choose after a scan in the process to obtain the best results)
For each sample we use 3 different colonies, we depose 2 times each colonies (12x8 plate)
LB
Competent cells
Cells with J23101
Cells with J23101 + GFP
Cells with J23106
Cells with J23106 + GFP
Cells with J23117
Cells with J23117 + GFP
We let's run for 20 cycles of 1 hour
==Flow cytometer==
We analyse the sample see previously with ODmax and OD 0.4 But we doesn't use the good scale so we will reused it tomorrow
=07/30=
==Flow cytometer==
We count 500 000 events Controls:
LB
Cells transformed by BBa_J23101, BBa_J23106 and BBa_J23117
Our measurements: Cells transformed by
BBa_J23101 + BBa_I13504
BBa_J23106 + BBa_I13504
BBa_J23117 + BBa_I13504
We uses cells in growth phase and stationary phase
Between each test, we do 2 washes with bleach and 2 washes with H2O
We use a less powerful adjustment to see tall the result than the day before.