(→Glycerol stocks of clones X, X, X and X containing corrected dCas9 ST - GFP 11 in pSB1C3 (pPS16_017)) |
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= Friday 23<sup>rd</sup> September= | = Friday 23<sup>rd</sup> September= | ||
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===Visualization=== | ===Visualization=== | ||
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Dh5a cells were transformed with pSB1C3 containing FKBP - GFP 10 (pPS16_018), or controls (no buffer mix and plasmid alone) using the usual [[Team:Paris_Saclay/Experiments#heat-shocktransformation|protocol]]. | Dh5a cells were transformed with pSB1C3 containing FKBP - GFP 10 (pPS16_018), or controls (no buffer mix and plasmid alone) using the usual [[Team:Paris_Saclay/Experiments#heat-shocktransformation|protocol]]. | ||
− | ==== Glycerol stocks of clones | + | ==== Glycerol stocks of clones 2, 7 and 8 containing corrected dCas9 ST - GFP 11 in pSB1C3 (pPS16_017)==== |
− | + | ''By Maxence, Mahnaz & Coline'' | |
The glycerol stock of the bacteria with the following plasmids were made. | The glycerol stock of the bacteria with the following plasmids were made. | ||
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500µL of liquid culture and 250 µL of glycerol 60% were mixed and put at -20°C. | 500µL of liquid culture and 250 µL of glycerol 60% were mixed and put at -20°C. | ||
− | ====Plasmids extraction of clones | + | ====Plasmids extraction of clones 2, 7 and 8 containing corrected dCas9 ST - GFP 11 in pSB1C3 (pPS16_017)==== |
− | + | ''By Maxence, Mahnaz & Coline'' | |
The following plasmids were extracted using the [[Team:Paris_Saclay/Experiments#InvitrogenPlasmidExtraction|"Charge Switch-Pro Plasmid Miniprep"]] kit: | The following plasmids were extracted using the [[Team:Paris_Saclay/Experiments#InvitrogenPlasmidExtraction|"Charge Switch-Pro Plasmid Miniprep"]] kit: | ||
− | *pPS16_017 (dCas9 ST - GFP 11) clone | + | *pPS16_017 (dCas9 ST - GFP 11) clone 2 |
− | *pPS16_017 (dCas9 ST - GFP 11) clone | + | *pPS16_017 (dCas9 ST - GFP 11) clone 7 |
− | *pPS16_017 (dCas9 ST - GFP 11) clone | + | *pPS16_017 (dCas9 ST - GFP 11) clone 8 |
− | + | ||
− | ==== Glycerol stocks of clones | + | ==== Glycerol stocks of clones 3, 4, 7 and 8 containing GFP 1.9 in pSB1C3 (pPS16_020)==== |
− | + | ''By Maxence, Mahnaz & Coline'' | |
The glycerol stock of the bacteria with the following plasmids were made. | The glycerol stock of the bacteria with the following plasmids were made. | ||
− | *pPS16_020 (GFP 1.9) clone | + | *pPS16_020 (GFP 1.9) clone 3 |
− | *pPS16_020 (GFP 1.9) clone | + | *pPS16_020 (GFP 1.9) clone 4 |
− | *pPS16_020 (GFP 1.9) clone | + | *pPS16_020 (GFP 1.9) clone 7 |
− | *pPS16_020 (GFP 1.9) clone | + | *pPS16_020 (GFP 1.9) clone 8 |
500µL of liquid culture and 250 µL of glycerol 60% were mixed and put at -20°C. | 500µL of liquid culture and 250 µL of glycerol 60% were mixed and put at -20°C. | ||
− | ====Plasmids extraction of clones | + | ====Plasmids extraction of clones 3, 4, 7 and 8 containing GFP 1.9 in pSB1C3 (pPS16_020)==== |
− | + | ''By Maxence, Mahnaz & Coline'' | |
The following plasmids were extracted using the [[Team:Paris_Saclay/Experiments#InvitrogenPlasmidExtraction|"Charge Switch-Pro Plasmid Miniprep"]] kit: | The following plasmids were extracted using the [[Team:Paris_Saclay/Experiments#InvitrogenPlasmidExtraction|"Charge Switch-Pro Plasmid Miniprep"]] kit: | ||
− | *pPS16_020 (GFP 1.9) clone | + | *pPS16_020 (GFP 1.9) clone 3 |
− | *pPS16_020 (GFP 1.9) clone | + | *pPS16_020 (GFP 1.9) clone 4 |
− | *pPS16_020 (GFP 1.9) clone | + | *pPS16_020 (GFP 1.9) clone 7 |
− | *pPS16_020 (GFP 1.9) clone | + | *pPS16_020 (GFP 1.9) clone 8 |
{{Team:Paris_Saclay/notebook_footer}} | {{Team:Paris_Saclay/notebook_footer}} |
Latest revision as of 17:08, 9 October 2016