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Team:DTU-Denmark/Notebook/3 July 2013
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| + | {{:Team:DTU-Denmark/Templates/StartPage|3 July 2013}} | ||
| + | Navigate to the [[Team:DTU-Denmark/Notebook/2_July_2013|Previous]] or the [[Team:DTU-Denmark/Notebook/4_July_2013|Next]] Entry | ||
=208 lab= | =208 lab= | ||
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== Main purposes today == | == Main purposes today == | ||
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Verify insert plated made Sunday. Run BioLector experiment. | Verify insert plated made Sunday. Run BioLector experiment. | ||
==who were in the lab== | ==who were in the lab== | ||
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Kristian, Ariadni | Kristian, Ariadni | ||
==Procedure== | ==Procedure== | ||
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Gel on colony PCR from yesterday. | Gel on colony PCR from yesterday. | ||
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==Results== | ==Results== | ||
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[[File:03.07.13 Colony PCR.jpg|thumb|left|The gel from colony PCR. From left to right; Sec1, Sec2, Sec3, TAT2 1, TAT2 2, TAT2 3, TAT3 1, TAT3 2, TAT3 3, TAT3 1a, TAT3 2a. Where the different TATs are either with(TAT2) or without insertion of 2 additional amino acids to ease the primer design. 1kb plus ladder([http://www.invitrogen.com/site/us/en/home/Products-and-Services/Applications/DNA-RNA-Purification-Analysis/Nucleic-Acid-Gel-Electrophoresis/DNA-Ladders/Track-IT-Ladders.html invitrogen]) ]] | [[File:03.07.13 Colony PCR.jpg|thumb|left|The gel from colony PCR. From left to right; Sec1, Sec2, Sec3, TAT2 1, TAT2 2, TAT2 3, TAT3 1, TAT3 2, TAT3 3, TAT3 1a, TAT3 2a. Where the different TATs are either with(TAT2) or without insertion of 2 additional amino acids to ease the primer design. 1kb plus ladder([http://www.invitrogen.com/site/us/en/home/Products-and-Services/Applications/DNA-RNA-Purification-Analysis/Nucleic-Acid-Gel-Electrophoresis/DNA-Ladders/Track-IT-Ladders.html invitrogen]) ]] | ||
No results from restriction analysis because we saw no bands on the gel. We assume that this is caused by the low DNA concentration. | No results from restriction analysis because we saw no bands on the gel. We assume that this is caused by the low DNA concentration. | ||
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== Conclusion from today == | == Conclusion from today == | ||
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TAT2 1 and TAT3 1a have the right bands on colony PCR and will be further analyzed. | TAT2 1 and TAT3 1a have the right bands on colony PCR and will be further analyzed. | ||
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| + | Navigate to the [[Team:DTU-Denmark/Notebook/2_July_2013|Previous]] or the [[Team:DTU-Denmark/Notebook/4_July_2013|Next]] Entry | ||
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| + | {{:Team:DTU-Denmark/Templates/EndPage}} | ||
Latest revision as of 20:38, 16 September 2013
3 July 2013
Contents |
208 lab
Main purposes today
Verify insert plated made Sunday. Run BioLector experiment.
who were in the lab
Kristian, Ariadni
Procedure
Gel on colony PCR from yesterday.
Setup of BioLector experiment.
MiniPrep selected colonies and make restriction digest analysis.
Results
No results from restriction analysis because we saw no bands on the gel. We assume that this is caused by the low DNA concentration.
Conclusion from today
TAT2 1 and TAT3 1a have the right bands on colony PCR and will be further analyzed.
Navigate to the Previous or the Next Entry
