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Team:Paris Saclay/Notebook/August/28
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==Lab Work== | ==Lab Work== | ||
| - | === | + | ===Construction of the fusion protein (color)=== |
====Transformation of DH5a by PSB1C3+chromoprotein==== | ====Transformation of DH5a by PSB1C3+chromoprotein==== | ||
| - | + | ''by Mélanie'' | |
--> a compléter | --> a compléter | ||
| Line 64: | Line 64: | ||
| - | === | + | ===lemon scent=== |
| - | ==== Electrophoresis of | + | ==== Electrophoresis of 5 digestions of pPS5 by HindIII to check if the insert of CAD is in the right position ==== |
| - | + | ||
| - | [[File:280814 HV degisetion.jpg|300px]] | + | [[File:280814 HV degisetion.jpg|300px|right]] |
| + | ''by Hoang Vu'' | ||
| + | |||
| + | 1-5: pPS5 (pJBEI+CAD) digested by HindIII | ||
| + | |||
| + | 6: pPS1 (pJBEI+Apra), our witness | ||
| + | |||
| + | 7-8: ladder | ||
====Electrophoresis of the same 5 PCR pooled==== | ====Electrophoresis of the same 5 PCR pooled==== | ||
| + | |||
| + | [[File:280814 Laetitia verif decoup.jpg|300px|left]] | ||
''by Laetitia'' | ''by Laetitia'' | ||
| Line 78: | Line 86: | ||
The totality of the 5 PCR have been used. Then, we cut the lane corresponding of the Limonene synthase gene on a UV table. | The totality of the 5 PCR have been used. Then, we cut the lane corresponding of the Limonene synthase gene on a UV table. | ||
| - | |||
====Purification of the PCR product of Limonene synthase (BBa762100)==== | ====Purification of the PCR product of Limonene synthase (BBa762100)==== | ||
| Line 84: | Line 91: | ||
We used the kit PCR-Clean-UP to extract the DNA from the agarose gel. Elution volume : 15µl | We used the kit PCR-Clean-UP to extract the DNA from the agarose gel. Elution volume : 15µl | ||
| - | |||
| + | ==Photo of the Day== | ||
| + | [[File:Paris Saclay 28_august.jpg|400px|center]] | ||
| + | '''Members present:''' | ||
| + | * Instructors and advisors: Alice, Solenne and Sylvie. | ||
| + | * Students: Eugène, Hoang Vu, Laëtitia, Mélanie, Romain, Sean and Terry. | ||
{{Team:Paris_Saclay/notebook_footer}} | {{Team:Paris_Saclay/notebook_footer}} | ||
Latest revision as of 15:28, 14 October 2014
Contents |
Thursday 28th August
Lab Work
Construction of the fusion protein (color)
Transformation of DH5a by PSB1C3+chromoprotein
by Mélanie
--> a compléter
Addition of adenines at the ends of PCR fragment of chromoprotein
by Laetitia
| components | volumes |
|---|---|
| H2O | 1 μl |
| Gotaq buffer 5X | 1µl |
| dATP 1mM | 2 µl |
| Chromoprotein gene fragment (30ng/µL) | 5µL |
| Gotaq polymerase | 1µl |
1h- 70°C
Ligation of the PCR fragment of chromoprotein + AAA with pGEMTeasy
by Laetitia
| components | volumes |
|---|---|
| 2X ligation buffer T4 DNA ligase | 10 μl |
| pGEMTeasy | 1µl |
| Ligation mix | 7 µl |
| Ligase | 2µL |
4h - 16°C
lemon scent
Electrophoresis of 5 digestions of pPS5 by HindIII to check if the insert of CAD is in the right position
by Hoang Vu
1-5: pPS5 (pJBEI+CAD) digested by HindIII
6: pPS1 (pJBEI+Apra), our witness
7-8: ladder
Electrophoresis of the same 5 PCR pooled
by Laetitia
Gel agarose 0,8% - 100V
The totality of the 5 PCR have been used. Then, we cut the lane corresponding of the Limonene synthase gene on a UV table.
Purification of the PCR product of Limonene synthase (BBa762100)
by Laetitia We used the kit PCR-Clean-UP to extract the DNA from the agarose gel. Elution volume : 15µl
Photo of the Day
Members present:
- Instructors and advisors: Alice, Solenne and Sylvie.
- Students: Eugène, Hoang Vu, Laëtitia, Mélanie, Romain, Sean and Terry.
