Team:Paris-Saclay/Project/Notebook/Week 11

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{{Team:Paris-Saclay/Follow}}
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='''Week 11'''=
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[[Category:Team:Paris-Saclay/Project Gemote/Notebook|5]]
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[[Category:Team:Paris-Saclay/Project Gemote/Notebook|k]]
__NOTOC__
__NOTOC__
====13th August====
====13th August====
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|-
|-
| style="width: 50%;"|Purification by PCR clean-up of BBa_K115017 treated with DPNI. To visualize the fragment, an electrophoresis has been made with a 2% Agarose gel. We are expecting a band at the size of 123 bp.
| style="width: 50%;"|Purification by PCR clean-up of BBa_K115017 treated with DPNI. To visualize the fragment, an electrophoresis has been made with a 2% Agarose gel. We are expecting a band at the size of 123 bp.
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| style="width: 35%;"| [[File:Week11-1.jpg|right|330px]]
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| style="width: 35%;"| [[File:Week11-1.jpg|right|280px]]
|-
|-
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| style="width: 50%;"|[[File:Week11-2.jpg|left|330px]]
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| style="width: 50%;"|[[File:Week11-2.jpg|left|280px]]
| style="width: 35%;"| New PCR of BBa_K115017 to obtain more quantity of the fragment
| style="width: 35%;"| New PCR of BBa_K115017 to obtain more quantity of the fragment
|}
|}
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PCR program used:
PCR program used:
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[[File:Week11-3.jpg|600px]]
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[[File:Week11-3.jpg|500px]]
*Digestion by DPNI of the BBa_K115017 in order to degrade the matrix plasmid.
*Digestion by DPNI of the BBa_K115017 in order to degrade the matrix plasmid.
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{| width="85%"
{| width="85%"
|-
|-
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| style="width: 50%;"|Determining the concentration of the plasmid pSB1A2 which has been linearized by HINDIII. We are expecting a band at the size of (2079+935) ~3kbp
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| style="width: 50%;"|Determination of the concentration of plasmid pSB1A2 which has been linearized by HINDIII. We are expecting a band at size (2079+935) ~3kbp
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| style="width: 35%;"| [[File:Week11-4.jpg|right|330px]]
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| style="width: 35%;"| [[File:Week11-4.jpg|right|280px]]
|-
|-
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| style="width: 50%;"|A new PCR of the plasmid pSB1A2 is realized to obtain more quantity of the plasmid. We are expecting a band at the size of 2079 bp.
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| style="width: 50%;"|A new PCR of the plasmid pSB1A2 is realized to obtain more quantity of the plasmid. We are expecting a band at size 2079 bp.
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| style="width: 35%;"| [[File:Week11-5.jpg|right|330px]]
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| style="width: 35%;"| [[File:Week11-5.jpg|right|280px]]
|}
|}
PCR program used:
PCR program used:
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[[File:Week11-6.jpg|600px]]
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[[File:Week11-6.jpg|500px]]
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====14th August====
====14th August====
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{| width="85%"
{| width="85%"
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|-
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| style="width: 50%;"|Determining of the concentration of the BBa_K274100 by electrophoresis on a gel at O.8% Agarose. We are expecting a band at the size of 2100bp
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| style="width: 50%;"|Determination of the concentration of the BBa_K274100 by electrophoresis on a gel at O.8% Agarose. We are expecting a band at size 2100bp
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| style="width: 35%;"| [[File:Week11-7.jpg|right|330px]]
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| style="width: 35%;"| [[File:Week11-7.jpg|right|280px]]
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**PSB1A3Amil CP + Ampicilline
**PSB1A3Amil CP + Ampicilline
**PSB1C3 Amil GFP + Chloramphinicol
**PSB1C3 Amil GFP + Chloramphinicol
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====15th August====
====15th August====
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Day of public holiday in France.
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French holiday.
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====16th August====
====16th August====
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|-
|-
| style="width: 50%;"|PCR of BBa_K274100 and visualization by 0.8% Agarose gel electrophoresis. We are expecting a band at 3400bp.
| style="width: 50%;"|PCR of BBa_K274100 and visualization by 0.8% Agarose gel electrophoresis. We are expecting a band at 3400bp.
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| style="width: 35%;"| [[File:Week11-8.jpg|right|330px]]
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| style="width: 35%;"| [[File:Week11-8.jpg|right|280px]]
|}
|}
PCR program used:
PCR program used:
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[[File:Week11-9.jpg|600px]]
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[[File:Week11-9.jpg|500px]]
*Digestion of the BBa_K274100 by DPNI to degrade the matrix plasmid.
*Digestion of the BBa_K274100 by DPNI to degrade the matrix plasmid.
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{| width="85%"
{| width="85%"
|-
|-
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| style="width: 50%;"|Visualization of the DPNI’s digestion of the plasmid pSB1A2 by 0.8% Agarose gel electrophoresis. . We are expecting a band at the size of 2079 bp.
+
| style="width: 50%;"|Visualization of the DPNI’s digestion of the plasmid pSB1A2 by 0.8% Agarose gel electrophoresis. . We are expecting a band at size 2079 bp.
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| style="width: 35%;"| [[File:Week11-10.jpg|right|330px]]
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| style="width: 35%;"| [[File:Week11-10.jpg|right|220px]]
|}
|}
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*Miniprep of the plasmid pSB1A2.
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*Miniprep of the pSB1A2 plasmid.
*Miniprep of BBa_K274100 and BBa_K115017
*Miniprep of BBa_K274100 and BBa_K115017
*Gibson assembly of the B construction
*Gibson assembly of the B construction
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Latest revision as of 00:39, 27 September 2012

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Week 11

13th August

Purification by PCR clean-up of BBa_K115017 treated with DPNI. To visualize the fragment, an electrophoresis has been made with a 2% Agarose gel. We are expecting a band at the size of 123 bp.
Week11-1.jpg
Week11-2.jpg
 New PCR of BBa_K115017 to obtain more quantity of the fragment


PCR program used: Week11-3.jpg

  • Digestion by DPNI of the BBa_K115017 in order to degrade the matrix plasmid.
Determination of the concentration of plasmid pSB1A2 which has been linearized by HINDIII. We are expecting a band at size (2079+935) ~3kbp
Week11-4.jpg
A new PCR of the plasmid pSB1A2 is realized to obtain more quantity of the plasmid. We are expecting a band at size 2079 bp.
Week11-5.jpg

PCR program used: Week11-6.jpg

14th August

Determination of the concentration of the BBa_K274100 by electrophoresis on a gel at O.8% Agarose. We are expecting a band at size 2100bp
Week11-7.jpg
  • Digestion of the BBa_K274100 by DPNI to degrade the matrix plasmid.
  • Stocking up cells with glycerol
    • PSB1A3Amil CP + Ampicilline
    • PSB1C3 Amil GFP + Chloramphinicol

15th August

French holiday.

16th August

PCR of BBa_K274100 and visualization by 0.8% Agarose gel electrophoresis. We are expecting a band at 3400bp.
Week11-8.jpg

PCR program used: Week11-9.jpg

  • Digestion of the BBa_K274100 by DPNI to degrade the matrix plasmid.

17th august

Visualization of the DPNI’s digestion of the plasmid pSB1A2 by 0.8% Agarose gel electrophoresis. . We are expecting a band at size 2079 bp.
Week11-10.jpg
  • Miniprep of the pSB1A2 plasmid.
  • Miniprep of BBa_K274100 and BBa_K115017
  • Gibson assembly of the B construction
  • Transformation of DH5α competent cells with the Gibson B construction. The Petri dishes are placed at 37°C.

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