Team:Paris Saclay/Notebook/August/6

From 2013.igem.org

(Difference between revisions)
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==='''A - Aerobic/Anaerobic regulation system'''===
==='''A - Aerobic/Anaerobic regulation system'''===
-
===='''Objective : obtaining Bba_K1155004, Bba_K1155005, Bba_K1155006'''====
+
===='''Objective : obtaining BBa_K1155004, BBa_K1155005, BBa_K1155006'''====
-
====1 - Electrophoresis to check the Colony PCR products : Bba_K1155004, Bba_K1155005, Bba_K1155006====
+
====1 - Electrophoresis to check the Colony PCR products : BBa_K1155004, BBa_K1155005, BBa_K1155006====
XiaoJing, Damir, Anaïs
XiaoJing, Damir, Anaïs
-
* Bba_K1155004 :
+
* BBa_K1155004 :
{|
{|
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| style="width:350px;border:1px solid black;vertical-align:top;" |
| style="width:350px;border:1px solid black;vertical-align:top;" |
* Well 1 : 6µL DNA Ladder
* Well 1 : 6µL DNA Ladder
-
* Well 2 to 7 : 10µL Bba_K1155004+2µl of 6X loading dye
+
* Well 2 to 7 : 10µL BBa_K1155004+2µl of 6X loading dye
* Well 8 : 6µL DNA Ladder
* Well 8 : 6µL DNA Ladder
-
* Well 9 to 14 : 10µL Bba_K1155004+2µl of 6X loading dye
+
* Well 9 to 14 : 10µL BBa_K1155004+2µl of 6X loading dye
* Well 15 : 6µL DNA Ladder
* Well 15 : 6µL DNA Ladder
* Well 16 : 6µL DNA Ladder
* Well 16 : 6µL DNA Ladder
-
* Well 17 to 22 : 10µL Bba_K1155004+2µl of 6X loading dye
+
* Well 17 to 22 : 10µL BBa_K1155004+2µl of 6X loading dye
* Well 23 : 6µL DNA Ladder
* Well 23 : 6µL DNA Ladder
-
* Well 24 to 30 : 10µL Bba_K1155004+2µl of 6X loading dye
+
* Well 24 to 30 : 10µL BBa_K1155004+2µl of 6X loading dye
* Well 31 : 6µL DNA Ladder
* Well 31 : 6µL DNA Ladder
* Gel : 1%
* Gel : 1%
|}
|}
-
*Bba_K1155005 :
+
*BBa_K1155005 :
{|
{|
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| style="width:350px;border:1px solid black;vertical-align:top;" |
| style="width:350px;border:1px solid black;vertical-align:top;" |
* Well 1 : 6µL DNA Ladder
* Well 1 : 6µL DNA Ladder
-
* Well 2 to 7 : 10µL Bba_K1155005+2µl of 6X loading dye
+
* Well 2 to 7 : 10µL BBa_K1155005+2µl of 6X loading dye
* Well 8 : 6µL DNA Ladder
* Well 8 : 6µL DNA Ladder
-
* Well 9 to 14 : 10µL Bba_K1155005+2µl of 6X loading dye
+
* Well 9 to 14 : 10µL BBa_K1155005+2µl of 6X loading dye
* Well 15 : 6µL DNA Ladder
* Well 15 : 6µL DNA Ladder
* Well 16 : 6µL DNA Ladder
* Well 16 : 6µL DNA Ladder
-
* Well 17 to 22 : 10µL Bba_K1155005+2µl of 6X loading dye
+
* Well 17 to 22 : 10µL BBa_K1155005+2µl of 6X loading dye
* Well 23 : 6µL DNA Ladder
* Well 23 : 6µL DNA Ladder
-
* Well 24 to 30 : 10µL Bba_K1155005+2µl of 6X loading dye
+
* Well 24 to 30 : 10µL BBa_K1155005+2µl of 6X loading dye
* Well 31 : 6µL DNA Ladder
* Well 31 : 6µL DNA Ladder
* Gel : 1%
* Gel : 1%
|}
|}
-
*Bba_K1155006 :
+
*BBa_K1155006 :
{|
{|
| style="width:350px;border:1px solid black;" |[[]]
| style="width:350px;border:1px solid black;" |[[]]
| style="width:350px;border:1px solid black;vertical-align:top;" |
| style="width:350px;border:1px solid black;vertical-align:top;" |
-
* Well 1 to 12 : 10µL Bba_K1155006+2µl of 6X loading dye  
+
* Well 1 to 12 : 10µL BBa_K1155006+2µl of 6X loading dye  
* Well 13 : 6µL DNA Ladder
* Well 13 : 6µL DNA Ladder
-
* Well 14 to 26 : 10µL Bba_K1155006+2µl of 6X loading dye  
+
* Well 14 to 26 : 10µL BBa_K1155006+2µl of 6X loading dye  
* Gel : 1%
* Gel : 1%
|}
|}
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{|
{|
| style="border:1px solid black;padding:5px;background-color:#DEDEDE;" |
| style="border:1px solid black;padding:5px;background-color:#DEDEDE;" |
-
We obtain fragments at the good size for all the colony. We will make a culture of DH5α with Bba_K1155004, Bba_K1155005 and Bba_K1155006. We will also sequence our plasmids.
+
We obtain fragments at the good size for all the colony. We will make a culture of DH5α with BBa_K1155004, BBa_K1155005 and BBa_K1155006. We will also sequence our plasmids.
|}
|}
-
====2 - Liquid culture of DH5α with Bba_K1155004, Bba_K1155005 and Bba_K1155006 ====
+
====2 - Liquid culture of DH5α with BBa_K1155004, BBa_K1155005 and BBa_K1155006 ====
Xiaoing, Anaïs
Xiaoing, Anaïs
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* LB : 5mL  
* LB : 5mL  
* Chloramphénicol (1000X, 20µg/mL) : 5µL
* Chloramphénicol (1000X, 20µg/mL) : 5µL
-
* Bba_K1155004, Bba_K1155005 and Bba_K1155006 : 25µL
+
* BBa_K1155004, BBa_K1155005 and BBa_K1155006 : 25µL
We let the incubation over night at 37°C at 180 RPM.
We let the incubation over night at 37°C at 180 RPM.
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We used colonies number 6, 7 and 8 for each promotor.
We used colonies number 6, 7 and 8 for each promotor.
-
===='''Objective : obtaining Bba_K1155007'''====
+
===='''Objective : obtaining BBa_K1155007'''====
-
====1 - Electroelution of Bba_I732017 digested by EcoRI/SpeI====
+
====1 - Electroelution of BBa_I732017 digested by EcoRI/SpeI====
Nadia
Nadia
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===='''Objective : obtaining biobricks in PSB3K3'''====
===='''Objective : obtaining biobricks in PSB3K3'''====
-
====1 - Extraction of Bba_J04450 from DH5α====
+
====1 - Extraction of BBa_J04450 from DH5α====
Abdou
Abdou
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==='''B - PCB sensing system'''===
==='''B - PCB sensing system'''===
-
===='''Objective : obtaining Bba_K1155002'''====
+
===='''Objective : obtaining BBa_K1155002'''====
-
====1 - Sequence analysis for Bba_K1155002 in clones 4, 17 and 22====
+
====1 - Sequence analysis for BBa_K1155002 in clones 4, 17 and 22====
{|
{|
| style="border:1px solid black;padding:5px;background-color:#DEDEDE;" |
| style="border:1px solid black;padding:5px;background-color:#DEDEDE;" |
-
The sequence is good for each clone. We obtain a new biobrick : Bba_K1155002.  
+
The sequence is good for each clone. We obtain a new biobrick : BBa_K1155002.  
|}
|}

Revision as of 09:25, 30 September 2013

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Contents

Notebook : August 6

Lab work

A - Aerobic/Anaerobic regulation system

Objective : obtaining BBa_K1155004, BBa_K1155005, BBa_K1155006

1 - Electrophoresis to check the Colony PCR products : BBa_K1155004, BBa_K1155005, BBa_K1155006

XiaoJing, Damir, Anaïs

  • BBa_K1155004 :
[[]]
  • Well 1 : 6µL DNA Ladder
  • Well 2 to 7 : 10µL BBa_K1155004+2µl of 6X loading dye
  • Well 8 : 6µL DNA Ladder
  • Well 9 to 14 : 10µL BBa_K1155004+2µl of 6X loading dye
  • Well 15 : 6µL DNA Ladder
  • Well 16 : 6µL DNA Ladder
  • Well 17 to 22 : 10µL BBa_K1155004+2µl of 6X loading dye
  • Well 23 : 6µL DNA Ladder
  • Well 24 to 30 : 10µL BBa_K1155004+2µl of 6X loading dye
  • Well 31 : 6µL DNA Ladder
  • Gel : 1%
  • BBa_K1155005 :
[[]]
  • Well 1 : 6µL DNA Ladder
  • Well 2 to 7 : 10µL BBa_K1155005+2µl of 6X loading dye
  • Well 8 : 6µL DNA Ladder
  • Well 9 to 14 : 10µL BBa_K1155005+2µl of 6X loading dye
  • Well 15 : 6µL DNA Ladder
  • Well 16 : 6µL DNA Ladder
  • Well 17 to 22 : 10µL BBa_K1155005+2µl of 6X loading dye
  • Well 23 : 6µL DNA Ladder
  • Well 24 to 30 : 10µL BBa_K1155005+2µl of 6X loading dye
  • Well 31 : 6µL DNA Ladder
  • Gel : 1%
  • BBa_K1155006 :
[[]]
  • Well 1 to 12 : 10µL BBa_K1155006+2µl of 6X loading dye
  • Well 13 : 6µL DNA Ladder
  • Well 14 to 26 : 10µL BBa_K1155006+2µl of 6X loading dye
  • Gel : 1%

Expected size :

  • NarK, NarG, NirB : 500 bp

We obtain fragments at the good size for all the colony. We will make a culture of DH5α with BBa_K1155004, BBa_K1155005 and BBa_K1155006. We will also sequence our plasmids.

2 - Liquid culture of DH5α with BBa_K1155004, BBa_K1155005 and BBa_K1155006

Xiaoing, Anaïs

Used quantities :

  • LB : 5mL
  • Chloramphénicol (1000X, 20µg/mL) : 5µL
  • BBa_K1155004, BBa_K1155005 and BBa_K1155006 : 25µL

We let the incubation over night at 37°C at 180 RPM.

We used colonies number 6, 7 and 8 for each promotor.

Objective : obtaining BBa_K1155007

1 - Electroelution of BBa_I732017 digested by EcoRI/SpeI

Nadia

Protocol : Electroelution

The electroelution was good. We will ligate RBS-LacZ with Term and PSB1C3.

Objective : obtaining biobricks in PSB3K3

1 - Extraction of BBa_J04450 from DH5α

Abdou

Protocol : Low copy plamid extraction

B - PCB sensing system

Objective : obtaining BBa_K1155002

1 - Sequence analysis for BBa_K1155002 in clones 4, 17 and 22

The sequence is good for each clone. We obtain a new biobrick : BBa_K1155002.


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