Team:Paris Saclay/Notebook/July/3

From 2013.igem.org

(Difference between revisions)
(→1 - Colony PCR of BBa_K1155000 to check good insertion of Pndh* in pSB1C3)
 
(8 intermediate revisions not shown)
Line 7: Line 7:
==='''A - Aerobic/Anaerobic regulation system'''===
==='''A - Aerobic/Anaerobic regulation system'''===
-
===='''Objective : obtaining Bba_K1155000'''====
+
===='''Objective : obtaining BBa_K1155000'''====
-
===='''1 - Colony PCR of Bba_K1155000 to check the good insertion of Pfnr in PSB1C3'''====
+
===='''1 - Colony PCR of BBa_K1155000 to check good insertion of Pndh* in pSB1C3'''====
Abdou, Sheng, Zhou
Abdou, Sheng, Zhou
Line 15: Line 15:
{|
{|
| style="border:1px solid black;padding:5px;background-color:#DE;" |
| style="border:1px solid black;padding:5px;background-color:#DE;" |
-
Tranformation of 07/02/13 works. We will do a Colony PCR of colonies.
+
Tranformation of 07/02/13 works. We will do a PCR colony.
|}
|}
-
Colonies count for Bba_K1155000 :  
+
Colonies count for BBa_K1155000 :  
* Standard concentration :  
* Standard concentration :  
-
** Bba_K1155000 : 0
+
** BBa_K1155000 : 0 colony
* High concentration :  
* High concentration :  
-
** Bba_K1155000 : 2
+
** BBa_K1155000 : 2 colonies
[[File:Ps0307jour.jpg|300px]]
[[File:Ps0307jour.jpg|300px]]
Line 30: Line 30:
<center>[[File:PSprimer07.jpg|right|250px]]</center>
<center>[[File:PSprimer07.jpg|right|250px]]</center>
<br>
<br>
-
'''Primer and PCR :'''
+
'''[https://2013.igem.org/Team:Paris_Saclay/Primers Primers] and PCR :'''
<p>'''VF2, VR, Pfnr_up, Pfnr_down are four oligos that we used for plasmid amplification. We used tree combinaisons VF/VR, VF/Pfnr_Down, Pfnr_Up/VR.'''
<p>'''VF2, VR, Pfnr_up, Pfnr_down are four oligos that we used for plasmid amplification. We used tree combinaisons VF/VR, VF/Pfnr_Down, Pfnr_Up/VR.'''
-
'''If the promoter Pfnr insert PSB1C3 plasmid successfully, tree fragments with specific size will be amplified.''' </p>
+
'''If the promoter Pndh* insert pSB1C3 plasmid successfully, tree fragments with specific size will be amplified.''' </p>
 +
'''
 +
Protocol'''
-
We mix each colony with 20µL of H2O.
+
We resuspend each colony with 20µL of H2O.
Used quantities :  
Used quantities :  
Line 40: Line 42:
* Mix : (it was divided in tubes for 4 different colonies for each oligo combinaison with 23µL of mix in each tube)  
* Mix : (it was divided in tubes for 4 different colonies for each oligo combinaison with 23µL of mix in each tube)  
** VF or Pfnr_Up : 6µL
** VF or Pfnr_Up : 6µL
-
** VR or Pfnr_Down or VR : 6µL
+
** VR or Pfnr_Down : 6µL
-
** dNTP : 6µL
+
** dNTP 10mM : 6µL
** Buffer Dream Taq : 30µL  
** Buffer Dream Taq : 30µL  
** Dream Taq : 6µL
** Dream Taq : 6µL
Line 48: Line 50:
[[File:PSPCR0307.jpg|400px]]
[[File:PSPCR0307.jpg|400px]]
-
===='''2 - Culture of Bba_K1155000 '''====
+
===='''2 - Culture of BBa_K1155000 '''====
Sheng
Sheng
-
We made new cultures by streaking 2 colonies of 07/02/13 culture of Bba_K1155000. We also did liquid culture of each one.   
+
We made new cultures by streaking 2 colonies of 07/02/13 culture of BBa_K1155000. We also did liquid culture of each one.   
-
We let culture at 37°C.
+
We incubate culture at 37°C.
-
===='''Objective : obtaining Bba_K1155003, Bba_K1155007'''====
+
===='''Objective : obtaining BBa_K1155003, BBa_K1155007'''====
-
===='''1 - Culture of Bba_I732017, Bba_K592009 '''====
+
===='''1 - Culture of BBa_I732017, BBa_K592009 '''====
Sheng  
Sheng  
Line 66: Line 68:
|}
|}
-
We made new cultures by streaking 2 colonies of 07/02/13 culture of Bba_I732017, Bba_K592009. We also did liquid culture of each one.   
+
We made new cultures by streaking 2 colonies of 07/02/13 culture of BBa_I732017, BBa_K592009. We also did liquid culture of each one.   
-
We let culture at 37°C.
+
We incubate culture at 37°C.

Latest revision as of 00:51, 5 October 2013

Navigation Home Team Project Labwork Notebook Human practices

Contents

Notebook : July 3

Lab work

A - Aerobic/Anaerobic regulation system

Objective : obtaining BBa_K1155000

1 - Colony PCR of BBa_K1155000 to check good insertion of Pndh* in pSB1C3

Abdou, Sheng, Zhou

Tranformation of 07/02/13 works. We will do a PCR colony.

Colonies count for BBa_K1155000 :

  • Standard concentration :
    • BBa_K1155000 : 0 colony
  • High concentration :
    • BBa_K1155000 : 2 colonies

Ps0307jour.jpg


PSprimer07.jpg


Primers and PCR :

VF2, VR, Pfnr_up, Pfnr_down are four oligos that we used for plasmid amplification. We used tree combinaisons VF/VR, VF/Pfnr_Down, Pfnr_Up/VR. If the promoter Pndh* insert pSB1C3 plasmid successfully, tree fragments with specific size will be amplified.

Protocol

We resuspend each colony with 20µL of H2O.

Used quantities :

  • DNA : 2µL
  • Mix : (it was divided in tubes for 4 different colonies for each oligo combinaison with 23µL of mix in each tube)
    • VF or Pfnr_Up : 6µL
    • VR or Pfnr_Down : 6µL
    • dNTP 10mM : 6µL
    • Buffer Dream Taq : 30µL
    • Dream Taq : 6µL
    • H2O : 246µL

PSPCR0307.jpg

2 - Culture of BBa_K1155000

Sheng

We made new cultures by streaking 2 colonies of 07/02/13 culture of BBa_K1155000. We also did liquid culture of each one. We incubate culture at 37°C.

Objective : obtaining BBa_K1155003, BBa_K1155007

1 - Culture of BBa_I732017, BBa_K592009

Sheng

Tranformation of 07/02/13 works. We will do new cultures.

We made new cultures by streaking 2 colonies of 07/02/13 culture of BBa_I732017, BBa_K592009. We also did liquid culture of each one. We incubate culture at 37°C.


Previous day Back to calendar Next day

Retrieved from "http://2013.igem.org/Team:Paris_Saclay/Notebook/July/3"