Team:Paris Saclay/Notebook/August/1

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(3 - Electrophoresis of the PCR products : RBS-BphR2 Part I)
 
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===='''Objective : obtaining FNR and BphR2 proteins'''====
===='''Objective : obtaining FNR and BphR2 proteins'''====
-
===='''1 - Gel purification of PCR products : BphR2 Part I, BphR2, Part II, FNR Part I, FNR Part II, RBS-FNR Part I, PSB1C3 '''====
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===='''1 - Gel purification of PCR products : BphR2 Part I, BphR2 Part II, FNR Part I, FNR Part II, RBS-FNR Part I in plasmid pSB1C3 '''====
Xavier
Xavier
-
Protocol : [[Team:Paris_Saclay/Protocols/Gel purification|Gel purification]]
+
Protocol : [http://www.mn-net.com/tabid/1452/default.aspx Gel purification ]
Nanodrop :  
Nanodrop :  
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{|
{|
| style="border:1px solid black;padding:5px;background-color:#DEDEDE;" |
| style="border:1px solid black;padding:5px;background-color:#DEDEDE;" |
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CONCLUSION !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!
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The PCR products were good. Now we will do the Gibson assembly.
|}
|}
===='''2 - Gibson assembly.'''====
===='''2 - Gibson assembly.'''====
-
Xiaojing
+
Abdou, Xiaojing
Used quantities :  
Used quantities :  
* BphR2 :  
* BphR2 :  
-
** PSB1C3 : 2µL
+
** Gibson PCR of pSB1C3 : 2µL
** BphR2 Part I : 1µL  
** BphR2 Part I : 1µL  
** BphR2 Part II : 1µL  
** BphR2 Part II : 1µL  
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* FNR :  
* FNR :  
-
** PSB1C3 : 2µL
+
** Gibson PCR of pSB1C3 : 2µL
** FNR Part I : 1µL
** FNR Part I : 1µL
** FNR Part II : 1µL
** FNR Part II : 1µL
-
** Gisbon mix : 15µL ???????????????
+
** Gisbon mix : 15µL  
** H2O : 1µL
** H2O : 1µL
* RBS-FNR :
* RBS-FNR :
-
** PSB1C3 : 2µL
+
** Gibson PCR of pSB1C3: 2µL
** RBS-FNR Part I : 1µL
** RBS-FNR Part I : 1µL
** FNR Part II : 1µL
** FNR Part II : 1µL
-
** Gibson mix : 15µL ????????????
+
** Gibson mix : 15µL  
** H2O : 1µL
** H2O : 1µL
-
We let these mix at 50°C during 1h.
+
We incubated these Gibson assembly mixes at 50°C during 1h inside PCR machine.
-
===='''3 - PCR of : RBS-BphR2 Part I'''====
+
===='''3 - PCR of RBS-BphR2 Part I'''====
Abdou  
Abdou  
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** Oligo 55R : 1µL
** Oligo 55R : 1µL
** Buffer phusion : 5µL
** Buffer phusion : 5µL
-
** DNA : 0.25µL
+
** DNA (''P. pseudoalcaligenes'' KF 707 genomic DNA) : 0.25µL
-
** dNTP : 1µL
+
** dNTP 10mM : 1µL
-
** Phusion : ... µL 5 ?????????
+
** Enzyme Phusion : 5µL
** H2O : 36.5µL
** H2O : 36.5µL
PCR Program :  
PCR Program :  
-
[[File:PsPCRRBSBphR23007.jpg|400px]]
+
[[File:PsPCRBSBphR23007.jpg|400px]]
-
===='''4 - Gel purification of PCR of : RBS-BphR2 Part I'''====
+
===='''3 - Electrophoresis of the PCR products : RBS-BphR2 Part I'''====
-
????????
+
Xavier, XiaoJing
 +
 
 +
{|
 +
| style="width:350px;border:1px solid black;" |[[File:Psgel10108.jpg]]
 +
| style="width:350px;border:1px solid black;vertical-align:top;" |
 +
* Well 1 : 6µL of DNA Ladder
 +
* Well 2 : 5µL of RBS-BphR2 Part I + 1µl of 6X loading dye
 +
* Gel : 0.8%
 +
|}
 +
 
 +
Expected sizes :
 +
* RBS-BphR2 Part I : 197pb
 +
 
 +
{|
 +
| style="border:1px solid black;padding:5px;background-color:#DEDEDE;" |
 +
We obtained our fragment at the right size. We will purify it.
 +
|}
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 +
 
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{| border="1" align="center"
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|[[Team:Paris Saclay/Notebook/July/31|<big>Previous day</big>]]
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|[[Team:Paris_Saclay/Notebook|<big>Back to calendar</big>]]
 +
 
 +
|[[Team:Paris Saclay/Notebook/August/2|<big>Next day</big>]]
 +
|}
{{Team:Paris_Saclay/incl_fin}}
{{Team:Paris_Saclay/incl_fin}}

Latest revision as of 17:08, 3 October 2013

Contents

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Notebook : August 1

Lab work

A - Aerobic/Anaerobic regulation system / B - PCB sensing system

Objective : obtaining FNR and BphR2 proteins

1 - Gel purification of PCR products : BphR2 Part I, BphR2 Part II, FNR Part I, FNR Part II, RBS-FNR Part I in plasmid pSB1C3

Xavier

Protocol : [http://www.mn-net.com/tabid/1452/default.aspx Gel purification ]

Nanodrop :

  • BphR2 Part I : 44 ng/µL
  • BphR2 Part II : 64 ng/µL
  • FNR Part I : 147 ng/µL
  • FNR Part II : 140 ng/µL
  • RBS-FNR Part I : 167 ng/µL
  • PSB1C3 : 159 ng/µL

The PCR products were good. Now we will do the Gibson assembly.

2 - Gibson assembly.

Abdou, Xiaojing

Used quantities :

  • BphR2 :
    • Gibson PCR of pSB1C3 : 2µL
    • BphR2 Part I : 1µL
    • BphR2 Part II : 1µL
    • Gibson mix : 15µL
    • H2O : 1µL
  • FNR :
    • Gibson PCR of pSB1C3 : 2µL
    • FNR Part I : 1µL
    • FNR Part II : 1µL
    • Gisbon mix : 15µL
    • H2O : 1µL
  • RBS-FNR :
    • Gibson PCR of pSB1C3: 2µL
    • RBS-FNR Part I : 1µL
    • FNR Part II : 1µL
    • Gibson mix : 15µL
    • H2O : 1µL

We incubated these Gibson assembly mixes at 50°C during 1h inside PCR machine.

3 - PCR of RBS-BphR2 Part I

Abdou

Used quantities :

    • Oligo 54F : 1µL
    • Oligo 55R : 1µL
    • Buffer phusion : 5µL
    • DNA (P. pseudoalcaligenes KF 707 genomic DNA) : 0.25µL
    • dNTP 10mM : 1µL
    • Enzyme Phusion : 5µL
    • H2O : 36.5µL

PCR Program :

PsPCRBSBphR23007.jpg

3 - Electrophoresis of the PCR products : RBS-BphR2 Part I

Xavier, XiaoJing

Psgel10108.jpg
  • Well 1 : 6µL of DNA Ladder
  • Well 2 : 5µL of RBS-BphR2 Part I + 1µl of 6X loading dye
  • Gel : 0.8%

Expected sizes :

  • RBS-BphR2 Part I : 197pb

We obtained our fragment at the right size. We will purify it.


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