Team:Paris Saclay/Notebook/July/8

From 2013.igem.org

(Difference between revisions)
(→2 - Electrophoresis of the digestion of BBa_K592009, BBa_I732017 by NotI, XhoI, EcoRI, EcoRI/PstI)
 
(10 intermediate revisions not shown)
Line 1: Line 1:
{{Team:Paris_Saclay/incl_debut_generique}}
{{Team:Paris_Saclay/incl_debut_generique}}
 +
='''Notebook : July 8'''=
='''Notebook : July 8'''=
-
 
-
 
-
 
-
==''Summary:''==
 
-
FNR regulator system:
 
-
*performed another digestion for AmilCP, Pfnr plus sequence LacZ with Not I, Xho I, EcoR I and PST I.
 
-
*electrophoresis for those digest products
 
-
*enrichment culture for clone of the briobrick BBa_K1155000
 
-
*electrophoresis for extracted products of last friday
 
-
 
-
=='''Lab work'''==
 
-
 
-
 
-
 
-
 
-
 
-
 
-
 
-
 
-
Overnight incubation at 37°C with agitation.
 
-
<br>
 
-
The electrophoresis for the plasmids which we had extracted last week plus 3 other BioBrick promoter Bph R1, promoter Bph A1, Bph R2.
 
-
 
-
Volume added:
 
-
*Pfnr2: 10µl
 
-
*R1P: 10µl
 
-
*R2: 10µl
 
-
*A1P: 10µl
 
-
 
-
 
-
Migration at 100V for 25mins then continued till 45 minutes:
 
-
<br>
 
-
Results:
 
-
 
-
{| align="center"
 
-
| style="width:350px;border:1px solid black;" | [[File:PS08071345.jpg|right|350px]]
 
-
| style="width:350px;border:1px solid black;" |
 
-
*Well 1 : R2
 
-
*Well 2 : R1P
 
-
*Well 3 : A1P
 
-
*Well 4 : Pfnr
 
-
*gel 0.8%
 
-
|}<br>
 
-
 
-
 
-
The concentration of Pfnr2 was detected by NanoDrop :
 
-
 
-
*C = 1788.8 ng/µl
 
-
*260/280 = 2.08
 
-
 
-
We considered that our extraction of plasmid DNA was not successful, we need to perform another extraction DNA.
 
-
 
-
 
-
 
-
 
-
 
-
 
-
 
-
 
-
 
-
 
-
 
-
 
-
 
-
 
-
 
-
<u>Electrophoresis band size estimation</u><br>
 
-
<p>We used Clonemanager for band size estimation:</p>
 
-
<br>
 
-
{| border="1" align="center"
 
-
|-
 
-
|Molecule
 
-
|enzymes(Buffer)
 
-
|Size
 
-
|-
 
-
|BBa_K1155000
 
-
|XHOI(Red)
 
-
|1289+892bp
 
-
|-
 
-
|BBa_K1155000
 
-
|ECoR I(Orange)
 
-
|2151bp
 
-
|}<br>
 
-
 
-
 
-
 
-
 
-
 
-
 
-
 
-
 
-
 
-
 
-
 
-
 
-
 
-
 
-
 
-
 
-
 
-
{{Team:Paris_Saclay/incl_debut_generique}}
 
-
 
-
='''Notebook : August 23'''=
 
=='''Lab work'''==
=='''Lab work'''==
Line 109: Line 7:
==='''A - Aerobic/Anaerobic regulation system'''===
==='''A - Aerobic/Anaerobic regulation system'''===
-
===='''Objective : Bba_K1155003, Bba_K1155007'''====
+
===='''Objective : BBa_K1155003, BBa_K1155007'''====
-
===='''1 - Digestion of Bba_K592009, Bba_K1155007 by NotI, XhoI, EcoRI, EcoRI/PstI'''====
+
===='''1 - Digestion of BBa_K592009, BBa_I732017 by NotI, XhoI, EcoRI, EcoRI/PstI'''====
Abou, Anaïs, Sheng, Zhou
Abou, Anaïs, Sheng, Zhou
Line 118: Line 16:
* NotI :  
* NotI :  
-
** Bba_K592009 : 2µL
+
** BBa_K592009 : 2µL
** Buffer orange : 2µL
** Buffer orange : 2µL
** NotI : 0.5µL
** NotI : 0.5µL
Line 124: Line 22:
* XhoI :  
* XhoI :  
-
** Bba_K592009 : 2µL
+
** BBa_K592009 : 2µL
** Buffer red : 2µL
** Buffer red : 2µL
** XhoI : 0.5µL
** XhoI : 0.5µL
Line 130: Line 28:
* EcoRI :  
* EcoRI :  
-
** Bba_K592009 : 2µL
+
** BBa_K592009 : 2µL
** Buffer orange : 2µL
** Buffer orange : 2µL
** EcoRI : 0.5µL
** EcoRI : 0.5µL
Line 136: Line 34:
* EcoRI/PstI :  
* EcoRI/PstI :  
-
** Bba_I732017 : 2µL
+
** BBa_I732017 : 2µL
** Buffer orange : 2µL
** Buffer orange : 2µL
** EcoRI : 0.5µL
** EcoRI : 0.5µL
Line 144: Line 42:
We let our digestion 1h30 at 37°C.
We let our digestion 1h30 at 37°C.
-
===='''2 - Electrophoresis of the digestion of Bba_K592009, Bba_I732017 by NotI, XhoI, EcoRI, EcoRI/PstI'''====
+
===='''2 - Electrophoresis of the digestion of BBa_K592009, BBa_I732017 by NotI, XhoI, EcoRI, EcoRI/PstI'''====
Abdou, Anaïs, Sheng, Zhou
Abdou, Anaïs, Sheng, Zhou
{|
{|
-
| style="width:350px;border:1px solid black;" |[[]]
+
| style="width:350px;border:1px solid black;" |[[File:Psgel0807.jpg|500px]]
| 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 : 5µL Bba_K592009 clone 1 digested by EcoRI+1µl of 6X loading dye
+
* Well 2 : 5µL BBa_K592009 clone 1 digested by EcoRI+1µL of 6X loading dye
-
* Well 3 : 5µL Bba_K592009 clone 2 digested by EcoRI+1µl of 6X loading dye
+
* Well 3 : 5µL BBa_K592009 clone 2 digested by EcoRI+1µL of 6X loading dye
-
* Well 4 : 5µL Bba_K592009 clone 1 digested by NotI+1µl of 6X loading dye
+
* Well 4 : 5µL BBa_K592009 clone 1 digested by NotI+1µL of 6X loading dye
-
* Well 5 : 5µL Bba_K592009 clone 2 digested by NotI+1µl of 6X loading dye
+
* Well 5 : 5µL BBa_K592009 clone 2 digested by NotI+1µL of 6X loading dye
-
* Well 6 : 5µL Bba_K592009 clone 1 digested by XhoI+1µl of 6X loading dye
+
* Well 6 : 5µL BBa_K592009 clone 1 digested by XhoI+1µL of 6X loading dye
-
* Well 7 : 5µL Bba_K592009 clone 2 digested by XhoI+1µl of 6X loading dye
+
* Well 7 : 5µL BBa_K592009 clone 2 digested by XhoI+1µL of 6X loading dye
-
* Well 8 : 5µL Bba_I732017 clone 1 digested by EcoRI/PstI+1µl of 6X loading dye
+
* Well 8 : 5µL BBa_I732017 clone 1 digested by EcoRI/PstI+1µL of 6X loading dye
-
* Well 9 : 5µL Bba_I732017 clone 2 digested by EcoRI/PstI+1µl of 6X loading dye
+
* Well 9 : 5µL BBa_I732017 clone 2 digested by EcoRI/PstI+1µL of 6X loading dye
* Well 10 : -
* Well 10 : -
* Well 11 : -
* Well 11 : -
Line 167: Line 65:
Expected sizes :  
Expected sizes :  
-
* Bba_K592009 digested by NotI : 2046bp + 693bp
+
* BBa_K592009 digested by NotI : 2046bp + 693bp
-
* Bba_K592009 digested by XhoI : 1842bp + 892bp
+
* BBa_K592009 digested by XhoI : 1842bp + 892bp
 +
* BBa_I732017 : 3093bp
 +
 
 +
{|
 +
| style="border:1px solid black;padding:5px;background-color:#DEDEDE;" |
 +
We obtain fragments at the right size. Our extraction was good.
 +
|}
 +
 
{| border="1" align="center"
{| border="1" align="center"

Latest revision as of 23:55, 4 October 2013

Navigation Home Team Project Labwork Notebook Human practices

Contents

Notebook : July 8

Lab work

A - Aerobic/Anaerobic regulation system

Objective : BBa_K1155003, BBa_K1155007

1 - Digestion of BBa_K592009, BBa_I732017 by NotI, XhoI, EcoRI, EcoRI/PstI

Abou, Anaïs, Sheng, Zhou

Used quantities :

  • NotI :
    • BBa_K592009 : 2µL
    • Buffer orange : 2µL
    • NotI : 0.5µL
    • H2O : 15.5µL
  • XhoI :
    • BBa_K592009 : 2µL
    • Buffer red : 2µL
    • XhoI : 0.5µL
    • H2O : 15.5µL
  • EcoRI :
    • BBa_K592009 : 2µL
    • Buffer orange : 2µL
    • EcoRI : 0.5µL
    • H2O : 15.5µL
  • EcoRI/PstI :
    • BBa_I732017 : 2µL
    • Buffer orange : 2µL
    • EcoRI : 0.5µL
    • PstI : 0.5µL
    • H2O : 15µL

We let our digestion 1h30 at 37°C.

2 - Electrophoresis of the digestion of BBa_K592009, BBa_I732017 by NotI, XhoI, EcoRI, EcoRI/PstI

Abdou, Anaïs, Sheng, Zhou

Psgel0807.jpg
  • Well 1 : 6µL DNA Ladder
  • Well 2 : 5µL BBa_K592009 clone 1 digested by EcoRI+1µL of 6X loading dye
  • Well 3 : 5µL BBa_K592009 clone 2 digested by EcoRI+1µL of 6X loading dye
  • Well 4 : 5µL BBa_K592009 clone 1 digested by NotI+1µL of 6X loading dye
  • Well 5 : 5µL BBa_K592009 clone 2 digested by NotI+1µL of 6X loading dye
  • Well 6 : 5µL BBa_K592009 clone 1 digested by XhoI+1µL of 6X loading dye
  • Well 7 : 5µL BBa_K592009 clone 2 digested by XhoI+1µL of 6X loading dye
  • Well 8 : 5µL BBa_I732017 clone 1 digested by EcoRI/PstI+1µL of 6X loading dye
  • Well 9 : 5µL BBa_I732017 clone 2 digested by EcoRI/PstI+1µL of 6X loading dye
  • Well 10 : -
  • Well 11 : -
  • Well 12 : 6µL DNA Ladder
  • Gel : 1%

Expected sizes :

  • BBa_K592009 digested by NotI : 2046bp + 693bp
  • BBa_K592009 digested by XhoI : 1842bp + 892bp
  • BBa_I732017 : 3093bp

We obtain fragments at the right size. Our extraction was good.


Previous week Back to calendar Next day

Retrieved from "http://2013.igem.org/Team:Paris_Saclay/Notebook/July/8"