Paris/July 30

From 2007.igem.org

< Paris(Difference between revisions)
(→Ligations)
 
(5 intermediate revisions not shown)
Line 1: Line 1:
 +
[[Paris/July 29|yesterday]] -- [[Paris/July 31|tomorrow]] <br>
== Sequences ==
== Sequences ==
All the biobricks that we got from the plate and all the ligations that succeeded up to now.
All the biobricks that we got from the plate and all the ligations that succeeded up to now.
Line 239: Line 240:
|2µl
|2µl
|control of D35 digestion
|control of D35 digestion
-
|
+
|1
|- style="background: #cccccc;"   
|- style="background: #cccccc;"   
| style="background: #ccffcc;" |Control 3
| style="background: #ccffcc;" |Control 3
Line 247: Line 248:
|2µl
|2µl
|control of D34 digestion
|control of D34 digestion
-
|
+
|2
|- style="background: #cccccc;"   
|- style="background: #cccccc;"   
| style="background: #ccffcc;" |L3''
| style="background: #ccffcc;" |L3''
Line 263: Line 264:
|2
|2
|construction of the biobrick J23100-lox66dapAsubtilis
|construction of the biobrick J23100-lox66dapAsubtilis
-
|
+
|0
|- style="background: #cccccc;"   
|- style="background: #cccccc;"   
| style="background: #ccffcc;" |L7''
| style="background: #ccffcc;" |L7''
Line 271: Line 272:
|2
|2
|construction of the biobrick J23100- lox-ftsZ
|construction of the biobrick J23100- lox-ftsZ
-
|
+
|0
|- style="background: #cccccc;"   
|- style="background: #cccccc;"   
| style="background: #ccffcc;" |L8''
| style="background: #ccffcc;" |L8''
Line 279: Line 280:
|2
|2
|construction of the biobrick J23107- lox-ftsZ
|construction of the biobrick J23107- lox-ftsZ
-
|
+
|0
|- style="background: #cccccc;"   
|- style="background: #cccccc;"   
| style="background: #ccffcc;" |L9''
| style="background: #ccffcc;" |L9''
Line 295: Line 296:
|2
|2
|lox71 cloned as a biobrick in pSB1A2
|lox71 cloned as a biobrick in pSB1A2
-
|
+
|0
|- style="background: #cccccc;"   
|- style="background: #cccccc;"   
| style="background: #ccffcc;" |L11
| style="background: #ccffcc;" |L11
Line 303: Line 304:
|2
|2
|construction of the biobrick: J23107 promotor-lox66dapAsubtilis
|construction of the biobrick: J23107 promotor-lox66dapAsubtilis
-
|
+
|1
|- style="background: #cccccc;"   
|- style="background: #cccccc;"   
| style="background: #ccffcc;" |L12
| style="background: #ccffcc;" |L12
|D26.1 (gfp-tripart BI)
|D26.1 (gfp-tripart BI)
|4
|4
-
|D35 (lox66 plasmid digested as a BV)
+
|D35 (lox71 plasmid digested as a BV)
|2
|2
-
|construction of the biobrick lox66-gfp
+
|construction of the biobrick lox71-gfp
-
|
+
|14
|- style="background: #cccccc;"   
|- style="background: #cccccc;"   
| style="background: #ccffcc;" |L13
| style="background: #ccffcc;" |L13
|D13.2 (mRFP de pJ23100)
|D13.2 (mRFP de pJ23100)
|4
|4
-
|D34 (lox71 plasmid digested as a BV)
+
|D34 (lox66 plasmid digested as a BV)
|2
|2
-
|lox71 cloned as a biobrick
+
|construction of the biobrick lox66-mRFP
-
|
+
|0
|- style="background: #cccccc;"   
|- style="background: #cccccc;"   
| style="background: #ccffcc;" |L14
| style="background: #ccffcc;" |L14
Line 335: Line 336:
|2
|2
|J23107-RBS-Cre
|J23107-RBS-Cre
-
|
+
|0
|- style="background: #cccccc;"   
|- style="background: #cccccc;"   
| style="background: #ccffcc;" |L16
| style="background: #ccffcc;" |L16
Line 343: Line 344:
|2
|2
|J23100-lox71-ftsAftsZ
|J23100-lox71-ftsAftsZ
-
|
+
|0
|- style="background: #cccccc;"   
|- style="background: #cccccc;"   
| style="background: #ccffcc;" |L17
| style="background: #ccffcc;" |L17
Line 351: Line 352:
|2
|2
|J23107-lox71-ftsAftsZ
|J23107-lox71-ftsAftsZ
-
|
+
|0
|- style="background: #cccccc;"   
|- style="background: #cccccc;"   
| style="background: #ccffcc;" |L18
| style="background: #ccffcc;" |L18
Line 359: Line 360:
|2
|2
|J23100-RBSdapAsubtilis
|J23100-RBSdapAsubtilis
-
|
+
|0
|- style="background: #cccccc;"   
|- style="background: #cccccc;"   
| style="background: #ccffcc;" |L19
| style="background: #ccffcc;" |L19
Line 367: Line 368:
|2
|2
|J23107-RBSdapAsubtilis
|J23107-RBSdapAsubtilis
-
|
+
|0
|- style="background: #cccccc;"   
|- style="background: #cccccc;"   
| style="background: #ccffcc;" |L20
| style="background: #ccffcc;" |L20
Line 375: Line 376:
|2
|2
|
|
-
|
+
|0
|- style="background: #cccccc;"   
|- style="background: #cccccc;"   
| style="background: #ccffcc;" |L21
| style="background: #ccffcc;" |L21
Line 383: Line 384:
|2
|2
|
|
-
|
+
|0
|- style="background: #cccccc;"   
|- style="background: #cccccc;"   
| style="background: #ccffcc;" |L22
| style="background: #ccffcc;" |L22
Line 391: Line 392:
|2
|2
|
|
-
|
+
|0
|- style="background: #cccccc;"   
|- style="background: #cccccc;"   
| style="background: #ccffcc;" |L23
| style="background: #ccffcc;" |L23
Line 399: Line 400:
|2  
|2  
|
|
-
|
+
|1
|- style="background: #cccccc;"   
|- style="background: #cccccc;"   
| style="background: #ccffcc;" |L24
| style="background: #ccffcc;" |L24
Line 407: Line 408:
|2
|2
|
|
-
|
+
|0
|- style="background: #cccccc;"   
|- style="background: #cccccc;"   
| style="background: #ccffcc;" |L25
| style="background: #ccffcc;" |L25
Line 415: Line 416:
|2  
|2  
|
|
-
|
+
|1
|}
|}
Line 431: Line 432:
* L1".1, L1".2  
* L1".1, L1".2  
* L6".1, L6".2
* L6".1, L6".2
 +
 +
 +
== Sequencing ==
 +
 +
The following sequencing reactions have been performed
 +
 +
DB_MP1.1+O18
 +
DB_MP1.1+O19
 +
DB_MP1.2+O18
 +
DB_MP1.2+O19
 +
DB_MP2.1+O18
 +
DB_MP2.1+O19
 +
DB_MP3.1+O18
 +
DB_MP3.1+O19
 +
DB_MP3.2+O18
 +
DB_MP3.2+O19
 +
DB_MP4.1+O18
 +
DB_MP4.1+O19
 +
DB_MP4.2+O18
 +
DB_MP4.2+O19
 +
DB_MP5.1+O18
 +
DB_MP5.1+O19
 +
DB_MP5.2+O18
 +
DB_MP5.2+O19
 +
DB_MP6.1+O18
 +
DB_MP6.1+O19
 +
DB_MP6.2+O18
 +
DB_MP6.2+O19
 +
DB_MP7.1+O18
 +
DB_MP7.1+O19
 +
DB_MP7.2+O18
 +
DB_MP7.2+O19
 +
DB_MP8.1+O18
 +
DB_MP8.1+O19
 +
DB_MP8.2+O18
 +
DB_MP8.2+O19
 +
DB_MP9.1+O18
 +
DB_MP9.1+O19
 +
DB_MP9.2+O18
 +
DB_MP9.2+O19
 +
DB_MP10.1+O18
 +
DB_MP10.1+O19
 +
DB_MP10.2+O18
 +
DB_MP10.2+O19
 +
DB_MP11.3+O18
 +
DB_MP11.3+O19
 +
DB_MP11.4+O18
 +
DB_MP11.4+O19
 +
DB_MP12.1+O18
 +
DB_MP12.1+O19
 +
DB_MP12.2+O18
 +
DB_MP12.2+O19
 +
DB_L1.2+O18
 +
DB_L1.2+O19
 +
DB_L1.3+O18
 +
DB_L1.3+O19
 +
DB_L2.1+O18
 +
DB_L2.1+O19
 +
DB_L2.2+O18
 +
DB_L2.2+O19
 +
DB_L9+O18
 +
DB_L9+O19
 +
DB_L10+O18
 +
DB_L10+O19
 +
DB_L6.1+O18
 +
DB_L6.1+O19
 +
DB_L6.2+O18
 +
DB_L6.2+O19
 +
DB_L6.3+O18
 +
DB_L6.3+O19

Latest revision as of 17:52, 7 October 2007

yesterday -- tomorrow

Contents

Sequences

All the biobricks that we got from the plate and all the ligations that succeeded up to now.


Colonies PCR screen

On colony PCRs performed to screen for correct ligation reactions (performed on 27/07/07):

10 clones of L1 ligation reactions, 6 clones of L6 ligation reactions

preparation of the following PCR mix

  • 18x (12.5µL 2xreaction mix)= 225
  • 18x (0.5µL oligo O18 VF2 10µM)=9
  • 18x (0.5µL oligo O19 VR 10µM)=9
  • 12µL H20+colony (10min 100°)

PCRs

PCR : P5 lox66-DapAColi
PCR Settings Buffer (5x) 5x 10µL Expected size
Annealing (°C) MgCl2 10µM 10µM 0µL 985
55 dNTP 10µM 10µM 1µL Success
Time Elongation Oligo F 10µM O6 2.5µL
2m00' Oligo R 10µM O7 2.5µL Image (click to enlarge)
Number cycles Water 34µl [[Image:|30px]]
30 Polymerase Phusion 0.5µL Band (0=ladder)
DNA Toothpick in MG16655 Glycerol


PCR : P6 Lox66-DapASubtilis
PCR Settings Buffer (5x) 5x 10µL Expected size
Annealing (°C) MgCl2 10µM 10µM 0µL 979
55 dNTP 10µM 10µM 1µL Success
Time Elongation Oligo F 10µM O8 2.5µL
2m00' Oligo R 10µM O9 2.5µL Image (click to enlarge)
Number cycles Water 34µl [[Image:|30px]]
30 Polymerase Phusion 0.5µL Band (0=ladder)
DNA 0.5µl Subtilis DNA


PCR : P7 Lox71-FtsZ
PCR Settings Buffer (5x) 5x 10µL Expected size
Annealing (°C) MgCl2 10µM 10µM 0µL 1260
55 dNTP 10µM 10µM 1µL Success
Time Elongation Oligo F 10µM O1 2.5µL
2m00' Oligo R 10µM O2 2.5µL Image (click to enlarge)
Number cycles Water 34µl [[Image:|30px]]
30 Polymerase Phusion 0.5µL Band (0=ladder)
DNA Toothpick in MG16655 Glycerol


PCR : P8 RBS-DapAColi
PCR Settings Buffer (5x) 5x 10µL Expected size
Annealing (°C) MgCl2 10µM 10µM 0µL 952
55 dNTP 10µM 10µM 1µL Success
Time Elongation Oligo F 10µM O20 2.5µL
2m00' Oligo R 10µM O7 2.5µL Image (click to enlarge)
Number cycles Water 34µl [[Image:|30px]]
30 Polymerase Phusion 0.5µL Band (0=ladder)
DNA Toothpick in MG16655 Glycerol


PCR : P11 Lox71-KmR-Lox66
PCR Settings Buffer (5x) 5x 10µL Expected size
Annealing (°C) MgCl2 10µM 10µM 0µL 1084
55 dNTP 10µM 10µM 1µL Success
Time Elongation Oligo F 10µM O10 2.5µL
2m00' Oligo R 10µM O11 2.5µL Image (click to enlarge)
Number cycles Water 34µl [[Image:|30px]]
30 Polymerase Phusion 0.5µL Band (0=ladder)
DNA 0.5 µl MP12

Digestion reactions

The following digestion reactions have been performed:

Digestion Products
Number Product Name Matrix Name Enzyme 1 Enzyme 2 size Description
D19' BB dig. lox66DapAsubtilis lox66-DapAsubtilis P6' PCR product EcoRI PstI ~960 PCR product digested for cloning as a BioBrick
D21' bw-insert lox66-DapAsubtilis lox66-DapAsubtilis P6' PCR product XbaI PstI ~960 PCR product digested for cloning as a BI
D27' lox71-ftsZ bw-insert lox71-ftsZ PCR product P7 XbaI PstI lox71-ftsZ(unmutated) ready for use as a backward insert
D33 RBS(B0030)CreORF L6' (clone 1 & 2) XbaI PstI RBS-Cre digestion for use as a BI
D34 lox66 L9' lox66 SpeI PstI Biobrick plasmid carrying lox66 digested as a BV
D35 lox71 L10' lox71 SpeI PstI Biobrick plasmid carrying lox71 digested as a BV

Ligations

Ligations
Number Insert Insert Volume (µL) Vector Vector Volume (µL) Comments Number of colonies
Control 1 MP3.1 digested with EcoRI (D0) 2 control of ligation efficiency
a faire MP3.1 digested with EcoRI (D0) 2 without ligase in the mix: control of digestion efficiency
Control 2 D35 2µl control of D35 digestion 1
Control 3 D34 2µl control of D34 digestion 2
L3 D19 (lox66dapAsubtilis) 4 D22.1 (pSB1A2 dig. EcoRI&PstI) 2 Insertion of lox66DapASubtilis as a biobrick
L5 D21’(lox66DapASubtilis) 4 D1 (j23100 digested for CDS insertion) 2 construction of the biobrick J23100-lox66dapAsubtilis 0
L7 D27' (lox-ftsZ) 4 D1 (j23100 digested for CDS insertion) 2 construction of the biobrick J23100- lox-ftsZ 0
L8 D27' (lox-ftsZ) 4 D3 (j23107 digested for CDS insertion) 2 construction of the biobrick J23107- lox-ftsZ 0
L9 lox66 [O14+O15] (2µM) 2 D22.2 (pSB1A2 Eco, Pst) 2 lox66 cloned as a biobrick in pSB1A2
L10 lox71 [O16+O17] (2µM) 2 D22.2 (pSB1A2 dig. EcoRI & PstI) 2 lox71 cloned as a biobrick in pSB1A2 0
L11 D21’(lox66dapAsubtilis BI) 4 D3 (j23107 digested for CDS insertion) 2 construction of the biobrick: J23107 promotor-lox66dapAsubtilis 1
L12 D26.1 (gfp-tripart BI) 4 D35 (lox71 plasmid digested as a BV) 2 construction of the biobrick lox71-gfp 14
L13 D13.2 (mRFP de pJ23100) 4 D34 (lox66 plasmid digested as a BV) 2 construction of the biobrick lox66-mRFP 0
L14 D33.1 (RBS-Cre BI) 4 D1 (j23100 digested for CDS insertion) 2 J23100-RBS-Cre
L15 D33.1 (RBS-Cre BI) 4 D3 (j23107 digested for CDS insertion) 2 J23107-RBS-Cre 0
L16 D32 (lox71-ftsAftsZ BI) 4 D1 (j23100 digested for CDS insertion) 2 J23100-lox71-ftsAftsZ 0
L17 D32 (lox71-ftsAftsZ BI) 4 D3 (j23107 digested for CDS insertion) 2 J23107-lox71-ftsAftsZ 0
L18 D31 (RBSdapAsubtilis BI) 4 D1 (j23100 digested for CDS insertion) 2 J23100-RBSdapAsubtilis 0
L19 D31 (RBSdapAsubtilis BI) 4 D3 (j23107 digested for CDS insertion) 2 J23107-RBSdapAsubtilis 0
L20 D30 (RBSdapAsubtilis dig. BB) 4 D22.2 (pSB1A2 Eco, Pst) 2 0
L21 D29 4 D1 (j23100 digested for CDS insertion) 2 0
L22 D29 4 D3 (j23107 digested for CDS insertion) 2 0
L23 D28 (RBSdapAcoli dig.BB) 4 D22.2 (pSB1A2 Eco, Pst) 2 1
L24 D21’(lox66dapAsubtilis BI) 4 D3 (j23107 digested for CDS insertion) 2 0
L25 D36 (lox71-KmR-lox66 dig. BB) 4 D22.2 (pSB1A2 dig. EcoRI & PstI) 2 1

Ligation mix:

  • 1µl 10x buffer
  • 0.5µl Ligase
  • 2µL plasmid DNA solution
  • 4µL insert DNA solution

Reaction in 10µl

ON @ 4°C

MiniPreps

  • L1".1, L1".2
  • L6".1, L6".2


Sequencing

The following sequencing reactions have been performed

DB_MP1.1+O18 DB_MP1.1+O19 DB_MP1.2+O18 DB_MP1.2+O19 DB_MP2.1+O18 DB_MP2.1+O19 DB_MP3.1+O18 DB_MP3.1+O19 DB_MP3.2+O18 DB_MP3.2+O19 DB_MP4.1+O18 DB_MP4.1+O19 DB_MP4.2+O18 DB_MP4.2+O19 DB_MP5.1+O18 DB_MP5.1+O19 DB_MP5.2+O18 DB_MP5.2+O19 DB_MP6.1+O18 DB_MP6.1+O19 DB_MP6.2+O18 DB_MP6.2+O19 DB_MP7.1+O18 DB_MP7.1+O19 DB_MP7.2+O18 DB_MP7.2+O19 DB_MP8.1+O18 DB_MP8.1+O19 DB_MP8.2+O18 DB_MP8.2+O19 DB_MP9.1+O18 DB_MP9.1+O19 DB_MP9.2+O18 DB_MP9.2+O19 DB_MP10.1+O18 DB_MP10.1+O19 DB_MP10.2+O18 DB_MP10.2+O19 DB_MP11.3+O18 DB_MP11.3+O19 DB_MP11.4+O18 DB_MP11.4+O19 DB_MP12.1+O18 DB_MP12.1+O19 DB_MP12.2+O18 DB_MP12.2+O19 DB_L1.2+O18 DB_L1.2+O19 DB_L1.3+O18 DB_L1.3+O19 DB_L2.1+O18 DB_L2.1+O19 DB_L2.2+O18 DB_L2.2+O19 DB_L9+O18 DB_L9+O19 DB_L10+O18 DB_L10+O19 DB_L6.1+O18 DB_L6.1+O19 DB_L6.2+O18 DB_L6.2+O19 DB_L6.3+O18 DB_L6.3+O19

Retrieved from "http://2007.igem.org/wiki/index.php/Paris/July_30"