Team:Amsterdam/extra/diary

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<div id="content-area">
<div id="sub-menu" class="content-block">
<div id="sub-menu" class="content-block">
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<h1>Diary</h1>
+
<h1>Lab Diary</h1>
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11/05/2012
+
__NOTOC__
-
Gel electrophoresis of the PCR reaction performed on 10/05/2012. Non-specific products obtained. Repeat PCR? Change annealing temperature?
+
<html>
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<div align='center'>
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<table>
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<tr>
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<td colspan='5' align='center'><b>Table of Contents</b></td>
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</tr>
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<tr>
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<td>
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<a href='https://2012.igem.org/Team:Amsterdam/extra/diary#12.2F07.2F2012'>12/07/2012</a>
 +
</td>
 +
<td>
 +
<a href='https://2012.igem.org/Team:Amsterdam/extra/diary#11.2F07.2F2012'>11/07/2012</a>
 +
</td>
 +
<td>
 +
<a href='https://2012.igem.org/Team:Amsterdam/extra/diary#10.2F07.2F2012'>10/07/2012</a>
 +
</td>
 +
<td>
 +
<a href='https://2012.igem.org/Team:Amsterdam/extra/diary#09.2F07.2F2012'>09/07/2012</a>
 +
</td>
 +
<td>
 +
<a href='https://2012.igem.org/Team:Amsterdam/extra/diary#06.2F07.2F2012'>06/07/2012</a>
 +
</td>
 +
</tr>
 +
<tr>
 +
<td>
 +
<a href='https://2012.igem.org/Team:Amsterdam/extra/diary#05.2F07.2F2012'>05/07/2012</a>
 +
</td>
 +
<td>
 +
<a href='https://2012.igem.org/Team:Amsterdam/extra/diary#04.2F07.2F2012'>04/07/2012</a>
 +
</td>
 +
<td>
 +
<a href='https://2012.igem.org/Team:Amsterdam/extra/diary#03.2F07.2F2012'>03/07/2012</a>
 +
</td>
 +
<td>
 +
<a href='https://2012.igem.org/Team:Amsterdam/extra/diary#05.2F06.2F2012'>05/06/2012</a>
 +
</td>
 +
<td>
 +
<a href='https://2012.igem.org/Team:Amsterdam/extra/diary#01.2F06.2F2012'>01/06/2012</a>
 +
</td>
 +
</tr>
 +
<tr>
 +
<td>
 +
<a href='https://2012.igem.org/Team:Amsterdam/extra/diary#31.2F05.2F2012'>31/05/2012</a>
 +
</td>
 +
<td>
 +
<a href='https://2012.igem.org/Team:Amsterdam/extra/diary#30.2F05.2F2012'>30/05/2012</a>
 +
</td>
 +
<td>
 +
<a href='https://2012.igem.org/Team:Amsterdam/extra/diary#29.2F05.2F2012'>29/05/2012</a>
 +
</td>
 +
<td>
 +
<a href='https://2012.igem.org/Team:Amsterdam/extra/diary#25.2F05.2F2012'>25/05/2012</a>
 +
</td>
 +
<td>
 +
<a href='https://2012.igem.org/Team:Amsterdam/extra/diary#24.2F05.2F2012'>24/05/2012</a>
 +
</td>
 +
</tr>
 +
<tr>
 +
<td>
 +
<a href='https://2012.igem.org/Team:Amsterdam/extra/diary#23.2F05.2F2012'>23/05/2012</a>
 +
</td>
 +
<td>
 +
<a href='https://2012.igem.org/Team:Amsterdam/extra/diary#16.2F05.2F2012'>16/05/2012</a>
 +
</td>
 +
<td>
 +
<a href='https://2012.igem.org/Team:Amsterdam/extra/diary#14.2F05.2F2012'>14/05/2012</a>
 +
</td>
 +
<td>
 +
<a href='https://2012.igem.org/Team:Amsterdam/extra/diary#11.2F05.2F2012'>11/05/2012</a>
 +
</td>
 +
<td>
 +
</td>
 +
</tr>
 +
</table>
 +
</div>
 +
</html>
 +
<h4>12/07/2012</h4>
 +
Transformation of the plasmid containing the M.ScaI methyltransferase (pIDTSMART-AMP).
-
Ladder
+
<h4>11/07/2012</h4>
-
pET28a+ (1 ng for PCR)
+
Mini-prep BBa_J63009+BBa_J04450 and pSB1AT3+BBa_J45320. Elution in 25µl.
-
pET28a+ (10 ng for PCR)
+
Restriction digestion of BBa_J63009+BBa_J04450 with DraI and RsaI/XbaI.
-
peGFP (1 ng for PCR)
+
Restriction digestion of pSB1AT3+BBa_J45320 with ScaI and xhoI.
-
peGFP (10 ng for PCR)
+
-
Second PCR for peGFP and pET28a+. annealing temperature = 53˚C
+
Something went wrong with the digestions.....
-
Same results obtained..... :(
+
-
14/05/2012
+
Transformation:
-
PCR of pET28a+ and peGFP -> annealing temperature 56˚C. non-specific DNA products obtained for the vector. Increase annealing temperature? Gel extract?
+
1)pSB3C5+ BBa_J04450 (2012 iGEM distribution kit plate 1 Well 3C)
 +
2)pSB4C5+ BBa_J04450 (2012 iGEM distribution kit plate 1 Well 3E)
-
Ladder
+
<h4>10/07/2012</h4>
-
Original pT28a+  
+
Set overnight cultures for BBa_J63009+BBa_J04450 and pSB1AT3+BBa_J45320 for mini-prep.
-
Transformed pET28a+ (200 pg DNA for PCR)
+
-
Transformed pET28a+ (1ng DNA for PCR)
+
-
Original peGFP
+
-
Transformed peGFP (200 pg DNA for PCR)
+
-
Transformed peGFP (1 ng DNA for PCR)
+
-
Gel extraction of pET28a+ from TAE gel + ethidium bromide. Elution in 25 µl miliQ water.
+
<h4>09/07/2012</h4>
-
PCR No. 2 -> pET28a+ and peGFP -> annealing temperature 60˚C.
+
Symposium with all the dutch iGEM teams at Wageningen University.
-
16/05/2012
+
No plates for pSB1C3 again.... Noooooooooo!
-
pET28a+ (gel extracted)
+
<h4>06/07/2012</h4>
-
peGFP (gel extracted)
+
Re-transform pSB1C3!
-
Ladder
+
-
pET28a+ (PCR No.2 -> 14/05/2012)
+
-
peGFP (PCR No.2 -> 14/05/2012)
+
-
Still non-specific products observed for the PCR. Possible inter-change during gel extraction; pET28a+ and peGFP got mixed up?
+
The overnight culture for BBa_J63009+BBa_J04450 and pSB1AT3+BBa_J45320 turned pink! What is going on?
-
23/05/2012
+
At the end of the day -> BBa_J63009+BBa_J04450 and pSB1AT3+BBa_J45320 both contain RFP......the colonies should be reddish..... Oops....already threw them away. Awwwww start again then!
-
Repeat what was done on 14/05 (PCR Temp 60˚C + gel extraction.
+
-
Two products obtained and concentration seems too low. Pfffffff.... Repeat again......And this is only a test, hope it will work better for the actual experiments
+
<h4>05/07/2012</h4>
-
:(
+
Isolated colonies obtained for BBa_J63009+BBa_J04450 and pSB1AT3+BBa_J45320.
 +
Set up overnight liquid LB culture for each plasmid for mini-prep.
-
24/05/2012
+
<h4>04/07/2012</h4>
-
PCR pET28a+ -> annealing temperature 62˚C.
+
Plates show growth. Antibiotics are working! Swarming of bacteria. Unusable!
-
Ladder
+
Streak new plates with a single colony to obtain isolated colonies. Incubate overnight at 37˚C.
-
pET28a+
+
 +
Nothing grew on the pSB1C3 plate.
-
25/05/2012
+
<h4>03/07/2012</h4>
-
Pooled all the PCR strips containing pET28a+ for DNA precipitation reaction.
+
Prepared ampicillin and chloramphenicol stock solutions (50 mg/ml).
-
29/05/2012
+
Made LB/ampicillin and LB/chloramphenicol plates.
-
Gel electrophoresis of precipitated DNA pET28a+ from 25/05/2012
+
 
 +
Transformation:
 +
*pSB1AT3+BBa_J45320 (2012 iGEM distribution kit plate 2 Well 5J)
 +
*BBa_J63009+BBa_J04450 (2012 iGEM distribution kit plate 1 Well 1A)
 +
*pSB1C3 (2012 iGEM distribution kit linearised plasmid)
 +
Incubate overnight at 37˚C.06/06/2012
 +
Mini-prep of the colony obtained from Gibson on 05/06. Elution in 25µl miliQ water.
 +
Digestion of extracted plasmid with NotI and BglII (double digest).
 +
 
 +
[[File:Amsterdam_lab_diary_1.jpg|300px|border]]
Ladder
Ladder
-
Gel extracted pET28a+
+
Mini-prep colony digested with NotI and BglII
-
peGFP from 23/05
+
-
The pET28a+ is ready for the one step isothermal gibson assembly reaction. peGFP should also be gel extracted.
+
<h4>05/06/2012</h4>
 +
One colony obtained. Checked for fluorescence with GFP. No fluorescence.
 +
Prepared overnight culture with colony for mini-prep.
 +
<h4>01/06/2012</h4>
 +
Diewertje removed the plates from the incubator and put them at 4˚C for the weekend. Thank you Diewertje!
-
30/05/2012
+
<h4>31/05/2012</h4>
 +
Prepared LB agar for LB plates + Kanamycin.
 +
Gibson assembly of peGFP and pET28a+ in equimolar amounts.
 +
Transformation of 5µl of Gibson reaction mix in DH5 alpha competent bacteria. Incubation overnight at 37˚C.
 +
 
 +
<h4>30/05/2012</h4>
Prepared TAE and TBE gels with ethidium bromide.
Prepared TAE and TBE gels with ethidium bromide.
Pooled all the PCR products for peGFP and gel extract the correct band. Elution in 25µl miliQ water.
Pooled all the PCR products for peGFP and gel extract the correct band. Elution in 25µl miliQ water.
-
 
+
[[File:Amsterdam_lab_diary_2.jpg|300px|border]]
Ladder
Ladder
Line 82: Line 167:
Everything is ready! :)
Everything is ready! :)
-
31/05/2012
+
<h4>29/05/2012</h4>
-
Prepared LB agar for LB plates + Kanamycin.
+
Gel electrophoresis of precipitated DNA pET28a+ from 25/05/2012
-
Gibson assembly of peGFP and pET28a+ in equimolar amounts.
+
-
Transformation of 5µl of Gibson reaction mix in DH5 alpha competent bacteria. Incubation overnight at 37˚C.
+
-
01/06/2012
+
[[File:Amsterdam_lab_diary_3.jpg|300px|border]]
-
Diewertje removed the plates from the incubator and put them at 4˚C for the weekend. Thank you Diewertje!
+
 +
Ladder
 +
Gel extracted pET28a+
 +
peGFP from 23/05
-
05/06/2012
+
The pET28a+ is ready for the one step isothermal gibson assembly reaction. peGFP should also be gel extracted.
-
One colony obtained. Checked for fluorescence with GFP. No fluorescence.
+
-
Prepared overnight culture with colony for mini-prep.
+
-
06/06/2012
+
<h4>25/05/2012</h4>
-
Mini-prep of the colony obtained from Gibson on 05/06. Elution in 25µl miliQ water.
+
Pooled all the PCR strips containing pET28a+ for DNA precipitation reaction.
-
Digestion of extracted plasmid with NotI and BglII (double digest).
+
 
 +
<h4>24/05/2012</h4>
 +
PCR pET28a+ -> annealing temperature 62˚C.
 +
 
 +
[[File:Amsterdam_lab_diary_4.jpg|300px|border]]
Ladder
Ladder
-
Mini-prep colony digested with NotI and BglII
+
pET28a+
-
03/07/2012
+
<h4>23/05/2012</h4>
-
Prepared ampicillin and chloramphenicol stock solutions (50 mg/ml).
+
Repeat what was done on 14/05 (PCR Temp 60˚C + gel extraction.
-
Made LB/ampicillin and LB/chloramphenicol plates.
+
-
Transformation:
+
-
1)pSB1AT3+BBa_J45320 (2012 iGEM distribution kit plate 2 Well 5J)
+
-
2)BBa_J63009+BBa_J04450 (2012 iGEM distribution kit plate 1 Well 1A)
+
-
3)pSB1C3 (2012 iGEM distribution kit linearised plasmid)
+
-
Incubate overnight at 37˚C.
+
-
04/07/2012
+
[[File:Amsterdam_lab_diary_5.jpg|300px|border]]
-
Plates show growth. Antibiotics are working! Swarming of bacteria. Unusable!
+
-
Streak new plates with a single colony to obtain isolated colonies. Incubate overnight at 37˚C.
+
-
Nothing grew on the pSB1C3 plate.
+
-
05/07/2012
+
Two products obtained and concentration seems too low. Pfffffff.... Repeat again......And this is only a test, hope it will work better for the actual experiments
-
Isolated colonies obtained for BBa_J63009+BBa_J04450 and pSB1AT3+BBa_J45320.
+
:(
-
Set up overnight liquid LB culture for each plasmid for mini-prep.
+
-
06/07/2012
+
<h4>16/05/2012</h4>
-
Re-transform pSB1C3!
+
-
The overnight culture for BBa_J63009+BBa_J04450 and pSB1AT3+BBa_J45320 turned pink! What is going on?
+
-
At the end of the day -> BBa_J63009+BBa_J04450 and pSB1AT3+BBa_J45320 both contain RFP......the colonies should be reddish..... Oops....already threw them away. Awwwww start again then!
+
-
09/07/2012
+
[[File:Amsterdam_lab_diary_6.jpg|300px|border]]
-
Symposium with all the dutch iGEM teams at Wageningen University.
+
-
No plates for pSB1C3 again.... Noooooooooo!
+
-
10/07/2012
+
pET28a+ (gel extracted)
-
Set overnight cultures for BBa_J63009+BBa_J04450 and pSB1AT3+BBa_J45320 for mini-prep.
+
peGFP (gel extracted)
 +
Ladder
 +
pET28a+ (PCR No.2 -> 14/05/2012)
 +
peGFP (PCR No.2 -> 14/05/2012)
-
11/07/2012
+
Still non-specific products observed for the PCR. Possible inter-change during gel extraction; pET28a+ and peGFP got mixed up?
-
Mini-prep BBa_J63009+BBa_J04450 and pSB1AT3+BBa_J45320. Elution in 25µl.
+
-
Restriction digestion of BBa_J63009+BBa_J04450 with DraI and RsaI/XbaI.
+
-
Restriction digestion of pSB1AT3+BBa_J45320 with ScaI and xhoI.
+
-
Something went wrong with the digestions.....
+
-
Transformation:
+
-
1)pSB3C5+ BBa_J04450 (2012 iGEM distribution kit plate 1 Well 3C)
+
-
2)pSB4C5+ BBa_J04450 (2012 iGEM distribution kit plate 1 Well 3E)
+
-
12/07/2012
+
<h4>14/05/2012</h4>
-
Transformation of the plasmid containing the M.ScaI methyltransferase (pIDTSMART-AMP).
+
PCR of pET28a+ and peGFP -> annealing temperature 56˚C. non-specific DNA products obtained for the vector. Increase annealing temperature? Gel extract?
 +
 
 +
[[File:Amsterdam_lab_diary_7.jpg|300px|border]]
 +
 
 +
Ladder
 +
Original pT28a+
 +
Transformed pET28a+ (200 pg DNA for PCR)
 +
Transformed pET28a+ (1ng DNA for PCR)
 +
Original peGFP
 +
Transformed peGFP (200 pg DNA for PCR)
 +
Transformed peGFP (1 ng DNA for PCR)
 +
 
 +
Gel extraction of pET28a+ from TAE gel + ethidium bromide. Elution in 25 µl miliQ water.
 +
PCR No. 2 -> pET28a+ and peGFP -> annealing temperature 60˚C.
 +
 
 +
<h4>11/05/2012</h4>
 +
Gel electrophoresis of the PCR reaction performed on 10/05/2012. Non-specific products obtained. Repeat PCR? Change annealing temperature?
 +
 
 +
[[File:Amsterdam_lab_diary_8.jpg|300px|border]]
 +
 
 +
Ladder
 +
pET28a+ (1 ng for PCR)
 +
pET28a+ (10 ng for PCR)
 +
peGFP (1 ng for PCR)
 +
peGFP (10 ng for PCR)
 +
 
 +
Second PCR for peGFP and pET28a+. annealing temperature = 53˚C
 +
Same results obtained..... :(
</div>
</div>
</div>
</div>
{{Team:Amsterdam/Foot}}
{{Team:Amsterdam/Foot}}

Latest revision as of 11:46, 26 September 2012

Lab Diary

12/07/2012

Transformation of the plasmid containing the M.ScaI methyltransferase (pIDTSMART-AMP).

11/07/2012

Mini-prep BBa_J63009+BBa_J04450 and pSB1AT3+BBa_J45320. Elution in 25µl. Restriction digestion of BBa_J63009+BBa_J04450 with DraI and RsaI/XbaI. Restriction digestion of pSB1AT3+BBa_J45320 with ScaI and xhoI.

Something went wrong with the digestions.....

Transformation: 1)pSB3C5+ BBa_J04450 (2012 iGEM distribution kit plate 1 Well 3C) 2)pSB4C5+ BBa_J04450 (2012 iGEM distribution kit plate 1 Well 3E)

10/07/2012

Set overnight cultures for BBa_J63009+BBa_J04450 and pSB1AT3+BBa_J45320 for mini-prep.

09/07/2012

Symposium with all the dutch iGEM teams at Wageningen University.

No plates for pSB1C3 again.... Noooooooooo!

06/07/2012

Re-transform pSB1C3!

The overnight culture for BBa_J63009+BBa_J04450 and pSB1AT3+BBa_J45320 turned pink! What is going on?

At the end of the day -> BBa_J63009+BBa_J04450 and pSB1AT3+BBa_J45320 both contain RFP......the colonies should be reddish..... Oops....already threw them away. Awwwww start again then!

05/07/2012

Isolated colonies obtained for BBa_J63009+BBa_J04450 and pSB1AT3+BBa_J45320.

Set up overnight liquid LB culture for each plasmid for mini-prep.

04/07/2012

Plates show growth. Antibiotics are working! Swarming of bacteria. Unusable!

Streak new plates with a single colony to obtain isolated colonies. Incubate overnight at 37˚C.

Nothing grew on the pSB1C3 plate.

03/07/2012

Prepared ampicillin and chloramphenicol stock solutions (50 mg/ml).

Made LB/ampicillin and LB/chloramphenicol plates.

Transformation:

  • pSB1AT3+BBa_J45320 (2012 iGEM distribution kit plate 2 Well 5J)
  • BBa_J63009+BBa_J04450 (2012 iGEM distribution kit plate 1 Well 1A)
  • pSB1C3 (2012 iGEM distribution kit linearised plasmid)

Incubate overnight at 37˚C.06/06/2012 Mini-prep of the colony obtained from Gibson on 05/06. Elution in 25µl miliQ water. Digestion of extracted plasmid with NotI and BglII (double digest).

Amsterdam lab diary 1.jpg

Ladder Mini-prep colony digested with NotI and BglII

05/06/2012

One colony obtained. Checked for fluorescence with GFP. No fluorescence. Prepared overnight culture with colony for mini-prep.

01/06/2012

Diewertje removed the plates from the incubator and put them at 4˚C for the weekend. Thank you Diewertje!

31/05/2012

Prepared LB agar for LB plates + Kanamycin. Gibson assembly of peGFP and pET28a+ in equimolar amounts. Transformation of 5µl of Gibson reaction mix in DH5 alpha competent bacteria. Incubation overnight at 37˚C.

30/05/2012

Prepared TAE and TBE gels with ethidium bromide. Pooled all the PCR products for peGFP and gel extract the correct band. Elution in 25µl miliQ water.

Amsterdam lab diary 2.jpg

Ladder peGFP after gel extraction

Prepared the master mix for the Gibson assembly. Aliquoted 15µl in eppendorfs. Everything is ready! :)

29/05/2012

Gel electrophoresis of precipitated DNA pET28a+ from 25/05/2012

Amsterdam lab diary 3.jpg

Ladder Gel extracted pET28a+ peGFP from 23/05

The pET28a+ is ready for the one step isothermal gibson assembly reaction. peGFP should also be gel extracted.

25/05/2012

Pooled all the PCR strips containing pET28a+ for DNA precipitation reaction.

24/05/2012

PCR pET28a+ -> annealing temperature 62˚C.

Amsterdam lab diary 4.jpg

Ladder pET28a+

23/05/2012

Repeat what was done on 14/05 (PCR Temp 60˚C + gel extraction.

Amsterdam lab diary 5.jpg

Two products obtained and concentration seems too low. Pfffffff.... Repeat again......And this is only a test, hope it will work better for the actual experiments

(

16/05/2012

Amsterdam lab diary 6.jpg

pET28a+ (gel extracted) peGFP (gel extracted) Ladder pET28a+ (PCR No.2 -> 14/05/2012) peGFP (PCR No.2 -> 14/05/2012)

Still non-specific products observed for the PCR. Possible inter-change during gel extraction; pET28a+ and peGFP got mixed up?

14/05/2012

PCR of pET28a+ and peGFP -> annealing temperature 56˚C. non-specific DNA products obtained for the vector. Increase annealing temperature? Gel extract?

Amsterdam lab diary 7.jpg

Ladder Original pT28a+ Transformed pET28a+ (200 pg DNA for PCR) Transformed pET28a+ (1ng DNA for PCR) Original peGFP Transformed peGFP (200 pg DNA for PCR) Transformed peGFP (1 ng DNA for PCR)

Gel extraction of pET28a+ from TAE gel + ethidium bromide. Elution in 25 µl miliQ water. PCR No. 2 -> pET28a+ and peGFP -> annealing temperature 60˚C.

11/05/2012

Gel electrophoresis of the PCR reaction performed on 10/05/2012. Non-specific products obtained. Repeat PCR? Change annealing temperature?

Amsterdam lab diary 8.jpg

Ladder pET28a+ (1 ng for PCR) pET28a+ (10 ng for PCR) peGFP (1 ng for PCR) peGFP (10 ng for PCR)

Second PCR for peGFP and pET28a+. annealing temperature = 53˚C Same results obtained..... :(

Retrieved from "http://2012.igem.org/Team:Amsterdam/extra/diary"