Team:UNIPV-Pavia/Notebook/Week2Jul

From 2009.igem.org

(Difference between revisions)
(July, 10th)
(July, 10th)
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*We also picked a colony from F2620 to infect 1 ml of LB + Amp. We incubated this inoculum with the others.
*We also picked a colony from F2620 to infect 1 ml of LB + Amp. We incubated this inoculum with the others.
 +
 +
*Gel results: all the picked colonies showed the expected amplicon of a correctly ligated plasmid! We decided to prepare a glycerol stock for:
 +
**A11-1
 +
**A11-3
 +
**A11-6
 +
 +
*Next week, only A11-1 will be used, but the other colonies will be used in case of failure.
 +
 +
*We also prepared a glycerol stock for F2620 culture.
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Revision as of 16:12, 10 July 2009

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December 2008
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March 2009
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April 2009
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May 2009
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June 2009
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July 2009
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August 2009
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September 2009
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October 2009
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November 2009
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Week from July 6th, to July 12nd, 2009

Previous Week Next Week

July, 6th

  • Digestion for:
R0011(E-X) BOL1(E-S)
  • Gel run/cut and band purification.
  • The purified DNA gave a good result at Nanodrop, but we decided to perform the entire work on BOL1 again because we were not sure that we had extracted a pure band.
  • We stored R0011(E-X) DNA at -20°C.
  • We infected 5 ml of LB + Amp with 8 ul of BOL1 glycerol stock to grow two identical overnight cultures (37°C, 220 rpm).



Preparation of experiment with Tecan F200

  • We picked a colony of B0030 plate (stored at +4°C) and infected 5 ml of LB + Amp.
  • We also infected 5 ml of LB + Amp with 10 ul of A1 and J23100 glycerol stocks.
  • We incubated the inocula overnight at 37°C, 220 rpm.

Top

July, 7th

  • Miniprep for BOL1 (X2).
  • Digestion for BOL1(E-S)(X2).
  • Gel run/cut/purification: none of the two BOL1 samples gave a good results in DNA quantification...we decided to cut the miniprepped plasmids again, but this time through an overnight digestion (both plasmids E-S).
  • In case of failure, we also infected 5 ml of LB + Amp with 8 ul of BOL1 glycerol stock to grow an overnight culture at 37°C, 220 rpm.
  • We prepared 0.5 l of LB + Amp.
  • We received sequencing results for:
    • T9002 - long part, but SEQUENCE CONFIRMED! while MIT results were "INCONSISTENT".
    • A10 - results showed a good chromatogram, but K117000 had not been correctly ligated. We will repeat this ligation one of the next weeks.


Preparation of experiment with Tecan F200

  • We diluted 1:100 the overnight cultures of A1, B0030 and J23100.
  • We incubated the diluted cultures for 5 hours (37°C, 220 rpm).



Experiment with Tecan F200

  • Description
  • Purpose:
  • Materials & Methods
  • Protocol
  • Results



Preparation of tomorrow's experiment with Tecan F200

  • We picked a colony from B0030 native plate (stored ad +4°C) and infected 5 ml of LB + Amp. We incubated the inoculum at 37°C, 220 rpm overnight.


Top

July, 8th

  • Gel run/cut/band purification for BOL1(E-S) overnight digestion. Results: gel showed that the enzymes had cut very well and this time also the purification gave a good quantification at Nanodrop.
  • We took R0011(E-X) stored ad -20°C and we were ready to ligate;)
  • Ligation:
    • A11: BOL1(E-S) + R0011(E-X) in pSB1A2
  • We incubated the ligation overnight at 16°C.



Preparation of experiment with Tecan F200

  • We diluted 1:100 the overnight culture of B0030.



Experiment with Tecan F200 (continues the next day)

  • Description
  • Purpose:
  • Materials & Methods
  • Protocol
  • Results

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July, 9th

  • We resuspended F2620 BioBrick from iGEM 2009 plates.
  • We transformed about 40 pg of the overnight ligation and 1 ul of the resuspended F2620 BioBrick. We plated transformed bacteria and incubated the two plates overnight at 37°C.



End of experiment with Tecan F200 (last measurement)

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July, 10th

  • A11 and F2620 overnight plates showed colonies!
  • Colony PCR for 6 colonies of A11 plate: the picked colonies were inoculated in 1 ml of LB + Amp and incubated at 37°C, 220 rpm waiting for PCR results.
  • We also picked a colony from F2620 to infect 1 ml of LB + Amp. We incubated this inoculum with the others.
  • Gel results: all the picked colonies showed the expected amplicon of a correctly ligated plasmid! We decided to prepare a glycerol stock for:
    • A11-1
    • A11-3
    • A11-6
  • Next week, only A11-1 will be used, but the other colonies will be used in case of failure.
  • We also prepared a glycerol stock for F2620 culture.

Top



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