Glasgow/Wetlab/Week10

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After the PCR raction, these were each digested with DpnI for 1 hour at 37°C and PCR purified according to QIAGEN manual.  After this they were transformed (15ul DNA into half a tube of TOP10 cells, heat shock of 30 seconds at 42°C, plated on carb) and labelled alphabetically according to PCR tubes above.
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[[User:MaijaP|Maija]] set up overnights in LB carb of colonies thought to contain (*a→d*) which were plated 23/08/07, labelled 1→10.
=== Wednesday 5th September 2007 ===
=== Wednesday 5th September 2007 ===

Revision as of 14:52, 10 September 2007

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Contents

Week 10

Monday 3rd September 2007

  1. Christine's plates from 31/08/07 all grew except for 1B. Overnights were set up from 7 colonies on each of the plates on Sunday, labelled 1A1→1H7, 49 in total as there were none from plate 1B. Christine, Maia and Maija miniprpped them and digested them as follows:
    This table is incorrect, see 04/09/07.
    PCR tube Colony DNA is taken from Insert Enzyme Expected sizes Result
    1A D (*a→d*) EcoRI 3455bp, 18bp, 3654bp Negative
    1B D (*a→d*) PstI 274bp, 6553bp Negative
    1C S (*d→g*) EcoRI 7046bp, 18bp, 284bp Negative
    1D S (*d→g*) PstI 1155bp, 2511bp, 3682bp Negative
    1E S (*d→g*) PstI 1962bp, 1704bp, 3682bp Negative
    1F Q (*d→g*) EcoRI 7046bp, 18bp, 284bp Negative
    1G Q (*d→g*) PstI 1155bp, 2511bp, 3682bp Negative
    1H Q (*d→g*) PstI 1962bp, 1704bp, 3682bp Negative

    Tuesday 4th September 2007

    1. Christine realised that the site directed mutagenesis she had attempted on Thursday 30/08/07 was wrong. S and Q were meant to be tested for (*a→d*), and D was meant to be tested for (*d→g*) but S and Q were tested for (*d→g*), and D was tested for (*a→d*). This means the digests from 03/09/07 were also incorrect. However, all is not lost because the sequencing results for S and D came back today and they show that both S and D contain (*d→g*). This means that, theoretically, digests of mutations 1C, 1D and 1E from 03/09/07 should be positive, but this is not the case.
    2. Before the sequencing results for S and D arrived, Christine set up site directed mutagenesis to correct that which she did 30/08/07. Used KOD and KOD_SDM programme as 30/08/07.
      PCR tube Colony DNA is taken from Insert Primers used
      1A D (*e→g*) EcoRI *E for + EcoRI *E rev
      1B D (*e→g*) PstI *E for + PstI *E rev
      1C D (*e→g*) PstI *F for + PstI *F rev
      1D S (*a→d*) EcoRI *B for + EcoRI *B rev
      1E S (*a→d*) PstI *C for + PstI *C rev
      1F Q (*a→d*) EcoRI *B for + EcoRI *B rev
      1G Q (*a→d*) PstI *C for + PstI *C rev

      After the PCR raction, these were each digested with DpnI for 1 hour at 37°C and PCR purified according to QIAGEN manual. After this they were transformed (15ul DNA into half a tube of TOP10 cells, heat shock of 30 seconds at 42°C, plated on carb) and labelled alphabetically according to PCR tubes above.

    3. Maija set up overnights in LB carb of colonies thought to contain (*a→d*) which were plated 23/08/07, labelled 1→10.

      Wednesday 5th September 2007

      Thursday 6th September 2007

      Friday 7th September 2007

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