Team:Cambridge/Lab book/Week 7

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'''[[Team:Cambridge/Protocols/Chemicallycompetentcells|Production of chemically competent e.coli]]'''
'''[[Team:Cambridge/Protocols/Chemicallycompetentcells|Production of chemically competent e.coli]]'''
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----
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'''[[Team:Cambridge/Protocols/Gibsonassembly|Gibson assembly of magnesium riboswitch and fluorescent construct]]'''
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*NAD+ added to '''isothermal buffer'''*5 mix
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*Gel slices from yesterday (of vector fragment B) purified.
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*DNA added as follows:
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:*Tube 1:
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Revision as of 14:57, 7 August 2012

Week: 3 4 5 6 7

Contents

Monday

PCR of Magnesium riboswitch vector fragment B and Magnesium promoter

Riboswitch and promoter gel. Lanes 2+3: Fragment B without 8 codon substitution, lanes 4+5: Fragment B with 8 codon substitution, lanes 6+7: magnesium sensitive promoter, lane 8: +ve control
  • Normal PCR settings used, annealing temperature 57 °C, elongation step 90s long.
  • Lane 5 accidentally loaded with a DNA ladder instead of loading dye.
  • Expected fragment sizes:
  • Lane 2-5: 3kbp
  • Lane 6-7: 300bp
  • After electrophoresis, found vector products had, for the most part, worked. Promoter elements were not amplified - no band of the expected size was observed.
  • Positive control also failed, although this has ceased to work for several days, potentially due to DNA degradation.

Tuesday

Production of electrocompetent e.coli

Production of chemically competent e.coli

Gibson assembly of magnesium riboswitch and fluorescent construct

  • NAD+ added to isothermal buffer*5 mix
  • Gel slices from yesterday (of vector fragment B) purified.
  • DNA added as follows:
  • Tube 1:

Wednesday

Thursday

Friday

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