Team:Cambridge/Lab book/Week 10

From 2012.igem.org

(Difference between revisions)
(Thursday (30/08/12))
(Thursday (30/08/12))
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*Cycle settings:
*Cycle settings:
-
:*Melting - 98 &degC; - 10 seconds
+
:*Melting - 98 °C - 10 seconds
-
:*Annealing - 60 &degC; - 30 seconds
+
:*Annealing - 60 °C - 30 seconds
-
:*Elongation - 72 &degC; - 110 seconds
+
:*Elongation - 72 °C - 110 seconds
*Fragments of correct size produced for all except lane 5 produced. In this lane, DNA appears to have accumulated in the well, indicating it may be genomic. In future, will use lower numbers of template cells to avoid getting so much genomic DNA.
*Fragments of correct size produced for all except lane 5 produced. In this lane, DNA appears to have accumulated in the well, indicating it may be genomic. In future, will use lower numbers of template cells to avoid getting so much genomic DNA.

Revision as of 16:58, 31 August 2012

Week: 3 4 5 6 7 8 9 10 11 12

Contents

Monday (27/08/12)

Tuesday (28/08/12)

Wednesday (29/08/12)

Thursday (30/08/12)

PCR of Mg2+ riboswitch from genomic DNA


Gel from amplification of the riboswitch DNA. Lanes 2 + 3: with 8 codon substitution. Lanes 4 + 5: without 8 codon substitution.
  • Cycle settings:
  • Melting - 98 °C - 10 seconds
  • Annealing - 60 °C - 30 seconds
  • Elongation - 72 °C - 110 seconds
  • Fragments of correct size produced for all except lane 5 produced. In this lane, DNA appears to have accumulated in the well, indicating it may be genomic. In future, will use lower numbers of template cells to avoid getting so much genomic DNA.
  • Products extracted and purified.

Friday (31/08/12)

Saturday (01/09/12)

Sunday (02/09/12)