Team:Cambridge/Lab book/Week 5

From 2012.igem.org

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[[File:massgel3.jpg|center|200px|thumb|Vector amplification gel. Lanes 2-4 Lux containing vector. Lanes 5-7 Fluorescent construct vector. No products from these gels were amplified.]]
[[File:massgel3.jpg|center|200px|thumb|Vector amplification gel. Lanes 2-4 Lux containing vector. Lanes 5-7 Fluorescent construct vector. No products from these gels were amplified.]]
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*PCR fragments for Mg2+ riboswitch, luxA/mOrange fusion and fluorescent construct from yesterday separated on gels. 90mins at 100V.
*PCR fragments for Mg2+ riboswitch, luxA/mOrange fusion and fluorescent construct from yesterday separated on gels. 90mins at 100V.

Revision as of 10:18, 1 August 2012

Week: 3 4 5 6 7

Contents

Monday

Tuesday

Wednesday

Thursday

Hardware implementation


Our device, reaching perfection!


Our device is close to being implemented. The filtered photoresistors are placed now in the right position, the motory circuit is also functioning, the main chassis of the device is constructed and painted. However, the mirrors which will be used to surround the cuvettes are still missing and so is the mechanical coupler designed by us and being constructed at the Instrument shop of the Engineering Department. The device is also powered by a 9V battery, without the need to be connected to the computer.

PCR of vectors, CFP, YFP, Promotor, Terminator and mOrange


  • Plasmid PJS 130 used as our backbone for isolating the magnesium riboswitch and constructing the fluorescent ratiometric plasmid.
  • Parts from registry amplified: E0020 (CFP), B0015 (Terminator), K143083 (Pveg) and E0030 (YFP).
  • mOrange from lab also used
  • Primers:
  • E0020
  • Forward: cacaattaaaggaggaattcaaa|ATGGTGAGCAAGGGC
  • Reverse: tcgttttatttgatgcctgg|TTATTACTTGTACAGCTCGTCCA
  • B0015
  • Forward: acgagctgtacaagtaataa|CCAGGCATCAAATAAAACGA
  • Reverse: aaaattattttgacaaaatt|TATAAACGCAGAAAGGCCC
  • K143083
  • Forward: tgggcctttctgcgtttata|AATTTTGTCAAAATAATTTTATTG
  • Reverse: tcctcgcccttgctcaccat|ctagta|TTCACCACCTTTCTCTAGTAACA
  • E0030
  • Forward: tgttactagagaaaggtggtgaa|tactag|ATGGTGAGCAAGGGCG
  • Reverse: gatgcctggctctagtatca|TTATTACTTGTACAGCTCGTCCA
  • mOrange
  • Forward: accaaaaaggaatagagt|ATGGTGAGCAAGGGCG
  • Reverse: caaacttcat|ACTTCCTCCTCCTCCACTTCCTCCTCCTCC|cttgtaagctcgtccatgc
  • pJS130 Mg2+
  • Forward: tagaggaggtacgagtcccg|ATGAAACCAGTAACGTTATACGA
  • Reverse: tacatcacaattacggaaca|CAAAATCGTCTCCCTCC
  • pJS130 Fluorescent
  • Forward: acgagctgtacaagtaataa|TGATACTAGAGCCAGGCATC
  • Reverse: tcctcgcccttgctcaccat|TTTGAATTCCTCCTTTAATT
  • PCR settings:
  • 95 °C - 6mins
  • 98 °C - 10secs
  • 58 °C - 45secs
  • 72 °C - 180secs
  • Repeat above 35x
  • 72 °C - 5mins
  • 25 °C - 1min

PCR of riboswitch DNA from bacillus genome and Lux genes from e.coli genome


  • Colony of strain pJS130 used as template for riboswitch, colony of previously transformed e.coli used as template for lux operon.
  • M2+ RS
  • Forward: cggagggagacgattttg|TGTTCCGTAATTGTGATGTAAG
  • Reverse: tataacgttactggtttcat|CGGGACTCGTACCTCC
  • Lux operon
  • Forward: gctgtacaag|GGAGGAGGAGGAAGTGGAGGAGGAGGAAGT|atgaagtttggaaatatttgtttttc
  • Reverse: cctcgcccttgctcaccat|ACTCTATTCCTTTTTGGTGATTC
  • PCR settings - as above (run in parallel).

Friday

Gel electrophoresis of PCR products


Top: Mg2+ riboswitch gel. Lanes 6+7 positive and negative controls respectively for entire run. Lanes 3-5 genomic riboswitch amplification -8 codons. Lanes 2+3 vector -8 codons. Bottom: Various. Lanes 3-5 mOrange amplification. Lanes 6-8 CFP amplification. mOrange amplification did not work.
Top: Small products for fluorescent construct. Lanes 1-3 Terminator (B0015). Lanes 4-5 Promotor pVEG + RBS. Bottom: Various. Lanes 2-4 YFP amplification. Lanes 5-7 Mg2+ vector +8 codons. Lane 8 Mg2+ vector -8 codons. Lane 8 amplification did not work.
Vector amplification gel. Lanes 2-4 Lux containing vector. Lanes 5-7 Fluorescent construct vector. No products from these gels were amplified.





  • PCR fragments for Mg2+ riboswitch, luxA/mOrange fusion and fluorescent construct from yesterday separated on gels. 90mins at 100V.
  • Mostly successful, but will need to repeat four runs: Three vectors (fluorescent, fusion (lux) and Mg2+ riboswitch (-8 codons) and mOrange gene.