Team:DTU-Denmark/Notebook/30 July 2013

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30 July 2013

Contents

lab 208


Main purpose


Make PCR on Nir with genomic DNA template. Amplify the pZE21 backbone with USER-primers for construction of the arabinose inducible system. Put His-tag on the cycAX construct.

Who was in the lab


Gosia, Kristian, Henrike, Julia

Procedure


PCR

  • pZE21::GFP SF and pZE21::RFP in duplicates with primers pair 13 on 55C and extension time 3:00.
  • cycAX in triplicates with primer pair 33 2 samples on 62C and 3:30 extension and 1 sample on 55C and extension 3:00.
  • None negative was made for each containing same things as real samples just MQ instead of template DNA.


Results


Gel on PCR from yesterday

  • 1kb ladder
  • Nir 1uL genomic template
  • Nir 3uL genomic template
  • Nir 7uL....
  • Nir 10uL....
  • Nir 12uL....
  • Nir 15uL....
  • Nir 1uL HindIII treated genomic template
  • Nir 3uL HindIII treated genomic template
  • Nir 7uL....
  • Nir 10uL....
  • Nir 12uL....
  • Nir 15uL....
  • Negative control
  • 1kb ladder

2013 07 30 gel nir genomic dna.jpg

Conclusion


No right bands where acquired from PCR-amplification with genomic DNA template.

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