Team:DTU-Denmark/Notebook/30 July 2013
From 2013.igem.org
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
Conclusion
No right bands where acquired from PCR-amplification with genomic DNA template.
Navigate to the Previous or the Next Entry