Team:Warsaw/Calendar-Main/30 June 2009
From 2009.igem.org
PCR inv
Kama
Tasks:
- Amplification of inv
Methods:
PCR mixture's composition:
2,5ul pfu buffer (Fermentas), 2,5ul MgSO4 (Fermentas), 1,5ul primers, 1ul dNTPs (10 mM)(new), 1ul template (Yersinia), 0,5ul pfu turbo polymerase (KNGiE), 1ul DMSO solution was topped up with H2O to 25ul.
- PCR programs:
inv
4min 95°C
(30s 95°C, 1min 54°C , 4min15s 72°C)x31
10min 72°C
~ 7°C
- Electrophoretic separation on 1% agarose gel
- Gel (from left)
- GeneRuler DNA Ladder Mix #SM0333 (Fermentas)
- inv
- inv control -
- No product
- Transformation of E. coli DH5alfa
iiiiii {{WarNotebookEnd}}
Results:
Notes:
cox sequence
Seba
Tasks:
Methods: