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Team:Alberta/Notebook/Optimizations
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:Results: Diluting the dNTPs to a final concentration of 0.2mM yielded cleaner PCR products. | :Results: Diluting the dNTPs to a final concentration of 0.2mM yielded cleaner PCR products. | ||
*Aug 31, 2010: | *Aug 31, 2010: | ||
| - | :Experimented with the dNTP: | + | :Experimented with the dNTP:MgCl<sub>2</sub> ratios to see if it yielded cleaner and/or more PCR products while increasing the reaction volume to 50uL to increase the accuracy of measuring reagents. |
| - | :Results: Diluting | + | :Results: Diluting MgCl<sub>2</sub> to a final concentration of 2mM led to more specific PCR production without sacrificing too much of the quantity of desired products. |
*Sept 1, 2010: | *Sept 1, 2010: | ||
| - | :Tested different annealing temperatures ranging from 55 to 70 | + | :Tested different annealing temperatures ranging from 55<sup>o</sup>C to 70<sup>o</sup>C. |
| - | :Results: We did not find significant variation between the different annealing temperatures. We decided to go with 62 | + | :Results: We did not find significant variation between the different annealing temperatures. We decided to go with 62<sup>o</sup>C since it yielded more products. |
*Sept 2, 2010: | *Sept 2, 2010: | ||
:Tested different cycles of 15, 20 and 25. | :Tested different cycles of 15, 20 and 25. | ||
Revision as of 21:06, 27 October 2010
Optimizations
Project Timeline: Click on an image to see more information
PCR Using Universal Primers
- Aug 27, 2010:
- Tested different amount of dNTPs added to 30uL PCR reactions.
- Results: Diluting the dNTPs to a final concentration of 0.2mM yielded cleaner PCR products.
- Aug 31, 2010:
- Experimented with the dNTP:MgCl2 ratios to see if it yielded cleaner and/or more PCR products while increasing the reaction volume to 50uL to increase the accuracy of measuring reagents.
- Results: Diluting MgCl2 to a final concentration of 2mM led to more specific PCR production without sacrificing too much of the quantity of desired products.
- Sept 1, 2010:
- Tested different annealing temperatures ranging from 55oC to 70oC.
- Results: We did not find significant variation between the different annealing temperatures. We decided to go with 62oC since it yielded more products.
- Sept 2, 2010:
- Tested different cycles of 15, 20 and 25.
- Results: 25 Cycles produced a large enough quantity of PCR products for the amount of time required to run the program compared to the other cycles.
- Sept 10, 2010:
- Tested how the modification of using 1ng of template to 10ng will affect PCR efficiency.
- Results: No significance difference was seen.
BsaI Digestions
- Sept 7, 2010:
- Tested different amounts of DNA samples – 0.5, 1, 1.5 and 2 ug – that can be digested by BsaI at 37oC and 50oC for one hour with and without BSA.
- Results: At 1.5 ug and up, the digestion is not cut to completion at 37oC. All samples are cut at 50oC without BSA.
- Sept 8, 2010:
- Tested how many ug of DNA could be digested in one hour with only one uL (10 units) of BsaI at 50oC. We used samples containing 2.5, 5 and 7.5ug of DNA.
- Results: At 5ug, the DNA is not completely cut, but majority of it is cut.
- Sept 10, 2010:
- Tested 2 to 4 hour digestion incubations at 37oC and 50oC with BsaI to see whether enzyme activity is maintained longer at 37oC.
- Results: BsaI enzymatic activity is maintained longer at 37oC while at 50oC BsaI enzymatic activity is lost in 2 hours.
- Sept 13, 2010:
- Test how long it will take to digest 5ug of DNA with 1uL BsaI at 50oC.
- Results: Loss of enzymatic activity in one hour.
- Test to see if 10ug of DNA will be digested overnight at 37oC (approximately 16 hours).
- Sept 14, 2010:
- Results: The DNA was not cut completely.
