Team:HokkaidoU Japan/Notebook/August10
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==Single Colony Isolation== | ==Single Colony Isolation== | ||
* Observed if any colonies were made | * Observed if any colonies were made | ||
- | ** Could not see [[Team:HokkaidoU_Japan/ | + | ** Could not see [[Team:HokkaidoU_Japan/Parts#BioBricks|3-1E]] |
* Number of other colonies on other plates was also very small | * Number of other colonies on other plates was also very small | ||
** Mistake in protocol is inferred | ** Mistake in protocol is inferred |
Revision as of 07:04, 27 October 2010
Single Colony Isolation
- Observed if any colonies were made
- Could not see 3-1E
- Number of other colonies on other plates was also very small
- Mistake in protocol is inferred
- Precipitation of cells maybe at fault
- All but 3-1E was moved to new plates
PCR Reaction System
Reaction system was prepared for 3 parts, 245 uL in total
Reagent | Amount |
---|---|
Autoclaved DW | 165 uL |
10x PCR buffer | 25 uL |
2 mM dNTPs | 25 uL |
25 mM MgSO4 | 15 uL |
EX-F primer | 5 uL |
PS-R primer | 5 uL |
KOD plus Neo | 5 uL |
Total | 245 uL |
- 49 uL of reaction solution was added to each of 4 tubes and after DNA template was added
- Length of each template is listed int the table below
Tube | Biobrick | Length |
---|---|---|
1 | 2-24G(sender) | 847 bp |
2 | 1-2M(RBS) | 61 bp |
3 | 1-23L(terminator) | 178 bp |
4 | 3-1E(heat sensor) | 984 bp |
- Template DNA length is calculated by adding prefix and suffix length
- Biobrick Length + Prefix length + Suffix Length
- Because Mini prep of 3-1E failed, it amplified by PCR
PCR program
Predenature | 94℃ 2 min |
Denature | 98℃ 10 sec |
Extension | 68℃ 30 sec |
Hold | 4℃ |
- 30 cycles
- KOD potency is 30 sec/kbp, so 30 sec for1cycle
Electrophoresis
- Added 1 uL of 6xSample Buffer to 5 uL of amplified DNA
- Used marker pUC1d19/Hinf1
- Added 20 uL of EtBr to 1/2 TBE
Lane | DNA | Length of DNA |
---|---|---|
1 | pUC1d19/Hinf1 | |
2 | 2-24G(sender) | 847 bp |
3 | 1-2M(RBS) | 61 bp |
4 | 1-23L(terminator) | 178 bp |
5 | 3-1E(heat sensor) | 984 bp |