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12/09/13
From 2013.igem.org
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(→Digestion of the samples purified with the enzyme PstI-HF and XbaI) |
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===Master Mix of the PstI/XbaI double digestion=== | ===Master Mix of the PstI/XbaI double digestion=== | ||
| + | *30 ul of cut samart buffer | ||
| + | *5 ul of PstI | ||
| + | *5 ul of XbaI | ||
| + | *58 ul of dH2O | ||
| + | **9.8 ul of the master mix were added to each reaction. | ||
| + | **2 ug DNA of each sample were digested. | ||
| + | '''Protocol''' | ||
| + | |||
| + | {|border=0.5 | ||
| + | |Sample||DNA volume||dH2O added to the final volume of 30ul | ||
| + | TODXF1||16.5|| | ||
Revision as of 15:55, 16 September 2013
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Isolate plasmid from overnight culture
- Using Omega mini prep kit protocol
- Samples:
- TODF 1,2,3,
- TODX 1, 2, 3
- TOBG 1, 2, 3,
- RFP 1, 2, 3
| sample | Volume (ul) | Concentration (ng/ul) |
| TODF1 | 43 | 120 |
| TODF2 | 43 | 98.8 |
| TODX1 | 42 | 399.3 |
| TODX2 | 44 | 442.2 |
| TODX3 | 43 | 417.5 |
| TOBG1 | 43 | 262.4 |
| TOBG2 | 47 | 319.2 |
| TOBG3 | 41 | 338.4 |
| RFP1 | 41 | 77.7 |
| RFP2 | 41 | 32.7 |
| RFP3 | 42 | 59 |
Glycerol stocks
- Took 750ul from overnight culture and centrifuged at full speed for ~2 minutes
- Supernatant was removed
- Pellet resuspended in 375ul of HMFM
- Samples were then frozen at -80
Gel Purification of the pGEM-T pasmid double digestions ran in the 11/09/13
The ge was purified by using the The Zymoclean Gel DNA recovery Kit and its protocol was followed.
Nanodrop Results
| Sample | Volume | Concentration (ng/ul) | 280/260 | 260/230 |
| TODX | 48.5 | 7.1 | 1.83 | 0.72 |
| TODF | 45.5 | 21.7 | 1.89 | 1.19 |
| TOBG | 47.7 | 9 | 1.77 | 0.70 |
| pSB1C3 (RFP) | 46.2 | 7.3 | 1.81 | 0.16 |
Digestion of the samples purified with the enzyme PstI-HF and XbaI
- Two single digestions were set up to test if one of the enzymes was not working properly.
| DNA volume | Volume | Cutsmart buffer | Enzyme volume | dH2O added to total volume of 60 ul |
| TODX | 23 | 6 | 1 | 30 |
| TODF | 22.5 | 6 | 1 | 30.5 |
| TOBG | 22 | 6 | 1 | 31 |
| pSB1C3 (RFP) | 20.5 | 6 | 1 | 32.5 |
Gel image of the above double digestion
Gel order: TODX, TODX, TODF, TODF, TOBG, TOBG, pSB1C3, pSB1C3 (XbaI); TODX, TODF, TOBG, pSB1C3 (PstI)
The picture above shows that the assumption that one of the enzymes did not working properly was wrong, as it shows the same result as the gel run on the 11/09/13.
Double digestion of the isolated pGEM plasmids ligated with the TOD operon genes (X, F and TOBG)
- As the digestions with the plasmids that were stored in the freezer did not work new digestins were set up with the isolated plasmids from the overnight culture.
- The pGEM-T plasmid contain the restrictions sites for PstI and SpeI, which are also present in the amplified TOD operon gene and the pSB1C3 plasmid.
- To avoid the recircularization of the pSB1C3 backbone when ligating the genes with this plasmid, the double digestion was set up with the enzymes PstI and XbaI.
- Another double digestion with EcoRI and SpeI was set up to test if the restrictions sites present in the TOD genes are not mutated. If the bands in the gel shows a linear band, it can be assumed that the enzymes cut the pGEM plasmids in its PstI and SpeI restriction sites.
Master Mix of the PstI/XbaI double digestion
- 30 ul of cut samart buffer
- 5 ul of PstI
- 5 ul of XbaI
- 58 ul of dH2O
- 9.8 ul of the master mix were added to each reaction.
- 2 ug DNA of each sample were digested.
Protocol
| Sample | DNA volume | dH2O added to the final volume of 30ul
TODXF1||16.5|| |
