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Team:UNIPV-Pavia/Notebook/Week4Jul
From 2009.igem.org
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*We decided to perform gel run/cut/purification for MRGENE2 and for B0030, while we decided to perform DNA precipitation with sodium acetate for MRGENE1. | *We decided to perform gel run/cut/purification for MRGENE2 and for B0030, while we decided to perform DNA precipitation with sodium acetate for MRGENE1. | ||
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| + | *We transformed about 2.5 pg of A14-4 in TOP10 in order to filter the wanted plasmids. We plated the transformed bacteria and incubated the plates at 37°C overnight. | ||
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| + | *We infected 5 ml of LB + Amp with 10 ul of A12-2 and A12-3 glycerol stocks. Tomorrow they will be miniprepped and sent to sequence! | ||
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Revision as of 20:06, 20 July 2009
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Week from July 20th, to July 26th, 2009
Previous Week
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Next Week
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July, 20th
- Overnight digestion (20 ul reaction volume) for:
| MRGENE1(X-P) | MRGENE1-2(X-P) | MRGENE1-3(X-P) |
| MRGENE2(X-P)(X2) | MRGENE2-2(X-P) | MRGENE2-3(X-P) |
| B0030(S-P)(X3) |
- NOTE: reactions which involve excision(X-P) were performed on 3 ug of DNA, while S-P digestions were performed with 1 ug of DNA. We decided to have 3 replicates to be sure to have an acceptable yield.
- We decided to perform gel run/cut/purification for MRGENE2 and for B0030, while we decided to perform DNA precipitation with sodium acetate for MRGENE1.
- We transformed about 2.5 pg of A14-4 in TOP10 in order to filter the wanted plasmids. We plated the transformed bacteria and incubated the plates at 37°C overnight.
- We infected 5 ml of LB + Amp with 10 ul of A12-2 and A12-3 glycerol stocks. Tomorrow they will be miniprepped and sent to sequence!
July, 21st
July, 22nd
July, 23rd
July, 24th
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Previous Week
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Next Week
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