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AUGUST: WEEK 3
August, 16th
Resuspension from iGEM 2010 Distribution Kit of <partinfo>BBa_J13002</partinfo> (Plate 1, Well 13B) and <partinfo>BBa_I13522</partinfo> (Plate 2, Well 8A).
Transformation (1 ul) of <partinfo>BBa_J13002</partinfo>, <partinfo>BBa_I13522</partinfo>, INTEIN, CREAM (Mr.Gene) into 100 ul of E. coli TOP10 home-made competent cells.
Transformation of 15-4C5 (1 ul) into in re-competentized E. coli TOP10 carrying <partinfo>BBa_T9002</partinfo>.
Transfomants were plated on LB+Amp 100 ug/ml agar plates, the last one on LB+Amp100+Cm12,5 agar plates and were let grow ON at 37°C.
August, 17th
All plates showed colonies.
Pick of <partinfo>BBa_J13002</partinfo>, <partinfo>BBa_I13522</partinfo>, INTEIN, CREAM, co-trasformed <partinfo>BBa_T9002</partinfo> and inoculum into 1 ml of LB+Amp, LB+Kan, LB+Cm, respectively, to make glycerol stocks. Falcons were than refilled for the minipreps of the following day.
Inoculum of I5, I26, <partinfo>BBa_K105012</partinfo>, <partinfo>BBa_B0034</partinfo>, I20M-1, I20A-1, I21M-3, I21-4, I21A-7, I0 for minipreps of the following day.
Cultures were diluted (5ul in 2ml LB+antibiotic) for TECAN test:
| I7-A | I8-5 D | I9-1
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| I10-B | I12-2 | A2
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| <partinfo>BBa_B0032</partinfo> | I144C5-T9002 | I164C5-T9002
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| I174C5-T9002 | I184C5-T9002 | I194C5-T9002
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| ENTERO4C5-T9002 | |
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Glycerol stock was prepared for ENTERO4C5-T9002.
August, 18th
Cultures were diluted (5ul in 2ml LB+antibiotic) for TECAN test:
| I7-A | I8-5 D | I9-1
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| I10-B | I12-2 | A2
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| <partinfo>BBa_B0032</partinfo> | I144C5-T9002 | I154C5-T9002
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| I164C5-T9002 | I174C5-T9002 | I184C5-T9002
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| I194C5-T9002 | ENTERO4C5-T9002 |
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Glycerol stock was prepared for I154C5-T9002.
The following cultures were miniprepped and quantified with Nanodrop:
- I26: 67,5 ng/ul
- <partinfo>BBa_K105012</partinfo>: 60,9 ng/ul
- <partinfo>BBa_B0034</partinfo>: 64,5 ng/ul
- <partinfo>BBa_F2620</partinfo>: 91,8 ng/ul
- I20M-1: 191,8 ng/ul
- I20A-1: 176,2 ng/ul
- I21M-3: 156,2 ng/ul
- I21-4: 76,3 ng/ul
- I0: 121,2 ng/ul
- INTEIN: 143,9 ng/ul
<partinfo>J13002</partinfo>: 31,9 ng/ul
and than digested as follows for four hours:
| Culture | Kind | Final reaction volume (ul) | DNA (ul) | H20 (ul) | Enzyme 1 | Enzyme 2 | Buffer H
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| I26 | Insert | 25 | 21,5 | 0 | 0,5 EcoRI | 0,5 SpeI | 2,5
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| <partinfo>BBa_K105012</partinfo> | Vector | 25 | 16,5 | 5 | 0,5 E | 0,5 S | 2,5
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| <partinfo>BB_B0034</partinfo> | Vector | 25 | 15,5 | 6 | 0,5 E | 0,5 S | 2,5
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| <partinfo>BB_F2620</partinfo> | Insert | 25 | 16,5 | 5 | 0,5 E | 0,5 S | 2,5
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| I20M-1 | Insert/Screening | 25 | 8 | 13,5 | 0,5 E | 0,5 S | 2,5
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| I20M-1 | Insert/Screening | 25 | 8 | 13,5 | 0,5 XbaI | 0,5 PstI | 2,5
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| I20A-1 | Insert/Screening | 25 | 13 | 8,5 | 0,5 E | 0,5 S | 2,5
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| I20A-1 | Insert/Screening | 25 | 13 | 8,5 | 0,5 X | 0,5 P | 2,5
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| I21-4 | Insert/Screening | 25 | 13 | 8,5 | 0,5 E | 0,5 S | 2,5
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| I21-4 | Vector | 25 | 13,1 | 8,4 | 0,5 E | 0,5 X | 2,5
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| I0 | Vector | 25 | 8,2 | 13,3 | 0,5 E | 0,5 XbaI | 2,5
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| INTEIN | Insert | 25 | 10,5 | 11 | 0,5 E | 0,5 S | 2,5
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| <partinfo>BB_J13002</partinfo> | Vector | 25 | 21,5 | 0 | 0,5 S | 0,5 P | 2,5
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Two medium gel were prepared and samples were loaded and gel run/cut.
IMG
IMG
All samples were correctly digested and run; both I20M-1 and I20A-1 are positive, so we decided to use I20M-1.
Gel extraction gave these results:
- I0 (E-X): 20,8 ng/ul
- <partinfo>BB_F2620</partinfo> (E-S): 13,5 ng/ul
- INTEIN (E-S): 6,5 ng/ul
- <partinfo>BB_B0034</partinfo> (E-X): 23,2 ng/ul
- I20M-1 (E-S): 7,4 ng/ul
- <partinfo>BB_J13002</partinfo> (S-P): 12,5 ng/ul
- I21-4 (E-S): 7,2 ng/ul
- I21-4 (E-X): 24,7 ng/ul
- <partinfo>BBa_K105012</partinfo> (E-X): 23,1 ng/ul
- I26 (E-S): 3,4 ng/ul
- I20M-1 (X-P): 6,5 ng/ul
They were stored ON at -20°C.
August, 19th
August, 20th
August, 21st
August, 22nd
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