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AUGUST: WEEK 1
August, 2nd
Miniprep and quantification at Nanodrop of:
- I20-1: 98,2 ng/ul
- I20-2: 63,6 ng/ul
- I20-3: 41,5 ng/ul
- I21-1: 45 ng/ul
- I21-2: 45 ng/ul
- I21-3: 54 ng/ul
These samples were prepared and sent (400ng) to BMR Genomics for sequencing.
The following parts were resuspended from iGEM 2010 Distribution Kit:
- <partinfo>BBa_R0062</partinfo> (Plate 1, Well 6O)
- <partinfo>BBa_K081008</partinfo> (Plate 2, Well 10N)
both in vector <partinfo>pSB1A2</partinfo>.
Transformation (1ul) of the following parts (resuspended/already miniprepped):
| Part | Strain
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| pAH123 | MC1061
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| MG1655
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| <partinfo>BBa_J72008</partinfo> | MC1061
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| MG1655
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| <partinfo>BBa_R0062</partinfo> | DH5-alpha
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| <partinfo>BBa_K081008</partinfo> | DH5-alpha
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Transformed cells were plated on proper LB+Amp agar plates and grown ON at right temperature:
| Part | Plate resistance | Temperature
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| pAH123 | Amp 50 ug/ml | 30°C
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| <partinfo>BBa_J72008</partinfo>
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| <partinfo>BBa_R0062</partinfo> | Amp 100 ug/ml | 37°C
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| <partinfo>BBa_K081008</partinfo>
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August, 3rd
Check for plates grown ON: all plates showed colonies.
A single colony was picked from <partinfo>BBa_R0062</partinfo> and <partinfo>BBa_K081008</partinfo> plates and inoculated in 1 ml LB+Amp 100 ug/ml and incubated 37°C, 220 rmp for glycerol stock.
Imgs
Since plates left showed small colonies they were let grow until late afternoon; than single colonies were picked and inoculated into 5 ml LB+Amp 50 ug/ml and incubated ON at 37°C, 220 rpm.
Imgs
PCR from the following colonies (this is a test to check the efficiency of primers and it will be our negative control for E. coli integration screenings):
- MC1061-1
- MC1061-2
- MG1655-1
- MG1655-2
- Blank (Nothing)
using our primers synthesized to check attPhi80 E. coli genomic integration.
August, 4th
August, 5th
August, 6th
August, 7th
August, 8th
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