Team:UNIPV-Pavia/Calendar/August/settimana1

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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
pAH123 MC1061
MG1655
<partinfo>BBa_J72008</partinfo> MC1061
MG1655
<partinfo>BBa_R0062</partinfo> DH5-alpha
<partinfo>BBa_K081008</partinfo> DH5-alpha

Transformed cells were plated on proper LB+Amp agar plates and grown ON at right temperature:

Part Plate resistance Temperature
pAH123 Amp 50 ug/ml 30°C
<partinfo>BBa_J72008</partinfo>
<partinfo>BBa_R0062</partinfo> Amp 100 ug/ml 37°C
<partinfo>BBa_K081008</partinfo>

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

Calendar

August

week 1

week 2

week 3

week 4

week 5