Team:UNIPV-Pavia/Calendar/June/settimana5

From 2011.igem.org

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For each of them 1 ul was transformed in 100 &mu;l of <i>home-made</i> TOP10 competent cells.
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For each of them 1 &mu;l was transformed in 100 &mu;l of <i>home-made</i> TOP10 competent cells.
Transformants were plated on LB agar plates with the right antibiotic and incubated ON at 37°C.
Transformants were plated on LB agar plates with the right antibiotic and incubated ON at 37°C.
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</p>

Revision as of 14:57, 16 July 2011

UNIPV TEAM 2011

March
M T W T F S S
  1 2 3 4 5 6
7 8 9 10 11 12 13
14 15 16 17 18 19 20
21 22 23 24 25 26 27
28 29 30 31    

April
M T W T F S S
        1 2 3
4 5 6 7 8 9 10
11 12 13 14 15 16 17
18 19 20 21 22 23 24
25 26 27 28 29 30

May
M T W T F S S
            1
2 3 4 5 6 7 8
9 10 11 12 13 14 15
16 17 18 19 20 21 22
23 24 25 26 27 28 29
30 31

June
M T W T F S S
    1 2 3 4 5
6 7 8 9 10 11 12
13 14 15 16 17 18 19
20 21 22 23 24 25 26
27 28 29 30

July
M T W T F S S
        1 2 3
4 5 6 7 8 9 10
11 12 13 14 15 16 17
18 19 20 21 22 23 24
25 26 27 28 29 30 31

August
M T W T F S S
1 2 3 4 5 6 7
8 9 10 11 12 13 14
15 16 17 18 19 20 21
22 23 24 25 26 27 28
29 30 31

September
M T W T F S S
      1 2 3 4
5 6 7 8 9 10 11
12 13 14 15 16 17 18
19 20 21 22 23 24 25
26 27 28 29 30

October
M T W T F S S
          1 2
3 4 5 6 7 8 9
10 11 12 13 14 15 16
17 18 19 20 21 22 23
24 25 26 27 28 29 30
31

JUNE: WEEK 5

June, 28th

First time in wet lab

11 LB agar plates, 35 LB agar + Amp plates and 15 LB agar + Cm 12.5 were prepared.

  • <partinfo>BBa_C0060</partinfo> was resuspended from iGEM 2011 kit distribution, Plate 1, well 4K in 15 μl of ddH2O
  • <partinfo>BBa_C0061</partinfo> was resuspended from iGEM 2011 kit distribution, Plate 1, well 4M in 15 μl of ddH2O
  • <partinfo>BBa_J04450</partinfo> was resuspended from iGEM 2011 kit distribution, Plate 1, well 5E in 15 μl of ddH2O
  • <partinfo>BBa_K081022</partinfo> was resuspended from iGEM 2011 kit distribution, Plate 2, well 12N in 15 μl of ddH2O

For each of them 1 μl was transformed in 100 μl of home-made TOP10 competent cells. Transformants were plated on LB agar plates with the right antibiotic and incubated ON at 37°C.

June, 29th

In the morning all plates showed colonies (<partinfo>BBa_J04450</partinfo> showed light red colonies); for each one we picked one colony and inoculated it in 1 ml of liquid LB with the proper antibiotic (ampicillin for <partinfo>BBa_C0060</partinfo>, <partinfo>BBa_C0061</partinfo> and <partinfo>BBa_K081022</partinfo>, kanamycin for <partinfo>BBa_J04450</partinfo>). Cultures were grown at 37°C, 220 rpm.

In the afternoon glycerol stocks were prepared (750 μl of bacteria and 250 μl of 80% glycerol) and stored at -80°C except for <partinfo>BBa_C0061</partinfo> which was not sufficiently grown (we let it grow until next morning); then cultures were refilled with 5 ml of liquid LB with the proper antibiotic and incubated ON at 37°C, 220 rpm.

June, 30th

All cultures were saturated; glycerol stock for <partinfo>BBa_C0061</partinfo> was prepared and stored at -80°C.

Plasmids were extracted with MiniPrep kit; purified DNA was quantified with NanoDrop Spectrophotometer:

DNA ng/μl
<partinfo>BBa_C0060</partinfo> 60.8
<partinfo>BBa_C0061</partinfo> 75.7
<partinfo>BBa_K081022</partinfo> 63.6
<partinfo>BBa_J04450</partinfo> 17.5

<partinfo>BBa_B0030</partinfo>, <partinfo>BBa_B0031</partinfo>, <partinfo>BBa_B0032</partinfo>, <partinfo>BBa_B0034</partinfo>, <partinfo>BBa_B0015</partinfo>, <partinfo>pSB4C5</partinfo>, <partinfo>BBa_I13501</partinfo>, <partinfo>BBa_I13507</partinfo> were inoculated from freezer glycerol stocks and grown ON at 37°C, 220 rpm for MiniPrep.