Selected BioBricks:

Franek

Task:

• Alkaline lysis of the plasmid containing BBa_I0500
• Transform competent cells with BBa_B0024
• Second attempt to transform competent cells with BBa_I0500

Methods:

• Plates with BBa_I0500 were empty, therefore once again transformation of chemocompetent cells was performed, but this time 8µl of BBa_I0500 DNA solution was used
• Plating bacterias with BBa_I0500 on LB medium supplemented with kanamycin
• Resuspension of DNA from plate 1, 2C (BBa_B0024) with 15µl of H2O
• Transformation of chemocompetent cells with 4µl of BBa_B0024 DNA solution
• Plating bacterias with BBa_B0024 on LB medium supplemented with ampicillin

Results:

• Will be determined tomorrow

Jarek

Task:

• Isolation of plasmid containing parts from liquid cultures
• Digestion of acquired samples with restriction endonucleases
• Electrophoretic separation of digested samples
• Isolation of samples from agarose gel

Methods:

• Plasmid DNA was isolated with A&A "Plasmid Mini" kit, the DNA concentration was measured with nanodrop
• For digestion 1 ul of PstI/SpeI (B0032) or PstI/XbaI enzymes and 2 ul of 1xTango buffer were used. Digestion was held for 3 hours.
• After digestion samples were separated due to elecrophoresis in 0,8 agarose gel in TBE buffer
• Samples were isolated from gel with A&A "Gel-out" kit

Results:

Cloning the p53 coding sequence

Marcin

Comment:

Because of completely degradation of PCR product there is urgent need to amplified the p53 coding sequence. I think the original plasmid with the p53 is preserved and I'm about to repeat the PCR reaction using the plasmid as the matrix.

Tasks:

• Prepare PCR reaction to amplified p53 coding sequence.

Methods:

• PCR mixture composition:

1. proper mixture: 0.25 ul primer 1 (50 nM; Oligo.pl), 0.25 ul primer 2 (50 nM; Oligo.pl), 1.5 ul DNTPs (20 uM ;Fermentas), 0.5 ul Pfu turbo polymerase (KNGiE), 2.5 ul Pfu Turbo Buffer (Fermentas), 2.5 ul MgSO₄ (20 uM; Fermentas), 1 ul DNA matrix, 16.5 ul MQ water
2. Negative control: the same as previously described proper mixture, the only distinction is lack of the DNA matrix.

• Program:

p53

1. 98°C - hold
2. 98°C - 2 minutes
3. 98°C - 15 sec
4. 64°C - 30 sec
5. 68°C - 2 minutes
   go to 2 until number of cycles=35
6. 68°C - 10 minutes
7. 4°C - hold

After PCR the reaction was divided to 3 portion and loaded into the agarose gel to photograph and subsequently gel-out the sample

Gel with the PCR product and negative control of the reaction

Comment:

The effectiveness of PCR reaction was surprisingly low, probably due to degradation of the DNA matrix. Reamplification of the p53 sequence using the purificated DNA sample from the gel seems to be a good idea. Of course sometimes reamplification lead to obtain partially degraded sequences but I think I should try this method.