PCR mgtc, hly

Kamila

Tasks:

• Amplification of hly

Methods:

• PCR mixture's composition:

  2,5ul pfu buffer (Fermentas), 2,5ul MgSO4 (Fermentas), 1,5ul primers, 1,5ul dNTPs (10 mM), 01,ul pfu turbo polymerase (Fermentas), 1ul template DNA from Listeria, solution was topped up with H2O to 25ul.

  1 repeat of every sample was made (2 different programs).

  Additionally for each sample was made version with 10X dilution of template.

• PCR programs:

hly

4min 95°C 
 (30s 95°C, 35s 42°C, 1min20s 72°C)x3 
 (30s 95°C, 35s 47°C, 1min20s 72°C)x28 
 10min 72°C 
 ~ 7°C

random program

• Electrophoretic separation on 1% agarose gel

Results:

Notes:

• Inappropriate template DNA was used for mgtc (ganomic DNA from Yersinia instead of genomic DNA from Listeria).