PCR Amplification of DNA (Taken from Plant Biotech)
1. Thaw all components (except Taq Polymerase) on ice 30 min before the lab.
2. Combine the following components for each reaction (on ice) in an Eppendorf tube:
Tube (1.5 ml Eppendorf) |
Distilled water |
10X PCR buffer |
dNTP |
5 unit/µl Taq Polymerase |
Total |
Wizard Mix |
284 µl |
36 µl |
36 µl |
4 µl (ask TA to pipet enzyme) |
360 µl |
3. Vortex and centrifuge for 30 seconds at 13,000rpm.
4. Combine the following for each reaction in a PCR tube(50 ul total reaction volume).
Tube |
Wizard Mix |
DDH20 |
A plasmid containing hsp16.6 gene |
Cyanobacterium genomic DNA |
A plasmid containing cox II gene |
Onion genomic DNA |
Primers (F and R) for hsp16.6 gene |
Primers (F and R) for Cox II gene |
1 (Negative control) |
47 µl |
1 µl |
1 µl primer Fh 1 µl primer Rh |
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2 hsp16.6 gene control |
47 µl |
1 µl |
1 µl primer Fh 1 µl primer Rh |
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3 hsp16.6 gene |
47 µl |
1 µl |
1 µl primer Fh 1 µl primer Rh |
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4 (Negative control) |
47 µl |
1 µl |
1 µl primer Fc 1 µl primer Rc |
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5 cox gene control |
47 µl |
1 µl |
1 µl primer Fc 1 µl primer Rc |
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6 cox gene |
47 µl |
1 µl |
1 µl primer Fc |
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7 Positive control |
47 µl |
PUC18 plasmid provided in the kit 1 ml |
PUC18 primers provided in the kit 1 ul F +1 ul R = 2 µl total |
. Run the following program (about 2.5 h):
Initial Step
Next 30 cycles:
Program a final extension at
5. Take 10 µl of PCR product from each tube for gel electrophoresis (Refer to the protocol for agarose gel electrophoresis).
Materials:
sterile water
10X amplification buffer with 15mM MgCl2
10 mM dNTP
50 µM oligonucleotide primer F (forward)
50 µM oligonucleotide primer R (reverse)
5 unit/µl Taq Polymerase
template DNA (1 µg genomic DNA, 0.1-1 ng plasmid DNA) in ddH20
Text iGenetics by Peter J. Russell
This web site is provided for instruction in Botany and Zoology 342
by Kenneth G. Wilson,
Professor of Botany
Miami University
wilsonkg@muohio.edu