Overview: Polymerase Chain Reaction (PCR), invented by Kary B. Mullis, at the Cetus Corporation, who was awarded the 1993 Nobel Prize for chemistry for PCR, is a technique to exponentially amplify in vitro a small quantity of a specific nucleotide sequence in the presence of template sequence, two oligonucleotide primers that hybridize to opposite strands and flank the region of interest in the target DNA, a thermostable (taq) DNA polymerase. The reaction is cycled involving template denaturation, primer annealing, and the extension of the annealed primers by DNA polymerase until enough copies are made for further analysis.
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Protocols
- Home-Made Taq Polymerase Purification (Dr. Simon Dawson, Department of Biochemistry, University of Nottingham Medical School)
Taq polymerase can be expensive. Here is the protocol for making your own Tag polymerase and it gives stable results.
http://www.nottingham.ac.uk/~mbzspd/methods/Home_m...
Added: Sat Apr 10 2004, Hits: 4061, Reviews: 0 Write review Cached - Interactive guide for solving common PCR-problems (Roche Diagnostics Corporation)
Troubleshooting hints based on the five most common symptoms observed: No product / Misincorporation or low fidelity / Non-specific bands / Smeared bands/Low yield.
http://www.roche-applied-science.com/pcr/applicati...
Added: Sat Sep 21 2002, Hits: 4691, Reviews: 0 Write review Cached - PCR Primer Design and Reaction Optimization (Ed Rybicki, Department of Molecular and Cell Biology, University of Cape Town)
A must read before you design a primer and run a PCR. This page covers almost every theoretical and practical aspects of PCR primer disign.
http://www.mcb.uct.ac.za/pcroptim.htm
Added: Sun Jan 23 2005, Hits: 6695, Reviews: 0 Write review Cached - Quantitative RT-PCR and Other PCR Procedures (Jack Vanden Heuvel, Penn State University)
A must-read protocol for PCR beginners as well as verterans. It touches in depth aspects specific to quantitative RT-PCR as well as those common to standard PCR.
http://www.cas.psu.edu/docs/CASDEPT/VET/jackvh/jvh...
Added: Sun Mar 28 2004, Hits: 15325, Reviews: 0 Write review -
Calculating Concentrations for PCR
(Molecular Biology Techniques Manual)
How to calculate primer and nucleotide concentration
http://www.mcb.uct.ac.za//pcrconcn.htm
Added: Tue May 14 2002, Hits: 6126, Reviews: 0 Write review Cached -
Guidelines for Determining the Number of PCR Cycles
(Qiagen)
http://www1.qiagen.com/resources/info/guidelines_f...
Added: Sun Jul 21 2002, Hits: 2240, Reviews: 0 Write review Cached -
PCR reaction components
(Roche Diagnostics Corporation)
Very useful introduction to PCR componets including template, primers, dNTP, additive, polymerase, pH, and MgCl2 concentration.
http://www.roche-applied-science.com/pcr/applicati...
Added: Sat Sep 21 2002, Hits: 3579, Reviews: 0 Write review Cached -
Preventing carry-over contamination with uracil-DNA glycosylase
(Roche Diagnostics Corporation)
PCR can amplify a single molecule over a billionfold. Thus, even minuscule amounts of a contaminant can be amplified and lead to a false positive result. Such contaminants are often products from previous PCR amplifications (carry-over contamination). One common strategy to avoid such contamination is substituting dUTP for dTTP during PCR amplification, to produce uracil-containing DNA (U-DNA).
http://www.roche-applied-science.com/pcr/applicati...
Added: Sat Sep 21 2002, Hits: 788, Reviews: 0 Write review Cached -
Setting up the laboratory to avoid contamination
(Roche Diagnostics Corporation)
The ability of the Polymerase Chain Reaction to amplify a single molecule means that trace amounts of DNA contaminants could serve as templates, resulting in amplification of the wrong template (false positives). This guide describes the common sources of contamination such as lab facilities and sample handling, and how to avoid contamination.
http://www.roche-applied-science.com/pcr/applicati...
Added: Sat Sep 21 2002, Hits: 1598, Reviews: 0 Write review Cached -
Thermal Cycling Profile for Standard PCR
(Roche Diagnostics Corporation)
Basic guide to PCR cycling and how to optimize each step.
http://www.roche-applied-science.com/pcr/applicati...
Added: Sat Sep 21 2002, Hits: 1818, Reviews: 0 Write review Cached
Trouble Shootings and FAQs
- PCR troubleshooting - smear and no clear band
- PCR contamination in negative control
- How to amplify GC-rich region?
- Reamplification got smear, what's wrong?
- After 30 cycles I don't see any more amplification - Taq dies too soon?
- Tips on using dUTP in PCR
- Amplifying DNA extracted from serum samples, are there PCR inhibitors in serum?
- How to decide the annealing temperature for PCR
- PCR contamination problem - how to set up a negative control?
- My PCR did not work again-
- Troubleshooting smearing on gel
- Tips on PCR Contamination problem
- How to get rid of PCR primer dimer?
- How to remove PCR inhibitors from DNA?
- Primer dimers- what exactly are primer dimers?
- Influence of MgCl2 on PCR
- My PCR does not work always
- How to safeguard dNTPS?
- How to optimize PCR conditions?
- Optimization of PCR annealing temperature
- Troubleshooting PCR contamination