PCR Qualitative Analysis
[ PCR Procedures | Quantative PCR Analysis
| Detection Limit & Quantification Limit
]
Qualitative PCR tests a sample for the presence or absence of particular
DNA sequences indicative for the presence of genetically modified
materials.
A screening test uses element specific primers that target the
DNA sequences of genetic elements commonly used in genetic engineering
of crops. These sequences are present in the sections of foreign,
recombinant DNA of many different GMOs. In this way, a sample can
be screened for the presence of multiple genetic modifications using
only one or two general primer systems. For example, all currently
approved (in the US) genetic modifications in soybeans contain the
35S promoter. A qualitative screening test on a soybean sample that
targets the 35S promoter will detect whether GM soy material is
present, but it cannot be used to determine which of the specific
genetic modifications is present.
A modification specific test can detect and identify a particular
GM construct through the use of primers that target a DNA sequence
unique to this specific genetic modification. For example, primers
used to specifically detect Roundup Ready soybean target the junction
between the 35S promoter from Cauliflower Mosaic Virus and the chloroplast
transit peptide from petunia. This artificially juxtaposed DNA sequence
is found neither in nature nor in any other GMO. Its detection thereby
gives very high confidence of the presence of Roundup Ready soy.
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