Crime Scene Investigator PCR Basics Real-Time PCR Starter Kit

Run your DNA gels in 10 minutes!

Find Out How

Designed to teach the basics of real-time quantitative PCR in the classroom, this kit includes the components of the Crime Scene Investigator PCR Basics Kit and adds the reagents, consumables, and instructions needed to perform the same analysis using real-time PCR. Given the robustness of the Crime Scene Investigator PCR Basics Kit and the expense of the real-time PCR reagents, this kit is a good starting point for novices to become familiar with real-time PCR techniques. Real-time PCR is useful in food analysis, gene expression analysis, and many other applications in which the goal is to not only ask “what DNA is present” but also “how much".

Since genotyping rather than quantitation is the goal for DNA fingerprinting, real-time PCR is not used in the real-world STR analysis that the Crime Scene Investigator Kit simulates. However, the real-time PCR application that this kit offers is a rich opportunity to learn the principles and techniques of real-time quantitative PCR. Additionally, the DNA fingerprints can still be investigated using gel electrophoresis and melt-curve analysis showing how real-time and conventional PCR can be complementary techniques.
The laboratory is performed without the need for complex genomic DNA extraction steps.

With this kit, students are able to:

• Perform real-world DNA profiling
• Discover key differences between conventional and real-time PCR analysis
• Analyze and evaluate real-time PCR results
• Perform melt curve analysis
• Visualize results using agarose gel electrophoresis

Features and Benefits

• Two–session laboratory activity, 45 min per session
• Provides sufficient materials for eight student workstations, up to four students per workstation
• Includes curriculum with Teacher's Guide, Student Manual, and graphical Quick Guide

How It Works

DNA profiling determines the exact genotype of a DNA sample, distinguishing one human being from another by identifying each person's unique DNA "bar code." This powerful tool aids investigations of crime scenes, missing persons, mass disasters, immigration disputes, and paternity. Crime scenes often contain tiny biological specimens (blood, semen, hairs, saliva, bones, pieces of skin) from which DNA can be extracted. The reason DNA profiling is so useful for forensic scientists is that a definitive DNA profile can be obtained from a minute biological sample using the power of DNA amplification afforded by polymerase chain reaction (PCR).

There are ~3 billion bases in the human genetic blueprint, and more than 99.5% of them do not vary among human beings. Within the variant areas of the genome are the special polymorphic ("many forms") sequences used in forensic applications. The DNA sequences used for forensic typing are derived from regions of our chromosomes that do not control any known traits and have no known functions. They contain segments of short tandem repeats, called STRs. STRs are very short DNA sequences that are repeated in direct head-to-tail fashion.

The example below shows a locus (known as TH01) actually used in forensic DNA profiling. Its specific DNA sequence contains five repeats of [TCAT]

For the TH01 STR locus, there are many alternate forms (alleles) that differ from each other by the number of [TCAT] repeats present in the sequence. More than 20 different alleles of TH01 have been discovered in people worldwide. Each of us still has only two alleles, one inherited from our mother and one inherited from our father.

Two sample TH01 genotypes

Each STR allele has a different length depending on the number of tandem repeats it contains. When the alleles are amplified by PCR, alleles of different lengths can be distinguished by electrophoresis. The number of tandem repeats contained in each allele can be determined by comparing the locations of the DNA bands with a DNA size standard that corresponds to the known sizes of TH01 alleles. In real crime scene applications, using the international CODIS system, DNA profiling is performed using 20 loci to increase the power of discrimination. With the addition of each locus to the analysis, the possibility that any two genotypes will match due to chance drops off significantly. This exercise allows students to grasp the concept of the power of discrimination — the more loci that are used, the greater the ability to discriminate between any two samples.