*****For immediate use October 15, 2007
Tokyo, October 15, 2007 - NEC has developed the world's first portable human DNA Analyzer with Aida Engineering (headquartered in Sagami, Kanagawa Prefecture; President: Kimikazu Aida). This analyzer integrates all steps of the DNA analysis process, from DNA extraction to electrophoresis and individual profiling.
The analyzer has been developed mainly for the law enforcement market. By narrowing the analyzer's application to DNA analysis specifically for individual identification, developers have streamlined the analytical process and realized a compact device the size of an attaché case (500mm W x 400mm D x 200mm H) that can be easily transported and analyzed at crime scenes.
DNA analysis process consists of 5 steps: (1) cell collection, (2) DNA extraction, (3) Polymerase Chain Reaction (PCR) to amplify DNA fragments, (4) electrophoresis to ascertain DNA "fingerprints" and (5) STR analysis for determining genetic profiling. NEC's newly developed device is the world's first portable DNA analyzer to fully integrate the entire process.
The compact nature of the analyzer facilitates coordination between each step and greatly expedites the PCR procedure where DNA fragments are alternatively heated and cooled. As a result, the device can complete the entire process, from DNA extraction to analysis, in approximately 25 minutes.
NEC is confident that the analyzer will speed up criminal investigations and aid crime prevention efforts. The company will continue to make further improvements to the device and strengthen development activities in readiness for full-scale production in 2008.
The following is an outline of NEC's new DNA Analyzer for individual profiling.
1. Compact for improved portability
The use of miniaturized versions of PCR and electrophoresis equipment incorporating "lab-on-a-chip" technology, an innovation that replaces test tubes with a plastic chip, has resulted in the entire device being more compact. The use of "lab-on-a-chip" technology has emerged from the development of dedicated chips that feature multiple layers of silicon film laminated on a single layer of resin. Conventional PCR and electrophoresis equipment is typically the size of a small printer and compact refrigerator, respectively. In this new device, however, this equipment has been greatly miniaturized to approximately 10cm x 5cm x 5cm and 10cm x 5cm x 3cm.
2. High speed analysis in approximately 25 minutes
The compact nature of the analyzer facilitates coordination between each step in DNA analysis, resulting in faster processing. The speed of the new compact analyzer over larger devices is particularly evident during the PCR step.
Traditionally, DNA analysis required approximately one working day (one week when re-testing was required) and numerous devices to complete all necessary procedures. It was therefore difficult to make a quick shortlist of suspects using DNA analysis soon after a crime had occurred. This situation led to calls being made for a device that would provide quick DNA analysis at the scene of a crime. At the same time, the CODIS(*) database for storing DNA data on crime suspects and other individuals was under development in the U.S. and is presently utilized in criminal investigations. This trend towards data sharing has spread across the globe, with Japan also working to install a similar DNA database.
*Combined DNA Index System: presently holds data on approximately 4 million individuals
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1. | DNA Analysis Process (1) Cell Collection The cell collection is integral to DNA analysis. It is possible to collect cells from blood samples and/or oral swab (simple oral swab using a cotton bud). |
(2) DNA Extraction DNA is extracted from collected cells using special reagents. |
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(3) PCR (Polymerase Chain Reaction) Amplification The technique known as PCR(*) is used to amplify specific fragments of DNA to a number of copies that makes analysis possible. (*) DNA fragments are alternatively heated and cooled at fixed temperature intervals with special reagents. |
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(4) Electrophoresis Amplified DNA fragments are injected into a polymer gel. A high voltage is applied to the gel to move DNA molecules towards the anode. (This is because the DNA itself takes on a negative charge.) As the polymer is uniformly porous, DNA molecules meet resistance and travel through this matrix at different rates depending on the fragment size of each molecule. (The polymer forms a molecular sieve where smaller molecules move faster than larger molecules.) The principle of electrophoresis is used to measure the size of DNA fragment. |
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(5) STR (Short Tandem Repeat) Analysis The human genome has a number of unique genetic elements. These elements are formed when a DNA sequence, consisting of 4-5 of the nucleic acids that make up DNA (A/C/G/T), are repeated as a pattern. The number of repeated sequences may differ from person to person and it is the analysis of this repetition that enables genetic profiling. |
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Lab-on-a-chip Technology Lab-on-a-chip technology features wells and channels on a small plastic base chip, where each well is used an individual "test tube". With a diameter of around 5mm these well are much smaller than regular test tubes. The transfer of fluid across the wells is facilitated by the channels. This allows lab processes to be scaled down to a chip format without the need for regular fluid transfer tools (such as pipettes). |
All company and brand names used in this release are trademarks or registered trademarks of their respective owners.
Yoshibumi Yashiro |
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NEC Corporation +81-3-37986511 y-yashiro@bc.jp.nec.com |
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