Preimplantation genetic diagnosis (PGD) is an alternative to prenatal diagnosis for ensuring the genetic health of offspring born to families affected by inherited disease. This paper sets out to review current protocols for the diagnosis of single gene defects in human preimplantation embryos. Thes
Strategies for enhancing the speed and integration of microchip genetic amplification
β Scribed by Viet N. Hoang; Govind V. Kaigala; Alexey Atrazhev; Linda M. Pilarski; Christopher J. Backhouse
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 230 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0173-0835
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
In this work, we explore the use of methods that allow a significant acceleration of genetic analysis within microchips fabricated from low thermal conductivity materials such as glass or polymers. Although these materials are highly suitable for integrating a number of genetic analysis techniques onto labβonβaβchip devices, their low thermal conductivity limits the rate at which heat can be transferred and hence lowers the speed of thermal cycling. However, short thermal cycling times are the key to bringing PCR to clinical pointβofβcare applications. Although shrinking the PCR reaction chamber volume can increase the speed of thermal cycling, this strategy is not always suitable, particularly when dealing with clinical samples with low analyte concentrations. In the present work, we combine two alternate strategies for decreasing the time required to perform PCR: implementing a heat sink and optimizing the PCR protocol. First, the heat sink substantially reduces the thermal resistance opposing heat dissipation into the ambient environment, and eliminates the parasitic thermal capacitance of the regions in the microchip that do not require heating. The low thermal conductivity of glass is used to our advantage to design the heatβsink placement to achieve fast thermal transitions while maintaining low power consumption. Second, we explore the application of twoβstage PCR to provide a further reduction in the time required to perform genetic amplification by merging the annealing and extension stages of the commonly used threeβstage PCR approach. In combination, we reduce the time required to perform thermal cycling by roughly a factor of 3 while improving the temperature control.
π SIMILAR VOLUMES
## Abstract An integrated system of a siliconβbased microfabricated polymerase chain reaction (ΞΌPCR) chamber and microfabricated electrophoretic glass chips have been developed. The PCR chamber was made of silicon and had aluminum heaters and temperature sensors integrated on the glass anodically b
## Abstract Azadirachtin is considered as the best pesticide among the biopesticides available in market for crop protection due to its broad spectrum activity and varying mode of action. To meet the increasing demand and primarily due to geographical and variability limitations, its biotechnologic