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This microfluidic chip is designed to perform chemical cell lysis. Suspended cells and an lysing buffer would be mixed inside the cell. This mixture of buffer and cells would be then mixed with a neutralization buffer to prevent DNA degradation. The mixture would then move to the diamond chamber where the DNA binds magnetic particles. Lastly, an elution buffer would be input and to clean and release the DNA from the magnetic particles. | This microfluidic chip is designed to perform chemical cell lysis. Suspended cells and an lysing buffer would be mixed inside the cell. This mixture of buffer and cells would be then mixed with a neutralization buffer to prevent DNA degradation. The mixture would then move to the diamond chamber where the DNA binds magnetic particles. Lastly, an elution buffer would be input and to clean and release the DNA from the magnetic particles. | ||
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+ | Note that the control layer is used as a region to mill a space on the opposite side of the flow layer for an electro-magnet to be implemented. | ||
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Revision as of 00:23, 31 October 2017
![](https://static.igem.org/mediawiki/2017/0/02/MARSbackground.png)
![](https://static.igem.org/mediawiki/2017/2/22/MARSLogo2.png)
![](https://static.igem.org/mediawiki/2017/3/33/MARS_Cell_Lysis.png)
Summary
Cell lysis is a commonly used protocol in synthetic biology. It can be performed through a variety of different methods, however we had focused on chemical cellular lysis. Cell Lysis is used to extract and isolate DNA from a specific type of cell. This is an extremely important step in building genetic circuits in order to utilize specific coding regions in a cell's DNA. Chemical cell lysis involves introducing cells to a series of buffers in order to degrade the cell’s outer membrane and collect the DNA that is released.
This microfluidic chip is designed to perform chemical cell lysis. Suspended cells and an lysing buffer would be mixed inside the cell. This mixture of buffer and cells would be then mixed with a neutralization buffer to prevent DNA degradation. The mixture would then move to the diamond chamber where the DNA binds magnetic particles. Lastly, an elution buffer would be input and to clean and release the DNA from the magnetic particles.
Note that the control layer is used as a region to mill a space on the opposite side of the flow layer for an electro-magnet to be implemented.
This chip has been milled, tested and deemed fully fluid functional. For a more complete understanding of the chip, click the download button in order to access its CNC millable SVG files, JSON file, full device documentation and PNG files of its flow and control layers.
Note that the control layer is used as a region to mill a space on the opposite side of the flow layer for an electro-magnet to be implemented.
This chip has been milled, tested and deemed fully fluid functional. For a more complete understanding of the chip, click the download button in order to access its CNC millable SVG files, JSON file, full device documentation and PNG files of its flow and control layers.
![Picture](https://static.igem.org/mediawiki/2017/b/bb/MARS_Lysis_F.png)
![Picture](https://static.igem.org/mediawiki/2017/0/00/MARS_Lysis_C.png)
![Picture](https://static.igem.org/mediawiki/2017/0/08/MARS_Lysis_M.png)
![Picture](https://static.igem.org/mediawiki/2017/0/00/MARS_Lysis_C.png)
Testing
This following video shows a test of the chip using colored water. This is to show help explain the functionality of the chip.
No biological material was inserted into this chip.