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Development of a Method for Producing Defined Surface Roughness of an Fe-Cr-Al-Y Substrate. Different methods for introducing a controlled surface roughness onto a Fe-Cr-Al-Y sample surface were explored. Roughness with a wavelength of l = 20-100 mm and up to 10 mm amplitude were sought. Ion milling and chemical etching were both used as means of material removal. Physically attached grids of different size and holographically-etched photoresist were used to selectively cover portions of the substrate surface during ion milling. Alternatively, niobium and silicon dioxide, deposited onto the substrate through a grid mask were used to protect the substrate during chemical etching. A maximum of 2-micron roughness was achieved using ion milling, while 4-micron roughness was achieved using chemical etching.
Figure 1 shows a simple schematic of gene therapy, where we take cationic lipids, used as the nonviral vector, to introduce the foreign DNA into a cell. Once the CL/DNA complex has passed through the cellular membrane, we hope that the DNA is broken free from the complex and released in the cell. The DNA will then pass through the nuclear membrane into the nucleus, which will eventually be transcribed into RNA and then expressed into protein. My part of the project was primarily focused on the process of transfection alone (points 1-2). Although I briefly learned the techniques to study the expression of DNA during the summer, I focused on studying the images taken from transfection. Another intern in the research group focused on how much protein was expressed from foreign DNA (points 3-4). Return to the RISE 2000 project list |
