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Titlebook: BioMEMS and Biomedical Nanotechnology; Volume II: Micro/Nan Mauro Ferrari (Editor-in-Chief, Professor, Brown I Book 2007 Springer-Verlag US

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發(fā)表于 2025-3-21 18:24:08 | 只看該作者 |倒序瀏覽 |閱讀模式
期刊全稱BioMEMS and Biomedical Nanotechnology
期刊簡稱Volume II: Micro/Nan
影響因子2023Mauro Ferrari (Editor-in-Chief, Professor, Brown I
視頻videohttp://file.papertrans.cn/187/186420/186420.mp4
發(fā)行地址Focuses on diagnostic and therapeutic applications of MEMS and nanotechnology in biomedical engineering.Heavily illustrated with line drawings, half tones and many color illustrations.Top researchers
圖書封面Titlebook: BioMEMS and Biomedical Nanotechnology; Volume II: Micro/Nan Mauro Ferrari (Editor-in-Chief, Professor, Brown I Book 2007 Springer-Verlag US
Pindex Book 2007
The information of publication is updating

書目名稱BioMEMS and Biomedical Nanotechnology影響因子(影響力)




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沙發(fā)
發(fā)表于 2025-3-21 23:55:08 | 只看該作者
https://doi.org/10.1057/9781137505385tes a sensing scheme based on cell based sensors. This technique is based on the development of single cell arrays that are used as biosensors that show parts per billion sensitivity and have the capability of identifying specific chemical analytes based on unique electrical identification tags also
板凳
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https://doi.org/10.1057/9781137505385 be selectively positioned by their dielectric properties. An almost unlimited variety of molecules and nanocomponents can be utilized with these devices, including: DNA, DNA constructs with fluorescent, photonic or electronic transfer properties, RNA, RNA constructs, amino acids, peptides, proteins
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https://doi.org/10.1007/978-1-4614-6151-7llular analysis [., ., .]. Advantages of these μ-TAS over bench-top instruments include low reagent consumption, small sample volumes, high separation efficiencies, short reaction times, ease of automation, and potential for massproduction with low cost [.].
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Gene Expression Profiling Utilizing Microarray Technology and RT-PCRes for gene expression analysis, the subject of this review, has lagged behind analysis of genetic variation, primarily due to the intrinsic complexity of gene expression measurement. However, the number of studies employing gene expression analysis has expanded in the last few years as the availabl
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From One-Bead One-Compound Combinatorial Libraries to Chemical Microarrayss were probed with fluorescent-labeled antibodies, and quantitated with a fluorescent scanner. About the same time, we described the use of split-mix synthesis method to generate millions of random peptide-beads such that each bead displayed only one peptide entity [.]. These “one-bead one-compound”
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