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- Jing Nan
- Department of Computer and Electrical Engineering, Texas A&M University
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- Kameoka Jun
- Department of Computer and Electrical Engineering, Texas A&M University
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- Su Chin B.
- Department of Computer and Electrical Engineering, Texas A&M University
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- Chou Chao-Kai
- Department of Molecular and Cellular Oncology, University of Texas
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- Hung Mien-Chie
- Department of Molecular and Cellular Oncology, University of Texas
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In this letter, detection of target protein molecules has been demonstrated by a two-dimensional (2D) photon burst analysis technique and microfluidic channel device. Individual molecule events are scatter plotted in terms of their photon counts and burst width in 2D photon burst analysis. Detection of target protein is verified by a higher counts-per-bin for rabbit anti-HA polyclonal antibody sample than that of the control sample from the 2D photon burst analysis. Since this is microfluidic single molecule detection scheme, it has the advantages of high sensitivity, small sample consumption and reduced processing time, comparing to the conventional immunological ensemble measurements, such as western blot, immuno-precipitation, etc.
収録刊行物
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- Journal of Photopolymer Science and Technology
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Journal of Photopolymer Science and Technology 21 (4), 531-536, 2008
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詳細情報 詳細情報について
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- CRID
- 1390001204324096000
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- NII論文ID
- 130004464678
- 40016109018
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- NII書誌ID
- AA11576862
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- COI
- 1:CAS:528:DC%2BD1cXosVKqtrs%3D
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- ISSN
- 13496336
- 09149244
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- NDL書誌ID
- 9549061
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- NDL
- Crossref
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可