Simultaneous Imaging of Multiple Fluorescent Probes in Bio-Cells.
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- MATSUOKA Hideaki
- Department of Biotechnology and Life Science, Tokyo University of Agriculture and Technology
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- KOSAI Yuri
- Department of Biotechnology and Life Science, Tokyo University of Agriculture and Technology
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- SAITOI Mikako
- Department of Biotechnology and Life Science, Tokyo University of Agriculture and Technology
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- TAKEYAMA Norihide
- Genesia Corporation
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- SUTO Hiroshi
- National Astronomical Observatory of Japan
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In order to obtain the full spectrum from 400 to 800 nm of each pixcel of a microscopic image, a unique spectro-imaging system was developed using an image slicer. The image slicer is composed of 100 photo fibers which are arranged in a matrix of 10 × 10 at the entrance and 100 × 1 at the exit. A line of this 100 signals is passed through a glism and projected onto a CCD. This system was applied to the fluorescent imaging of bio-cells. One of the demonstrative examples was simultaneous measurements of the Ca2+ concentration and the pH using of respective fluorescent probes. An electric signal was applied to BY-2 protoplasts and the fluorescent spectrum from 500 nm to 800 nm was measured every 5 s. The spectrum of the BY-2 protoplasts changed in response to the electric signal and the Ca2+ concentration, and the pH changes could be monitored. The wavelength resolution was satisfactory, but the space resolution was still rough in comparison with the usual microscopic systems. Notwithstanding these conditions, we could obtain discrete data from more than several tens of sites in a single-cell or a chain of several cells.
収録刊行物
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- Analytical Sciences
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Analytical Sciences 18 (12), 1321-1324, 2002
社団法人 日本分析化学会
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詳細情報 詳細情報について
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- CRID
- 1390282679234722432
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- NII論文ID
- 130004440513
- 10011309696
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- NII書誌ID
- AA10500785
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- COI
- 1:CAS:528:DC%2BD38XpslWlt70%3D
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- ISSN
- 13482246
- 09106340
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- NDL書誌ID
- 6393285
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- PubMed
- 12502082
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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
- PubMed
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可