Development of the cell analysis chip (II)

Tatsuya Munaka; Masaki Kanai; Hirohisa Abe; Hiroaki Nakanishi; Takashi Sakamoto; Akio Kobori; Tetsuji Yamaoka; Shuichi Shoji; Akira Murakami

Development of the cell analysis chip (II)

Tatsuya Munaka^*, Masaki Kanai, Hirohisa Abe, Hiroaki Nakanishi, Takashi Sakamoto, Akio Kobori, Tetsuji Yamaoka, Shuichi Shoji, Akira Murakami

^*Corresponding author for this work

School of Fundamental Science and Engineering

Research output: Contribution to conference › Paper › peer-review

Abstract

In recent years, cell analysis has attracted increased attention in bioanalytical and biotechnological applications. On the other hand, microchip techniques, which are called micro total analysis systems (μTAS), have been developed especially in chemical and biochemical analysis fields. We took advantage of a feature of μ TAS and developed a system that can detect a small amount of the protein released by a cell without bound/free (B/F) separation protocol and with high sensitivity. In this report, we describe the continuous monitoring of immunoglobulin G (lgG) production of hybridoma cells stimulated by the serum.

Original language	English
Number of pages	1
Publication status	Published - 2005 Dec 1
Event	54th SPSJ Annual Meeting 2005 - Yokohama, Japan Duration: 2005 May 25 → 2005 May 27

Conference

Conference	54th SPSJ Annual Meeting 2005
Country/Territory	Japan
City	Yokohama
Period	05/5/25 → 05/5/27

Keywords

Cell analysis
Micro total analysis systems
Time-resolved luminescence anisotropy analysis

ASJC Scopus subject areas

Engineering(all)

Cite this

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title = "Development of the cell analysis chip (II)",

abstract = "In recent years, cell analysis has attracted increased attention in bioanalytical and biotechnological applications. On the other hand, microchip techniques, which are called micro total analysis systems (μTAS), have been developed especially in chemical and biochemical analysis fields. We took advantage of a feature of μ TAS and developed a system that can detect a small amount of the protein released by a cell without bound/free (B/F) separation protocol and with high sensitivity. In this report, we describe the continuous monitoring of immunoglobulin G (lgG) production of hybridoma cells stimulated by the serum.",

keywords = "Cell analysis, Micro total analysis systems, Time-resolved luminescence anisotropy analysis",

author = "Tatsuya Munaka and Masaki Kanai and Hirohisa Abe and Hiroaki Nakanishi and Takashi Sakamoto and Akio Kobori and Tetsuji Yamaoka and Shuichi Shoji and Akira Murakami",

year = "2005",

month = dec,

day = "1",

language = "English",

note = "54th SPSJ Annual Meeting 2005 ; Conference date: 25-05-2005 Through 27-05-2005",

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TY - CONF

T1 - Development of the cell analysis chip (II)

AU - Munaka, Tatsuya

AU - Kanai, Masaki

AU - Abe, Hirohisa

AU - Nakanishi, Hiroaki

AU - Sakamoto, Takashi

AU - Kobori, Akio

AU - Yamaoka, Tetsuji

AU - Shoji, Shuichi

AU - Murakami, Akira

PY - 2005/12/1

Y1 - 2005/12/1

N2 - In recent years, cell analysis has attracted increased attention in bioanalytical and biotechnological applications. On the other hand, microchip techniques, which are called micro total analysis systems (μTAS), have been developed especially in chemical and biochemical analysis fields. We took advantage of a feature of μ TAS and developed a system that can detect a small amount of the protein released by a cell without bound/free (B/F) separation protocol and with high sensitivity. In this report, we describe the continuous monitoring of immunoglobulin G (lgG) production of hybridoma cells stimulated by the serum.

AB - In recent years, cell analysis has attracted increased attention in bioanalytical and biotechnological applications. On the other hand, microchip techniques, which are called micro total analysis systems (μTAS), have been developed especially in chemical and biochemical analysis fields. We took advantage of a feature of μ TAS and developed a system that can detect a small amount of the protein released by a cell without bound/free (B/F) separation protocol and with high sensitivity. In this report, we describe the continuous monitoring of immunoglobulin G (lgG) production of hybridoma cells stimulated by the serum.

KW - Cell analysis

KW - Micro total analysis systems

KW - Time-resolved luminescence anisotropy analysis

UR - http://www.scopus.com/inward/record.url?scp=33645647573&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=33645647573&partnerID=8YFLogxK

M3 - Paper

AN - SCOPUS:33645647573

T2 - 54th SPSJ Annual Meeting 2005

Y2 - 25 May 2005 through 27 May 2005

ER -

Development of the cell analysis chip (II)

Abstract

Conference

Keywords

ASJC Scopus subject areas

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