Abstract
The project aims to establish basic technologies for the mass culture of cells which will enable a large, stable supply of fine chemical products whose industrial production the conventional technique of synthesis has failed to realize. In the 1st phase, cell stains were selected, a serumless medium was developed, basic culturing conditions were established, and substances production rates were improved, and the 2nd phase stands succeeding these 1st phase achievements. Toward the ultimate goal of establishing basic technologies for serumless high-density cultures for industrial use and technologies for isolating and refining useful substances, a small-scale optimum culture technique and a serumless culture technique are developed. Serumless cultures are developed for strains of man's lymphoid cells, cells deriving from bone marrow, epithelial cells, and hybridomas of man and mouse, all these sampled during the 1st phase endeavors. Success is attained in growing each cell strain on a scale of 1-10L to increase to 10{sup 7} cells/ml or more in population density. It is found that each cell strain produces useful substances, such as man's monoclonal antibodies and elements involved in the multiplication or differentiation of new cells. (NEDO)
Citation Formats
None.
Research and development of basic technologies for next-generation industries. Evaluation of 2nd phase research and development of technologies of mass culture of cells; Jisedai sangyo kiban gijutsu kenkyu kaihatsu saibo tairyo baiyo gijutsu. Dainiki kenkyu kaihatsu hyoka.
Japan: N. p.,
1987.
Web.
None.
Research and development of basic technologies for next-generation industries. Evaluation of 2nd phase research and development of technologies of mass culture of cells; Jisedai sangyo kiban gijutsu kenkyu kaihatsu saibo tairyo baiyo gijutsu. Dainiki kenkyu kaihatsu hyoka.
Japan.
None.
1987.
"Research and development of basic technologies for next-generation industries. Evaluation of 2nd phase research and development of technologies of mass culture of cells; Jisedai sangyo kiban gijutsu kenkyu kaihatsu saibo tairyo baiyo gijutsu. Dainiki kenkyu kaihatsu hyoka."
Japan.
@misc{etde_20090341,
title = {Research and development of basic technologies for next-generation industries. Evaluation of 2nd phase research and development of technologies of mass culture of cells; Jisedai sangyo kiban gijutsu kenkyu kaihatsu saibo tairyo baiyo gijutsu. Dainiki kenkyu kaihatsu hyoka}
author = {None}
abstractNote = {The project aims to establish basic technologies for the mass culture of cells which will enable a large, stable supply of fine chemical products whose industrial production the conventional technique of synthesis has failed to realize. In the 1st phase, cell stains were selected, a serumless medium was developed, basic culturing conditions were established, and substances production rates were improved, and the 2nd phase stands succeeding these 1st phase achievements. Toward the ultimate goal of establishing basic technologies for serumless high-density cultures for industrial use and technologies for isolating and refining useful substances, a small-scale optimum culture technique and a serumless culture technique are developed. Serumless cultures are developed for strains of man's lymphoid cells, cells deriving from bone marrow, epithelial cells, and hybridomas of man and mouse, all these sampled during the 1st phase endeavors. Success is attained in growing each cell strain on a scale of 1-10L to increase to 10{sup 7} cells/ml or more in population density. It is found that each cell strain produces useful substances, such as man's monoclonal antibodies and elements involved in the multiplication or differentiation of new cells. (NEDO)}
place = {Japan}
year = {1987}
month = {Mar}
}
title = {Research and development of basic technologies for next-generation industries. Evaluation of 2nd phase research and development of technologies of mass culture of cells; Jisedai sangyo kiban gijutsu kenkyu kaihatsu saibo tairyo baiyo gijutsu. Dainiki kenkyu kaihatsu hyoka}
author = {None}
abstractNote = {The project aims to establish basic technologies for the mass culture of cells which will enable a large, stable supply of fine chemical products whose industrial production the conventional technique of synthesis has failed to realize. In the 1st phase, cell stains were selected, a serumless medium was developed, basic culturing conditions were established, and substances production rates were improved, and the 2nd phase stands succeeding these 1st phase achievements. Toward the ultimate goal of establishing basic technologies for serumless high-density cultures for industrial use and technologies for isolating and refining useful substances, a small-scale optimum culture technique and a serumless culture technique are developed. Serumless cultures are developed for strains of man's lymphoid cells, cells deriving from bone marrow, epithelial cells, and hybridomas of man and mouse, all these sampled during the 1st phase endeavors. Success is attained in growing each cell strain on a scale of 1-10L to increase to 10{sup 7} cells/ml or more in population density. It is found that each cell strain produces useful substances, such as man's monoclonal antibodies and elements involved in the multiplication or differentiation of new cells. (NEDO)}
place = {Japan}
year = {1987}
month = {Mar}
}