By Hiroshi Nakato, Susumu Izumi, Scott B. Selleck (auth.), Y. Kitagawa, T. Matsuda, S. Iijima (eds.)
Animal mobile know-how is a growing to be self-discipline of telephone biology which goals not just to appreciate buildings, services and behaviors of differentiated animal cells but in addition to envision their skills for use for commercial and scientific reasons. The aim of animal phone know-how comprises accomplishments of clonal enlargement of differentiated cells with helpful skill, optimization in their tradition stipulations, modulation in their skill for creation of medically and pharmaceutically vital proteins, and the applying of animal cells to gene remedy and synthetic organs. This quantity supplies the readers an entire assessment of the current state-of-the-art in Japan. The court cases can be worthwhile for mobilephone biologists, biochemists, molecular biologists, immunologists, biochemical engineers and different disciplines relating to animal phone tradition, operating both in educational environments or in industries of biotechnology and pharmacy.
Read Online or Download Animal Cell Technology: Basic & Applied Aspects: Proceedings of the Tenth Annual Meeting of the Japanese Association for Animal Cell Technology, Nagoya, Japan, November 5–8, 1997 Volume 10 PDF
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Extra resources for Animal Cell Technology: Basic & Applied Aspects: Proceedings of the Tenth Annual Meeting of the Japanese Association for Animal Cell Technology, Nagoya, Japan, November 5–8, 1997 Volume 10
SASAKI, K. KURATA-MIURA, M. HASEGAWA AND T. NISHI Tokyo Research Laboratories, Kyowa Hakko Kogyo Co. Ltd. 3-6-6, Asahi-machi, Machida-shi, Tokyo 194-8533, Japan 1. Introduction The sialyl Lewis oligosaccharide structure and related structures have evoked considerable interest because they serve as ligands for the three known selectins (E-, P-, and L-selectins), which are involved in the recruitment of leukocytes to lymphoid tissues and the sites of inflammation [1, 2]. The compounds which function as selectin antagonists or inhibitors for expression of these adhesion molecules have therapeutic potential as anti-inflammatory drugs.
Biol. Chem. 269, 3054130456. HUMAN CYTOTOXIC T LYMPHOCYTES FOR TUMOR THERAPY Induction on formalin-fixed tumor tissues and expansion on immobilized lectins T. OHNO RIKEN Cell Bank, The Institute of Physical and Chemical Research (RIKEN), Koyadai 3-1-1, Tsukuba Science City, 305, Japan Introduction Cytotoxic T lymphocytes (CTL) exhibit strong killing activity against tumor cells and, therefore, are expected to be employed in adoptive immunotherapy for human tumors. Generation of CTL requires autologous/syngeneic target tumor cells or tumor-derived antigenic peptides presented on antigen-presenting cells.
J. Immunol. 138, 989-995. Pollard, K. S. (1987) Surface antigen preservation by PLP and formalin fixation and the effects of tissue processing. J. Immunol. Methods 96, 145-145. G. (1992) Role of IL-6, IL-2 and IL-4 in the in vitro induction of cytotoxic T cells. J. Immunol. 149, 33163320. H. (1986) Cloned cytotoxic T lymphocytes that recognized an I-A region product in the context of a class I antigen. J. Exp. Med. 163, 972-980. H. (1994) Cytotoxic T-lymphocyte response to autologous human squamous cell cancer of the lung: epitope reconstitution with peptides extracted from HLA-Aw68.