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  1. NTU Theses and Dissertations Repository
  2. 生命科學院
  3. 動物學研究所
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/75522
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dc.contributor.authorShiu-Nan Chenen
dc.contributor.author陳重仁zh_TW
dc.date.accessioned2021-07-01T08:13:39Z-
dc.date.available2021-07-01T08:13:39Z-
dc.date.issued1985
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3 Chen, J.H., S.N. Chen, H.H. Shih and G.H. Kou (1983 b). Proceeding of ROC-Japan Cooperative Science Seminar on Fish Diseases 93.
4. Freshy, R.I. (1972). Lancet Sept. 2,488.
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dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/75522-
dc.description.abstractThe first In Vitro successfully established human ovarian cancer cell line in Taiwan area, designated OC-3/VGH was made from a patient with serious papillary adenocarcinoma of the ovary, using Dulbecco’s Modified Eagle’s Medium (DMEM) supplemented with 10-20% fetal calf serum. The cells were derived from patient’s tumor tissue and grew as a monolayer of epithloid cells in culture. The cells have a doubling time of 48 hours determined by using a haemacytometer. Giemsa banding of mataphase chromosomes had revealed that the distribution of chromosome number of OC-3/VGH varied widely from 38 to 68 with a model number of 62. The cells have been subcultured 97 passages since its initiation in June, 1983, and maintainted in active culture in Laboratory of Tumor Biology at Veterans General Hospital, Taipei. It is believed that the establishment of this cell line will provide an useful in vitro model for Gynecological neoplastims studies.en
dc.description.provenanceMade available in DSpace on 2021-07-01T08:13:39Z (GMT). No. of bitstreams: 0
Previous issue date: 1985
en
dc.description.tableofcontentsAbstract…………2
Introduction……3
Materials & Methods………6-12
I. Materials……………………6-8
1. Tumor Tissue…………………6
2. Culture Media………………6
3. Hank’s Balanced Salt Solution (HBSS)……………6
4. Phosphate Buffer Solution…………………7
5. Trypsin /(EDTA) Solution…………………7
6. Giemsa Banding Solution…………………8
II. Methods…………………………8-12
1. Primary Culture……………………8
2. Subculture…………………………8
3. Growth Kinetics……………………9
4. Cell Storage in Frozen State……9
5. Reconstitution of Frozen Cells………10
6. Phase Contrast Microscopy…………10
7. Scanning Electron Microscopy………10
8. Tumorigenecity……………………11
9. Chromosome Study………………11
10. Bacteria Test………………12
11. Mycoplasma Test……………12
Results…………………13
Discussion…………………16
Figures………………20
Reference……………30
dc.language.isozh-TW
dc.title人類卵巢癌瘤細胞株之試管培養及其特性之研究zh_TW
dc.date.schoolyear73-2
dc.description.degree碩士
dc.relation.page31
dc.rights.note未授權
dc.contributor.author-dept生命科學院zh_TW
dc.contributor.author-dept動物學研究所zh_TW
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