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請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/75967
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dc.contributor.author黃曉薇zh_TW
dc.date.accessioned2021-07-01T08:16:51Z-
dc.date.available2021-07-01T08:16:51Z-
dc.date.issued1993
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dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/75967-
dc.description.abstract經鯉魚母系基因轉殖之人類腦下腺腫瘤細胞(Hp-3),與親代細胞(Hpt-1)相比較,已不能在半固態培養基內生長。免疫沈澱及西方點墨分析的結果則顯示,其EGFR之蛋白質量明顯地降低,但GFAP及p53蛋白質則增加。有趣的是,Hp-3細胞對細菌級培養皿的附著情形遠高於Hpt-1細胞,故二種細胞所分泌之細胞外間質,應有極大的差異。
Hpt-1及Hp-3細胞的條件培養液中,含有一活性,可以刺激BL、Hela、NIH 3T3及人類纖維細胞的生長,然而對Hpt-1及Hp-3細胞本身的效果則不顯著。且二細胞條件培養液之刺激生長活性並無明顯差異。以Hela及3T3細胞為主要的分析系統,則發現隨著條件培養液濃度的升高,細胞之增殖亦隨之增加。以0.5 ug/ml anti-bFGF antibody處理條件培養液,並未中和此活性,因而推測此活性應與bFGF無關。
zh_TW
dc.description.provenanceMade available in DSpace on 2021-07-01T08:16:51Z (GMT). No. of bitstreams: 0
Previous issue date: 1993
en
dc.description.tableofcontents壹.中文摘要……………………………………………………I
貳.謝辭……………………………………………………II
參.中文內容
一、緒言……………………………………………………1
二、材料與方法……………………………………………………4
(一)細胞培養……………………………………………………4
(二)質體轉殖……………………………………………………4
(三)DNA雜合反應……………………………………………………4
(四)RNA雜合反應……………………………………………………5
(五)不同條件下細胞的生長……………………………………………………5
(六)致癌能力分析……………………………………………………5
(七)西方點墨分析……………………………………………………5
(八)細胞免疫染色……………………………………………………6
(九)免疫沉澱……………………………………………………6
(十)條件培養液的製備……………………………………………………6
(十一)濃縮條件培養液……………………………………………………6
(十二)刺激細胞生長活性之分析……………………………………………………7
三、結果……………………………………………………8
(一)母系基因之轉殖……………………………………………………8
(二)Hpt-1及Hp-3細胞的生長模式……………………………………………………8
(三)細胞在細菌級培養皿上生長的比較……………………………………………………9
(四)Hpt-1及Hp-3細胞基因表現的不同……………………………………………………9
(五)存於Hpt-1及Hp-3條件培養液內之促進生長活性……………………………………………………9
(六)條件培養液內之生長因數並非bFGF……………………………………………………10
四、討論……………………………………………………11
肆.英文內容……………………………………………………13
dc.language.isozh-TW
dc.title人類腦下腺腫瘤細胞株經鯉魚母系基因轉型後其生長及分化之研究zh_TW
dc.titleGrowth and Differentiation of Carp Maternal Gene Transformed Human Pituitary Gland Tumor Cellsen
dc.date.schoolyear81-2
dc.description.degree碩士
dc.relation.page60
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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