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dc.contributor.author徐肇謙zh_TW
dc.date.accessioned2021-07-01T08:14:51Z-
dc.date.available2021-07-01T08:14:51Z-
dc.date.issued1989
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dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/75713-
dc.description.abstract本實驗是以LF,TO2和BGK?材料,來探討熱和硫酸鎘對細胞的交互影響,進而探討應用魚類細胞來評估水質的可行性。
硫酸鎘對LF,TO2及BGK的96h LC50分別?50,40,80μM,經37℃前處理1小時後,LF 96h LC50上升?80μM,而TO2和BGK則大於100μM:經41℃前處理30分鍾後96h LC50分別上升?90,70,及100μM。
由SDS-PAGE知經硫酸鎘與熱處理後,LF會?生hsp87,hsp80,hsp70,hsp32,hsp27,hsp23及hsp21;TO2則?生hsp87,hsp70,hsp27及hsp25;BGK則產生hsp87,hsp70,hsp25及hsp23四種蛋白質。
由雙向電泳實驗結果知,經100μM硫酸鎘和熱處理後,LF有四種熱休克蛋白質?生,TO2則有10種,BGK計有20種熱休克蛋白質?生。
由cytoplasmic dot hybridization實驗結果指出:LF,TO2及BGK三種細胞都有Metallothionein基因存在,但100μM硫酸鎘在24小時內卻不會誘發 Metallothionein mRNA 的合成。由PAGE解析卻發現,LF在72小時有 Metallothionein-like合成,TO2和BGK則在43小時就?生。
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dc.description.tableofcontents目錄
壹.前言………………………01-08
貳.材料與方法………………09-22
一.材料……………………09
1.細胞株與細胞培養……………………09
2.質體……………………09
3.硫酸鎘的制備…………………………10
4.放射性物質的制備………………………10
5.EDTA-磷酸監緩衝液的制備…………10
6.胰蛋白?溶液…………………11
7.電泳貯藏液的制備…………………11
二.方法…………………………14
1.鎘和熱對細胞的影響…………14
2.蛋白質電泳分析……………………15
(1)雙向電泳……………………15
(2)SDS-PAGE…………………16
(3)PAGE………………………19
3.放射性自動顯影術…………………19
4.DNA Dot Hybridization………………19
5.RNA Dot Hybridiazaton………………20
參.結果………………………23-29
一.硫酸鎘的毒性……………………………23
二.溫度處理對細胞存活的影響……………23
三.不同溫度處理後硫酸鎘對細胞株的毒性效應…………24
四.細胞株蛋白質的SDS-PAGE與雙向電泳解析……25
五.Cytoplasmic Dot Hybridization…………………29
六.細胞株Metallothionein 的PAGE解析…………29
肆.討論…………………………………………30-35
伍.參考文獻
陸.圖表
dc.language.isozh-TW
dc.title溫度與鎘對魚類細胞株影響之研究zh_TW
dc.titleEffects of Temperature and Cadmium on Fish cell Linesen
dc.date.schoolyear77-2
dc.description.degree碩士
dc.relation.page82
dc.rights.note未授權
dc.contributor.author-dept生命科學院zh_TW
dc.contributor.author-dept漁業科學研究所zh_TW
顯示於系所單位:漁業科學研究所

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