Presentation is loading. Please wait.

Presentation is loading. Please wait.

實驗課規範 請準時上課 請預讀實驗講義 – 避免因步驟繁雜而做不出實驗 請穿著實驗衣 每天下課時先清點微量分注器 每天由各組排值日生幫忙清理實驗室.

Similar presentations


Presentation on theme: "實驗課規範 請準時上課 請預讀實驗講義 – 避免因步驟繁雜而做不出實驗 請穿著實驗衣 每天下課時先清點微量分注器 每天由各組排值日生幫忙清理實驗室."— Presentation transcript:

1 實驗課規範 請準時上課 請預讀實驗講義 – 避免因步驟繁雜而做不出實驗 請穿著實驗衣 每天下課時先清點微量分注器 每天由各組排值日生幫忙清理實驗室

2 報告 (8/10 統一由班代收齊繳交 ) – 實驗報告 (50%) 目的, 實際操作步驟, 結果 ( 包含判讀 ) 及討論 – 簡答與本週實驗相關問題共十題 (50%) 星期四早上隨堂考 ( 內容為星期一至星期三的上課及實驗 內容, 共 6 題 ) 星期五公佈星期四及星期五的題目 ( 共 4 題 )

3 Molecular cloning 960709

4

5 Streaking E. coli on plate for competent cell production

6

7 In vitro transcription Selectable marker in eukaryotic cells Multiple cloning sites Origen of replication (ORI) Selectable marker in prokaryotic cells Expression cassette

8 pPDX1-FGF10 plasmid DNA

9

10

11

12 1 kb DNA marker

13 Uncut plasmid DNA pcDNA3 pPDX1-FGF10 EcoRI-digested plasmid DNA pcDNA3pPDX1-FGF10

14 CIP and ligation

15 The reaction catalyzed by DNA ligase (DNA replication: lagging strand)

16

17

18

19

20

21

22 p.9

23

24 p.7 65 ℃, 20min 37 ℃, 1hr Gel extraction

25 Gel extraction/band isolation; p.11

26

27 Gel extraction EcoRI Uncut pcDNA3

28 Determination of the amount of isolated DNA Measure DNA concentration by UV spectrophotometer ( 分光光度計 ) OD 260 =1  50  g/ml OD 260/280 =1.8~2.2 3  l plasmid DNA + 297  l ddH2O (100X dilution) OD 260 x 100 (dilution) x 50 1000  g/  l DNA Amount.=

29 Calculating the molar concentration (molarity) of vector and insert DNA Molar concentration (M) = [(  g/  l) ÷ (base pairs X 650 daltons)] X 2 ends Example: *Calculate the molarity of ends if you put 50 ng of a 5 kb vector in a 20  l ligation reaction: 50 ng ÷ 20 μl = 0.0025  g/  l [(0.0025  g/  l) ÷ (5000 X 650)] X 2 = 1.54 X 10 -9 M *Determine the amount of a 1 kb insert should be added to achieve a 1:6 vector:insert ratio: 6 X 1.54 X 10 -9 M = 9.24 X 10 -9 M [( ?  g/  l) ÷ (1000 X 650)] X 2 = 9.24 X 10 -9 M ?= 0.003

30 Actual Vector amount (  g/  l) X x  l = 0.0025  g/  l X 20  l Actual insert amount (  g/  l) X y  l = 0.003  g/  l X 20  l = 0.06  g

31 Ligation V:I = 1:0 or 1:6 ( 助教做 ) EcoRI/CIP-treated vector EcoRI-treated vector (Un-CIP) Vector (50 ng) x ul x ul Insert -- or y ul -- ul 10X buffer A 2 ul 2 ul 10X buffer B 2 ul 2 ul T4 DNA ligase (YEA) 1 ul 1 ul H2O add to 20 ul add to 20 ul  22 o C (at D437), 1 hr  4 o C overnight


Download ppt "實驗課規範 請準時上課 請預讀實驗講義 – 避免因步驟繁雜而做不出實驗 請穿著實驗衣 每天下課時先清點微量分注器 每天由各組排值日生幫忙清理實驗室."

Similar presentations


Ads by Google