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Revision as of 06:33, 28 September 2010 (view source) Mizuki (Talk | contribs) (→5：Electrophoresis) ← Older edit		Revision as of 10:33, 19 October 2010 (view source) Mizuki (Talk | contribs) (→1：Electrophoresis) Newer edit →
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	＜Sample＞<br />		＜Sample＞<br />
	PCR products.		PCR products.
-	*1 (8/25)	+	*[https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Pattern/Protocol#Sample_Number/1] (8/25)
-	*3 (8/26)	+	*[https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Pattern/Protocol#Sample_Number/3] (8/26)
-	*4 (8/26)	+	*[https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Pattern/Protocol#Sample_Number/4] (8/26)
-	*5 (8/26)	+	*[https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Pattern/Protocol#Sample_Number/5] (8/26)
-	*7(8/30)	+	*[https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Pattern/Protocol#Sample_Number/7] (8/30)
-	*8(8/30)	+	*[https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Pattern/Protocol#Sample_Number/8] (8/30)

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Revision as of 10:33, 19 October 2010

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Acknowledgment

Contents 1 2010/08/31 1.1 1：Electrophoresis 1.2 2：PCR 1.3 3：DNA Digestion 1.4 4：Electrophoresis 1.5 5：Electrophoresis 1.6 6：DNA extraction 1.7 7：DNA extraction from gels 1.8 8：DNA Ligation 1.9 9：Electrophoresis

2010/08/31

1：Electrophoresis

＜Member＞
Hitomi

＜Sample＞
PCR products.

• [1] (8/25)
• [2] (8/26)
• [3] (8/26)
• [4] (8/26)
• [5] (8/30)
• [6] (8/30)

＜Protocol＞
SeeProtocol 8

＜Result＞

2：PCR

＜Member＞
nito

＜Sample＞
・E-coli (having BBa_I13521 plasmid)

・E-coli (having BBa_K208017 plasmid)

・E-coli (having BBa_I732901 plasmid)

＜Protocol＞
See Protocol 2

・Tube (temperature in annealing)

1. Promoter~signal (72.0℃)
2. cyaA (71.5)
3. mRFP~Terminator (69.0)
4. Promoter (70.0)
5. RBS~signal (70.0)
6. lacZ (63.5)
7. Terminator (67.5)
8. CRP (72.5)

All tubes ×3. Total 24 tubes.

3：DNA Digestion

＜Member＞
Mariko, Hitomi

＜Sample, Materials＞
・PCR productions

• 1L(8/25) 8μl
• 2L(8/26) 8μl
• 4H(8/26) 16μl
• 5H(8/26) 16μl

・Digest enzyme

• AvrⅡ
• NheⅠ
• SpeⅠ

＜Protocol＞
See Protocol 9

4：Electrophoresis

＜Member＞
nito, Hitomi

＜Sample＞
・PCR products

＜Protocol＞
SeeProtocol 8

＜Result＞

5：Electrophoresis

＜Member＞
Mariko, nito

＜Sample＞

• 1+2(8/31)
• 4+5(8/31)

(after digestion)

＜Protocol＞
SeeProtocol 8

And cut off gels included DNA.

6：DNA extraction

＜Member＞
nito

＜Sample＞
・PCR productions (8/31)

＜Protocol＞
SeeProtocol 4

7：DNA extraction from gels

＜Member＞
nito

＜Sample＞

• 1+2(8/31)
• 4+5(8/31)

(After electrophoresis)

＜Protocol＞
SeeProtocol 4

8：DNA Ligation

＜Member＞
nito

＜Sample＞

• 1L(8/25)
• 2L(8/26)
• 4H(8/26)
• 5H(8/26)

(after digestion)

＜Protocol＞
See Protocol 3

We ligated 1 and 2, 4 and 5.

9：Electrophoresis

＜Member＞
nito

＜Sample＞

• 1+2(8/31)
• 4+5(8/31)

(After ligation)

＜Protocol＞
SeeProtocol 8

＜Result＞