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Team:Tokyo Metropolitan/Notebook/Pattern/2010/10/14
From 2010.igem.org
(Difference between revisions)
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(→7：DNA Digestion) |
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See [https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Pattern/Protocol#Ligation_with_Ligation-convenience_kit_.28NIPPON_GENE.29/ Protocol 10 ] | See [https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Pattern/Protocol#Ligation_with_Ligation-convenience_kit_.28NIPPON_GENE.29/ Protocol 10 ] | ||
| - | === | + | ===4：DNA Digestion=== |
＜Member＞<br /> | ＜Member＞<br /> | ||
nito | nito | ||
| Line 54: | Line 54: | ||
＜Sample, Materials＞<br /> | ＜Sample, Materials＞<br /> | ||
・PCR productions | ・PCR productions | ||
| - | * | + | *plasmid |
| - | + | ||
| - | + | ||
| - | + | ||
| - | + | ||
| - | + | ||
・Digest enzyme | ・Digest enzyme | ||
| - | * | + | *XbaⅠ |
| - | * | + | *SpeⅠ |
＜Protocol＞<br /> | ＜Protocol＞<br /> | ||
See [https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Pattern/Protocol#DNA_Digestion/ Prptpcpl 9 ] | See [https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Pattern/Protocol#DNA_Digestion/ Prptpcpl 9 ] | ||
| - | |||
===1:PCR=== | ===1:PCR=== | ||
Revision as of 10:59, 16 October 2010
Contents |
2010/10/14
1:Electrophoresis
<Member>
nito
<Sample>
- 1-2-7
- 1-2
- 10-2-7
- 9-7
- 4-5
<Protocol>
See Protocol 8
<Result>
2：DNA extraction
＜Member＞
nito
＜Sample＞
- 1-2-7
- 10-2-7
- 9-7
＜Protocol＞
See Protocol 4
3：DNA Ligation
＜Member＞
nito
＜Sample＞
- 4-5
- 1-2-3
- 10-2-3
- 10-2-9
- 7-8-10
(after digestion)
＜Protocol＞
See Protocol 10
4：DNA Digestion
＜Member＞
nito
＜Sample, Materials＞
・PCR productions
- plasmid
・Digest enzyme
- XbaⅠ
- SpeⅠ
＜Protocol＞
See Prptpcpl 9
1:PCR
<Member>
mio
<Sample>
- 1
- 2
- 3
- 4
- 5
- 6
- 7
- 8
<Protocol>
See Protocol 1
7：DNA extraction from gels
＜Member＞
＜Sample＞
- 1+2(8/31)
- 4+5(8/31)
(After electrophoresis)
＜Protocol＞
SeeProtocol 4
7：DNA Digestion
＜Member＞
nito
＜Sample, Materials＞
・PCR productions
- 1
- 2
- 3
- 4
- 6
- 10
・Digest enzyme
- AvrⅡ
- NheⅠ
＜Protocol＞
See Prptpcpl 9
1:PCR
<Member>
mio
<Sample>
- 1
- 2
- 3
- 4
- 5
- 6
- 7
- 8
<Protocol>
See Protocol 1
7：DNA extraction from gels
＜Member＞
＜Sample＞
- 1+2(8/31)
- 4+5(8/31)
(After electrophoresis)
＜Protocol＞
SeeProtocol 4
3:Electrophoresis
<Member>
mio,mizuki
<Sample>
PCR products (9/16)
<Protocol>
See Protocol 8
<Result>
