Team:HokkaidoU Japan/Notebook/August10
From 2010.igem.org
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* Added 20 uL of EtBr to 1/2 TBE | * Added 20 uL of EtBr to 1/2 TBE | ||
+ | {|border="1" style="margin-left: 20px;" class="protocol" | ||
+ | !Lane | ||
+ | !DNA | ||
+ | !Length of DNA | ||
+ | |- | ||
+ | | 1 | ||
+ | | pUC1d19/''Hin''f1 | ||
+ | | | ||
+ | |- | ||
+ | | 2 | ||
+ | | 2-24G(sender) | ||
+ | | 847 bp | ||
+ | |- | ||
+ | | 3 | ||
+ | | 1-2M(RBS) | ||
+ | | 61 bp | ||
+ | |- | ||
+ | | 4 | ||
+ | | 1-23L(terminator) | ||
+ | | 178 bp | ||
+ | |- | ||
+ | | 5 | ||
+ | | 3-1E(heat sensor) | ||
+ | | 984 bp | ||
+ | |} | ||
==電気泳動== | ==電気泳動== |
Revision as of 05:49, 20 September 2010
Single Colony Isolation
- Observed if any colonies were made
- Could not see 3-1E
- Number of other colonies on other plates was also very small
- Mistake in protocol is inferred
- Precipitation of cells maybe at fault
- All but 3-1E was moved to new plates
シングルコロニーアイソレーション
コロニーを確認したところ,3-1Eにはコロニーが見られなかった
ほかのプレートもコロニー数が少なかったため,手順に不完全なところがあったのかもしれない
- 実験中に沈殿が見られたため
- コンピテントセルの溶解が不十分だった?
- 混ぜ方が不十分だった?
- 2回目の実験で,若干急いだ感じだったので,吸着などが不十分だった?
3-1E以外を新しい培地に移した
PCR Reaction System
Reaction system was prepared for 3 parts, 245 uL in total
Reagent | Amount |
---|---|
Autoclaved DW | 165 uL |
10x PCR buffer | 25 uL |
2 mM dNTPs | 25 uL |
25 mM MgSO4 | 15 uL |
EX-F primer | 5 uL |
PS-R primer | 5 uL |
KOD plus Neo | 5 uL |
Total | 245 uL |
- 49 uL of reaction solution was added to each of 4 tubes and after DNA template was added
- Length of each template is listed int the table below
Tube | Biobrick | Length |
---|---|---|
1 | 2-24G(sender) | 847 bp |
2 | 1-2M(RBS) | 61 bp |
3 | 1-23L(terminator) | 178 bp |
4 | 3-1E(heat sensor) | 984 bp |
- Template DNA length is calculated by adding prefix and suffix length
- Biobrick Length + Prefix length + Suffix Length
- Because Mini prep of 3-1E failed, it amplified by PCR
PCR反応液の調整
== 今回は4パーツ増幅のためTotal 245 uL作成した.
Autoclaved DW | 165 uL |
10x PCR buffer | 25 uL |
2 mM dNTPs | 25 uL |
25 mM MgSO4 | 15 uL |
EX-F primer | 5 uL |
PS-R primer | 5 uL |
KOD plus Neo | 5 uL |
Total | 245 uL |
- 反応液49 uLを4本のPCRチューブに分注し,Templateを1 uLずつ加えた
- それぞれのPCRチューブとTemplate,lengthは
1 | 2-24G(sender) | 847 bp |
2 | 1-2M(RBS) | 61 bp |
3 | 1-23L(terminator) | 178 bp |
4 | 3-1E(heat sensor) | 984 bp |
- DNA lengthはパーツ長+プライマー(49 bp)
- 3-1EはTransformationがうまくいかなかったため
PCR program
Predenature | 94℃ 2 min |
Denature | 98℃ 10 sec |
Extension | 68℃ 30 sec |
Hold | 4℃ |
- 30 cycles
- KOD potency is 30 sec/kbp, so 30 sec for1cycle
Electrophoresis
- Added 1 uL of 6xSample Buffer to 5 uL of amplified DNA
- Used marker pUC1d19/Hinf1
- Added 20 uL of EtBr to 1/2 TBE
Lane | DNA | Length of DNA |
---|---|---|
1 | pUC1d19/Hinf1 | |
2 | 2-24G(sender) | 847 bp |
3 | 1-2M(RBS) | 61 bp |
4 | 1-23L(terminator) | 178 bp |
5 | 3-1E(heat sensor) | 984 bp |
電気泳動
- 増幅したDNAを5 uLとって6xサンプルバッファー1 uLを加えた
- マーカーはpUC119/Hinf1を使用
- エチブロは20 uL使用