Team:HokkaidoU Japan/Notebook/August11

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Latest revision as of 07:27, 27 October 2010

August 10

Notebook

August 12

LB Culture

For every 2 mL of LB added 2 uL of antibiotics
Transfered a colony to LB
One colony didn't grow well so we isolated another one
Prepared more tubes for mini preps int he future

glycerol Stock

Added 1 mL of 80% Glycerol to screw cap tube
Added 1 mL of cell and broth solution to Glycerol after 2h of incubation
Sored at -80℃

Ligation

DNA Preparation for Ligation

Used 49 uL of yesterdays PCR product
Removed primers via Microcon YM-10
- Added 450 uL of TE to make final volume of 500 uL
- Centrifuged at 10000 G for more than an hour till all 4 samples volume was less then 45 uL
Measured the final amount of samples and added TE till all were 45 uL
- Used 500 uL tubes

Ligation System

From PCR products we only used No.3 （1-23L（terminator）178 bp made on previous day

Tube No.	１	２	３	４
PCR products	1 uL	1 uL	1 uL	1 uL
10x H Buffer	-	1 uL	1 uL	1 uL
DW	9 uL	7.5 uL	7.0 uL	7.5 uL
Xba1	-	0.5 uL	0.5 uL	-
Pst1	-	-	0.5 uL	0.5 uL
Restriction Enzyme Digestion	4C	at 37C for 60 min
Restriction enzyme Inactivation	at 60C for 15 min
ligation solution	10 uL	10 uL	10 uL	10 uL
Ligation	at 16C for 30 min
6x SB	4 uL	4 uL	4 uL	4 uL

→1% Agarose Gel Electrophoresis in 1/2 TBE + EtOH

Electrophoresis

Performed electrophoresis for every digested sample, 1 through 4
Used marker pUC119/Hinf
DNA solution was too　diluted and no bands were visible

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 {{Template:HokkaidoU_Japan}}<div class="linkbar"><div class="prev">[[Team:HokkaidoU_Japan/Notebook/August10|August 10]]</div>[[Team:HokkaidoU_Japan/Notebook|Notebook]]<div class="next">[[Team:HokkaidoU_Japan/Notebook/August12|August 12]]</div></div>
-==LB培養==
+==LB Culture==
-* 2 mLのLBに抗生物質を2 uLずつ加えた
+* For every  2 mL of LB added 2 uL of antibiotics
-* 白金耳でコロニーをとり，LBに移した
+* Transfered a colony to LB
-* １本以外は生育が悪かったため，再び作り直した
+* One colony didn't grow well so we isolated another one
-* 同時に，翌日のmini prepのために2 mLずつ作った
+* Prepared more tubes for mini preps int he future
-==グリセロールストック作成==
+==glycerol Stock==
-* 80% Glycerol 1 mLをスクリューキャップのチューブにとった
+* Added 1 mL of 80% Glycerol to screw cap tube
-* やや濁った（約2時間培養）LB液体培地を1 mLとり，加えた
+* Added 1 mL of cell and broth solution to Glycerol after 2h of incubation
-* -80℃に保存した
+* Sored at -80℃
 ==Ligation==
-===ligation用DNAの調製===
+===DNA Preparation for Ligation===
-* 前日にPCRした50 uLのうち電気泳動しなかった49 uLを使用した
+* Used 49 uL of yesterdays PCR product
-* 制限酵素処理するまえにプライマーを除去するため，ろ過を行った
+* Removed primers via Microcon YM-10
-** 分子量10000 Da以下を通すフィルタ（緑チューブ）を使用
+** Added 450 uL of TE to make final volume of 500 uL
-** 500 uLにするため450 uLのTEを加えた
+** Centrifuged at 10000 G for more than an hour till all 4 samples volume was less then 45 uL
-** ４サンプルすべてが45 uL以下になるまで１時間以上，10000Gで遠心した
+* Measured the final amount of samples and added TE till all were 45 uL
-* 遠心したサンプルの容量を量り，（元の）45 uLになるようにTEでメスアップした
+** Used 500 uL tubes
-** 後でLigation反応をするウォーターバスが500 uLチューブ用なので，これを使用した
+===Ligation System===
+From PCR products we only used No.3 （[[Team:HokkaidoU_Japan/Parts#BioBricks|1-23L]]（terminator）178 bp made on previous day
-===ligation反応系===
-PCR productsは前日に作成した３番（1-23L（terminator）178 bp）を１つだけ使用した
 {| style="text-align:center;" class="protocol"
 |-
-|style="border-bottom:1px solid #000; border-right:1px solid #000;"|
+|style="border-bottom:1px solid #996; border-right:1px solid #996;"|'''Tube No.'''
-|style="border-bottom:1px solid #000;"|  １
+|style="border-bottom:1px solid #996;"|  １
-|style="border-bottom:1px solid #000;"|  ２
+|style="border-bottom:1px solid #996;"|  ２
-|style="border-bottom:1px solid #000;"|  ３
+|style="border-bottom:1px solid #996;"|  ３
-|style="border-bottom:1px solid #000;"|  ４
+|style="border-bottom:1px solid #996;"|  ４
 |-
-|style="border-right:1px solid #000;"| PCR products
+|style="border-right:1px solid #996;"| PCR products
 | 1 uL
 | 1 uL
@@ Line 38: / Line 39: @@
 | 1 uL
 |-
-|style="border-right:1px solid #000;"| 10x H Buffer
+|style="border-right:1px solid #996;"| 10x H Buffer
 | -
 | 1 uL
@@ Line 44: / Line 45: @@
 | 1 uL
 |-
-|style="border-right:1px solid #000;"| DW
+|style="border-right:1px solid #996;"| DW
 | 9 uL
 | 7.5 uL
@@ Line 50: / Line 51: @@
 | 7.5 uL
 |-
-|style="border-right:1px solid #000;"| Xba1
+|style="border-right:1px solid #996;"| Xba1
 | -
 | 0.5 uL
@@ Line 56: / Line 57: @@
 | -
 |-
-|style="border-right:1px solid #000; border-bottom:1px solid #000;"| Pst1
+|style="border-right:1px solid #996; border-bottom:1px solid #996;"| Pst1
-|style="border-bottom:1px solid #000;"| -
+|style="border-bottom:1px solid #996;"| -
-|style="border-bottom:1px solid #000;"| -
+|style="border-bottom:1px solid #996;"| -
-|style="border-bottom:1px solid #000;"| 0.5 uL
+|style="border-bottom:1px solid #996;"| 0.5 uL
-|style="border-bottom:1px solid #000;"| 0.5 uL
+|style="border-bottom:1px solid #996;"| 0.5 uL
 |-
-|style="border-right:1px solid #000;"| 制限酵素処理
+|style="border-right:1px solid #996;"| Restriction Enzyme Digestion
-| 4℃
+| 4C
-|colspan="3" style="background-color:#DDD7B0;"| @37℃ 60 min
+|colspan="3" style="background-color:#DDD7B0;"| at 37C for 60 min
 |-
-|style="border-right:1px solid #000;"| 制限酵素不活化
+|style="border-right:1px solid #996;"| Restriction enzyme Inactivation
-| colspan="4" style="background-color:#DDD7B0;"| @60℃ 15 min
+| colspan="4" style="background-color:#DDD7B0;"| at 60C for 15 min
 |-
-|style="border-right:1px solid #000;"| ligation solution
+|style="border-right:1px solid #996;"| ligation solution
 | 10 uL
 | 10 uL
@@ Line 75: / Line 76: @@
 | 10 uL
 |-
-|style="border-right:1px solid #000;"| Ligation反応
+|style="border-right:1px solid #996;"| Ligation
-| colspan="4" style="background-color:#DDD7B0;"|@16℃ 30 min
+| colspan="4" style="background-color:#DDD7B0;"|at 16C for 30 min
 |-
-|style="border-right:1px solid #000;"| 6x SB
+|style="border-right:1px solid #996;"| 6x SB
 | 4 uL
 | 4 uL
@@ Line 86: / Line 87: @@
 |}
-→1% Agarose Gel Electrophoresis in 1/2 TBE
+→1% Agarose Gel Electrophoresis in 1/2 TBE + EtOH
-==電気泳動==
-* 制限酵素処理したサンプル１～４を電気泳動した
+==Electrophoresis==
-* マーカーはpUC119/''Hin''f
+* Performed electrophoresis for every digested sample, 1 through 4
-* DNA solutionが薄すぎたため，バンドが見えなかった
+* Used marker [https://2010.igem.org/Image:HokkaidoU_Pictures_DNA_Marker.png pUC119/''Hin''f]
+* DNA solution was too　diluted and no bands were visible