Team:HokkaidoU Japan/Notebook/August18

From 2010.igem.org

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(→RBS 再リベンジ)
 
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|style="border-top:1px solid #996"|'''20 uL'''
|style="border-top:1px solid #996"|'''20 uL'''
|}
|}
-
→Incubated at 37C for 60 min
+
->Incubated at 37C for 60 min
* Added 4 uL of 6x Sample Buffer making it total of 12 uL per lane and electrophoresed  
* Added 4 uL of 6x Sample Buffer making it total of 12 uL per lane and electrophoresed  
-
→Extracted for gel <br>
+
->Extracted for gel <br>
-
→Electrophoresed 10 uL of Extracted DNA
+
->Electrophoresed 10 uL of Extracted DNA
* Used [https://2010.igem.org/Image:HokkaidoU_Pictures_DNA_Marker.png TSUDA Marker 1]  
* Used [https://2010.igem.org/Image:HokkaidoU_Pictures_DNA_Marker.png TSUDA Marker 1]  
Line 39: Line 39:
=Ligation=
=Ligation=
===Preparation of DNA Solution for Ligation===
===Preparation of DNA Solution for Ligation===
-
{|style="text-align:center;" class="protocol"
+
{|border="1px" style="text-align:center;" class="protocol"
|-
|-
!Part
!Part
-
!By comparison to[https://2010.igem.org/Image:HokkaidoU_Pictures_DNA_Marker.png Lambda/''Hin''d III] (ng/10 uL)
+
!By comparison to[https://2010.igem.org/Image:HokkaidoU_Pictures_DNA_Marker.png λ/''Hin''d III]<br>(ng/10 uL)
!ng/uL
!ng/uL
!ratio
!ratio
-
!size (bp)
+
!size(bp)
-
!(ng) required
+
!required(ng)
-
!(uL) used
+
!used(uL)
|-
|-
|Vector
|Vector
Line 65: Line 65:
|0.3 uL
|0.3 uL
|-
|-
-
|double terminator
+
|terminator
|5 ng/10 uL
|5 ng/10 uL
|0.5 ng/uL
|0.5 ng/uL
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|}
|}
-
===Ligation and Transformation===
+
===Ligation and [[Team:HokkaidoU_Japan/Protocols|Transformation]]===
{|style="text-align:center;" class="protocol"
{|style="text-align:center;" class="protocol"
!Reagent
!Reagent
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* Incubated at 37C for 120 min
* Incubated at 37C for 120 min
* Spread onto the LBC plate
* Spread onto the LBC plate
-
* ncubated at 37C for 15~20 hrs
+
* Incubated at 37C for 20 hrs
=RBS Retry=
=RBS Retry=
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|style="border-top:1px solid #996"|'''20 uL'''
|style="border-top:1px solid #996"|'''20 uL'''
|}
|}
-
→37℃，60 min
+
->Incubated at 37C for 60 min
-
==エタ沈==
+
==[[Team:HokkaidoU_Japan/Protocols|Ethanol Precipication]]==
-
* 2 uLの3 M 酢酸ナトリウムを加えた
+
* Added 2 uL of sodium acetate(3 M)
-
* 44 uLのエタノールを加えた
+
* Added 44 uL of Ethanol
-
* 液体窒素の中で凍らせた（'''1.5 mLのチューブに移す'''）
+
* Transfered to 1.5 mL tube and frozen with liquid nitrogen
-
* 溶かしてから15,996 rpm @4℃で５分間遠心した
+
* Melted and centrifuged at 15000 rpm, 4C for 5 min
-
* 上清をほかのチューブに移した（一応これも遠心し，上清を捨て，同じ操作をした）
+
* Transfered supernatant to another tube
-
* 100 uLの70%エタノールで壁をリンスし，15,996 rpm @4℃で５分間遠心した
+
** Driven by precaution centrifuged the supernatant and discarded it's supernatant
-
* 上清を捨て，真空デシケータで乾燥させた
+
* Rinsed the tube walls with 100 uL of 70% Ethanol and centrifuged at 15000 rpm, 4C for 5 min
-
* TE 5 uLで溶かした
+
* Discarded the supertenant and dried via vacuum desiccator
 +
* Melted in 5 uL of TE
-
==電気泳動==
+
==Electrophoresis==
-
[[Image:HokkaidoU Japan 20100818b.JPG‎|200px|right|thumb|]]
+
[[Image:HokkaidoU Japan 20100818b.JPG‎|200px|right|thumb| Electrophoresis after Ethanol presipication]]
-
* TEで溶かしたDNA Solution 1 uLに6x SB 1 uLを加えた
+
* Added 1 uL of 6x SB to DNA Solution of 1 uL
-
* 最初にとった上清も同じ操作をした
+
* Did the same to supernatant　retreaved for precaution
{| class="protocol"
{| class="protocol"
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|-
|-
|2
|2
-
|TSUDA Marker 1
+
|[https://2010.igem.org/Image:HokkaidoU_Pictures_DNA_Marker.png TSUDA Marker 1]
|-
|-
|3
|3
-
|上清
+
|supernatant
|-
|-
|4
|4
|DNA solution
|DNA solution
|}
|}
-
* DNA solutionにしっかり回収されていた
+
* DNA solution band is visible
 +
** Looks OK

Latest revision as of 13:28, 27 October 2010

Notebook

RBS digestion: Revenge

HokkaidoU Japan 20100818a.JPG
Reagent Amount
1-2M 10 uL
DW 4 uL
10x M Buffer 2 uL
BSA 2 uL
Xba I 1 uL
Pst I 1 uL
Total 20 uL

->Incubated at 37C for 60 min

  • Added 4 uL of 6x Sample Buffer making it total of 12 uL per lane and electrophoresed

->Extracted for gel
->Electrophoresed 10 uL of Extracted DNA

Failure

  • After better inspection of Kit specs it came to lite that retreavel rate for 50 bp and less is 26%
    • RBS is just quite small when cut

Ligation

Preparation of DNA Solution for Ligation

Part By comparison toλ/Hind III
(ng/10 uL) 		ng/uL ratio size(bp) required(ng) used(uL)
Vector 50 ng/10 uL 5 ng/uL 1 2996 bp 10 ng 2 uL
RFP 250 ng/10 uL 25 ng/uL 2 700 bp 7 ng 0.3 uL
terminator 5 ng/10 uL 0.5 ng/uL 2 200 bp 2 ng 4 uL
Total 6.3 uL

Ligation and Transformation

Reagent Amount
DNA solution 6.3 uL
Ligation solution 6.3 uL
T4 ligase 1 uL
Total 13.6 uL
  • Incubated at 16C for 30 min
  • Transformation: Added all to 50 uL of competent cell
  • Incubated at 0C for 30 min
  • Heat shocked at 42C for 60 sec
  • 5 min on ice
  • Added 100 uL of LB
  • Incubated at 37C for 120 min
  • Spread onto the LBC plate
  • Incubated at 37C for 20 hrs

RBS Retry

Digestion

Reagent Amount
（RBS）1-2M 10 uL
DW 4 uL
10x M Buffer 2 uL
BSA 2 uL
Xba I 1 uL
Pst I 1 uL
Total 20 uL

->Incubated at 37C for 60 min

Ethanol Precipication

  • Added 2 uL of sodium acetate(3 M)
  • Added 44 uL of Ethanol
  • Transfered to 1.5 mL tube and frozen with liquid nitrogen
  • Melted and centrifuged at 15000 rpm, 4C for 5 min
  • Transfered supernatant to another tube
    • Driven by precaution centrifuged the supernatant and discarded it's supernatant
  • Rinsed the tube walls with 100 uL of 70% Ethanol and centrifuged at 15000 rpm, 4C for 5 min
  • Discarded the supertenant and dried via vacuum desiccator
  • Melted in 5 uL of TE

Electrophoresis

Electrophoresis after Ethanol presipication
  • Added 1 uL of 6x SB to DNA Solution of 1 uL
  • Did the same to supernatant　retreaved for precaution
Lane DNA
2 TSUDA Marker 1
3 supernatant
4 DNA solution
  • DNA solution band is visible
    • Looks OK
Retrieved from "http://2010.igem.org/Team:HokkaidoU_Japan/Notebook/August18"