Team:HokkaidoU Japan/Notebook/August16

From 2010.igem.org

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!Amount
!Amount
|-
|-
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|[[Team:HokkaidoU_Japan/Material_And_Methods#Materials_And_Methods|1-1A]]
+
|[[Team:HokkaidoU_Japan/Parts#BioBricks|1-1A]]
|1 uL
|1 uL
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|-
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===Control===
===Control===
* Added 1 uL of 6x Sample Buffer to 1 uL of pUC119
* Added 1 uL of 6x Sample Buffer to 1 uL of pUC119
-
* Also added 1 uL of 6x Sample Buffer to 1 uL of [[Team:HokkaidoU_Japan/Material_And_Methods#Materials_And_Methods|1-1A]]
+
* Also added 1 uL of 6x Sample Buffer to 1 uL of [[Team:HokkaidoU_Japan/Parts#BioBricks|1-1A]]
** Incubated at 37C for 60 min
** Incubated at 37C for 60 min
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|-
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|1
|1
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|[https://2010.igem.org/Image:HokkaidoU_Pictures_DNA_Marker.png Lambda/''Hin''dIII]
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|[https://2010.igem.org/Image:HokkaidoU_Pictures_DNA_Marker.png λ/''Hin''dIII]
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|2
|2
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|3
|3
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|[[Team:HokkaidoU_Japan/Material_And_Methods#Materials_And_Methods|1-1A]] control
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|[[Team:HokkaidoU_Japan/Parts#BioBricks|1-1A]] control
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|4
|4
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|6
|6
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|[Team:HokkaidoU_Japan/Material_And_Methods#Materials_And_Methods|[1-1A]] + Spe I
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|[Team:HokkaidoU_Japan/Parts#BioBricks|[1-1A]] + Spe I
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|7
|7
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!Amount
!Amount
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|[[Team:HokkaidoU_Japan/Material_And_Methods#Materials_And_Methods|1-2M]]
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|[[Team:HokkaidoU_Japan/Parts#BioBricks|1-2M]]
|2.5 uL
|2.5 uL
|-
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|}
|}
</div>
</div>
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<div style="float:left;">
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<div style="float:left; margin-left:50px;">
'''Terminator'''
'''Terminator'''
{|style="text-align: center;" class="protocol"
{|style="text-align: center;" class="protocol"
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!Amount
!Amount
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|-
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|[[Team:HokkaidoU_Japan/Material_And_Methods#Materials_And_Methods|1-23L]]
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|[[Team:HokkaidoU_Japan/Parts#BioBricks|1-23L]]
|1.5 uL
|1.5 uL
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!Amount
!Amount
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|-
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|[[Team:HokkaidoU_Japan/Material_And_Methods#Materials_And_Methods|3-1E]]
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|[[Team:HokkaidoU_Japan/Parts#BioBricks|3-1E]]
|5 uL
|5 uL
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|}
|}
</div>
</div>
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<div style="float:left;">
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<div style="float:left; margin-left:50px;">
'''RFP'''
'''RFP'''
{|style="text-align: center;" class="protocol"
{|style="text-align: center;" class="protocol"
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!Amount
!Amount
|-
|-
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|[[Team:HokkaidoU_Japan/Material_And_Methods#Materials_And_Methods|1-18F]]
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|[[Team:HokkaidoU_Japan/Parts#BioBricks|1-18F]]
|5 uL
|5 uL
|-
|-

Latest revision as of 07:31, 27 October 2010

Notebook

Restriction Enzyme Activity Check

Restriction Enzyme Digestion

EcoR I, Xba I, Pst I

Reagent Amount
pUC119 1 uL
DW 7 uL
10x M Buffer 1 uL
Restriction Enzyme 1 uL
Total 10 uL
  • Made solution for each EcoR I, Xba I, Pst I
    • incubated at 37C for 60 min

Spe I

Reagent Amount
1-1A 1 uL
DW 7 uL
10x M Buffer 1 uL
Restriction Enzyme 1 uL
Total 10 uL
  • pUC119 doesn't have Spe I restriction sites, so we used mini preped plasmid with biobrick insert
    • incubated at 37C for 60 min

Control

  • Added 1 uL of 6x Sample Buffer to 1 uL of pUC119
  • Also added 1 uL of 6x Sample Buffer to 1 uL of 1-1A
    • Incubated at 37C for 60 min

Electrophoresis

Electrophoresis of digested DNA

Added 2 uL of 6x Sample Buffer to digested solution and performed electrophoresis

Lane DNA
1 λ/HindIII
2 pUC119 control
3 1-1A control
4 pUC119 + EcoR I
5 pUC119 + Xba I
6 [1-1A]] + Spe I
7 pUC119 + Pst I
8 Empty

Restriction Enzyme (EcoR I, Pst I) Digestion of the vector

Reagent Amount
pSB1C3 4 uL
DW 10 uL
10x M Buffer 2 uL
BSA 2 uL
EcoR I 1 uL
Pst I 1 uL
Total 20 uL

Restriction Enzyme (Xba I, Pst I) Digestion of the Parts

RBS

Reagent Amount
1-2M 2.5 uL
DW 11.5 uL
10x M Buffer 2 uL
BSA 2 uL
Xba I 1 uL
Pst I 1 uL
Total 20 uL

Terminator

Reagent Amount
1-23L 1.5 uL
DW 12.5 uL
10x M Buffer 2 uL
BSA 2 uL
Xba I 1 uL
Pst I 1 uL
Total 20 uL

Restriction Enzyme (EcoR I, Spe I) Digestion of the Parts

Heat shock promotor

Reagent Amount
3-1E 5 uL
DW 9.7 uL
10x M Buffer 2 uL
BSA 2 uL
EcoR I 1 uL
Spe I 0.3 uL
Total 20 uL

RFP

Reagent Amount
1-18F 5 uL
DW 9.7 uL
10x M Buffer 2 uL
BSA 2 uL
EcoR I 1 uL
Spe I 0.3 uL
Total 20 uL
  • It was obvious after restriction enzyme activity check that Spe I was week, so additional 0.7 uL was added
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