IGEM:IMPERIAL/2008/New/Protocols

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= Protocols =
 
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{| cellpadding="1" style="background:#66aadd; border:1px solid #66aadd; color:black" align="left" width=50%
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|width="100%"| <font size=4px><font color=white>'''1. Transformation Protocols for integration vectors in ''Bacillus subtilis'''''
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{{Imperial/Box2|Experiments & Protocols|
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Below you will find a comprehensive list of all the protocols we used during our wet lab work. We spent some time toward the start of the project sourcing and updating effective protocols for ''B. subtilis'' manipulation explicitly, as other teams have previously had difficulty in this area.
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These protocols worked for us, so any future teams looking to use ''subtilis'' could save quite a bit of time by looking here before diving into the literature!}}
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{| cellpadding="1" style="background:#66aadd; border:1px solid #66aadd; color:black" align="center" width=50%
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|width="100%"| <font size=4px color=white>'''1. Transformation Protocols for integration vectors in ''Bacillus subtilis'''''</font>
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*[[/Transformation_protocol_4 | Protocol 2]]
*[[/Transformation_protocol_4 | Protocol 2]]
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|style="background:#66aadd"| <font size=4px><font color=white>'''2. Transformation Protocol for linear DNA in ''Bacillus subtilis'''''
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|style="background:#66aadd"| <font size=4px color=white>'''2. Transformation Protocol for linear DNA in ''Bacillus subtilis'''''</font>
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*Protocol
*Protocol
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|style="background:#66aadd"| <font size=4px><font color=white>'''3. Transformation Protocol ''E.coli'''''
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|style="background:#66aadd"| <font size=4px color=white>'''3. Transformation Protocol ''E.coli'''''</font>
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*[[/XL1-Blue_preparation | Preparation of XL1-blue electrocompetent cells]]
*[[/XL1-Blue_preparation | Preparation of XL1-blue electrocompetent cells]]
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|style="background:#66aadd"| <font size=4px><font color=white>'''4. Motility Analysis'''
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|style="background:#66aadd"| <font size=4px color=white>'''4. Motility Analysis'''</font>
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*[[/Protocols#Motility_Experiments | Motility Assays]]
*[[/Protocols#Motility_Experiments | Motility Assays]]
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|style="background:#66aadd"| <font size=4px><font color=white>'''5. PCR'''
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|style="background:#66aadd"| <font size=4px color=white>'''5. PCR'''</font>
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*[[/Colony_PCR| Single Colony PCR]]
*[[/Colony_PCR| Single Colony PCR]]
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|style="background:#66aadd"| <font size=4px><font color=white>'''6. Calibration Curves'''
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|style="background:#66aadd"| <font size=4px color=white>'''6. Calibration Curves'''</font>
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*[[/Fluorescence| Fluorescence vs GFPmut3b]]
*[[/Fluorescence| Fluorescence vs GFPmut3b]]
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|style="background:#66aadd"| <font size=4px><font color=white>'''7. Promoter-RBS Testing Protocols'''
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|style="background:#66aadd"| <font size=4px color=white>'''7. Promoter-RBS Testing Protocols'''</font>
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*[[/Light_Inducible | Light Inducible Promoters and RBS]]
*[[/Light_Inducible | Light Inducible Promoters and RBS]]
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|style="background:#66aadd"| <font size=4px><font color=white>'''8. Biomaterial Protocols'''
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|style="background:#66aadd"| <font size=4px color=white>'''8. Biomaterial Protocols'''</font>
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*Protocol
*Protocol
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<br clear="all"><br><hr>
{{Imperial/EndPage|Cloning_Strategy|Major_Results}}
{{Imperial/EndPage|Cloning_Strategy|Major_Results}}

Current revision





Experiments & Protocols

Below you will find a comprehensive list of all the protocols we used during our wet lab work. We spent some time toward the start of the project sourcing and updating effective protocols for B. subtilis manipulation explicitly, as other teams have previously had difficulty in this area.

These protocols worked for us, so any future teams looking to use subtilis could save quite a bit of time by looking here before diving into the literature!



1. Transformation Protocols for integration vectors in Bacillus subtilis
2. Transformation Protocol for linear DNA in Bacillus subtilis
  • Protocol
3. Transformation Protocol E.coli
4. Motility Analysis
5. PCR
6. Calibration Curves
7. Promoter-RBS Testing Protocols
8. Biomaterial Protocols
  • Protocol




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