Team:Washington/Protocols

From 2011.igem.org

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__NOTOC__
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INSERT INFO HERE... LOOK AT OTHER PAGES FOR EXAMPLES OF FORMATING AND INSERTING PICTURES.  CLICK THE EDIT BUTTON ON THE UPPER LEFT SIDE OF THE PAGE AFTER YOU HAVE SIGNED IN.
 
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[https://2011.igem.org/Team:Washington/Alkanes/Protocols/Example_1 Example 1]
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=General Protocols=
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[https://2011.igem.org/Team:Washington/Alkanes/Protocols/Example_2 Example 2]
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[https://2011.igem.org/Team:Washington/Protocols/PCR  General PCR Protocol]
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[https://2011.igem.org/Team:Washington/Protocols/Digestion  General Digestion Protocol]
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[https://2011.igem.org/Team:Washington/Protocols/Ligation  General Ligation Protocol]
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[https://2011.igem.org/Team:Washington/Protocols/Transformation  General Transformation Protocol]
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[https://2011.igem.org/Team:Washington/Protocols/Colony Colony PCR Protocol]
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[https://2011.igem.org/Team:Washington/Protocols/Competent  Competent Cell Prep Protocol]
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Check out or add wiki design tools here:
 
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[https://2011.igem.org/Team:Washington/Protocols/Wiki_Design Wiki Design]
 
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[http://www.bio.davidson.edu/Courses/molbio/kunkel/kunkel.html Overview of how Kunkel Mutagensis works]
[http://www.bio.davidson.edu/Courses/molbio/kunkel/kunkel.html Overview of how Kunkel Mutagensis works]
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[https://2011.igem.org/Team:Washington/Protocols/plate_expression 96 Well Plate Protein Expression]
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[https://2011.igem.org/Team:Washington/Protocols/expression_purification Standard 1L Expression Purification]
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[https://2011.igem.org/Team:Washington/Protocols/gene_assembly Gene Assembly With Oligos]
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[https://2011.igem.org/Team:Washington/Protocols/CompDesign Computational Protein Design]
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=Make It:  Diesel Production Protocols=
[https://2011.igem.org/Team:Washington/alkanebiosynthesis Alkane Biosynthesis media and extraction]
[https://2011.igem.org/Team:Washington/alkanebiosynthesis Alkane Biosynthesis media and extraction]
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[https://2011.igem.org/Team:Washington/Protocols/expression_purification Standard 1L Expression Purification]
 
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[https://2011.igem.org/Team:Washington/Protocols/gene_assembly Gene Assembly With Oligos]
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=Break It: Gluten Destruction Protocols=
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[https://2011.igem.org/Team:Washington/Protocols/Cell_Lysate_Assay Cell Lysate Assay]
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[https://2011.igem.org/Team:Washington/Protocols/50mL_Scale Small Scale (50mL) Protein Expression and Purification]
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=Magnets Protocols=
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=Gibson Vectors (pGB) protocols=
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Check out or add wiki design tools here:
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[https://2011.igem.org/Team:Washington/Protocols/Wiki_Design Wiki Design]
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=Protocol Page=
 
'''restriction digest'''
'''restriction digest'''

Revision as of 16:42, 12 September 2011



General Protocols

General PCR Protocol

General Digestion Protocol

General Ligation Protocol

General Transformation Protocol

Colony PCR Protocol

Competent Cell Prep Protocol


Kunkel Mutagensis

[http://www.bio.davidson.edu/Courses/molbio/kunkel/kunkel.html Overview of how Kunkel Mutagensis works]

Standard 1L Expression Purification

Gene Assembly With Oligos

Computational Protein Design


Make It: Diesel Production Protocols

Alkane Biosynthesis media and extraction


Break It: Gluten Destruction Protocols

Cell Lysate Assay

Small Scale (50mL) Protein Expression and Purification


Magnets Protocols

Gibson Vectors (pGB) protocols

Check out or add wiki design tools here: Wiki Design


restriction digest 10 uL DNA

5uL buffer ( 2 for most, check http://www.neb.com/nebecomm/DoubleDigestCalculator.asp)

.5 uL BSA

1uL enzyme 1

1uL enzyme 2

water to 50 uL(32.5 uL, add first)

oligo assembly by PCR

resuspend oligos with water, amount of water= concentration(in nm)*10 in uL

make oligo mix with 5uL of each primer

PCR reaction: 1uL phusion

.5uL oligo mix

1uL first oligo

1uL last oligo

5uL buffer

1uL dnTP

dH20 to 50uL

Ligation

7uL insert

1uL vector

1uL T4 ligase buffer

1uL T4 ligase

incubate at 37C no. **Note that NEB website recommends 16C - room temp for ligations, we do ours at RT and it works well. 1 hour.

Colony PCR with Green tag

Master mix(7ul):

1ul 10uM forword primer

1ul 10uM reverse Primer

5ul 2x Green tag

Cell water(3ul): Pick one colony from the plate and mix with 10ul of ddH2O to make 10ul of cell water

Reaction = Master mix(7ul) + Cell water(3ul) = 10ul per tube

Use program "Colony" & change the extention time (1min per kb)

Heat Shock Transformation

2 ul ligation

20 ul cells

Ice 20 minutes

Heat shock at 42C for 1 minute

Ice 2 minutes

Prepare 200 ul of TB (no anti) and transformed cells in culture tube

Incubate at 37C for 1 hour

Plate cells

Retrieved from "http://2011.igem.org/Team:Washington/Protocols"