Team:Northwestern/Protocol

From 2010.igem.org

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[[Team:Northwestern/Protocol/PDNA|Prepping DNA from the kit plates]]
[[Team:Northwestern/Protocol/PDNA|Prepping DNA from the kit plates]]
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[[Team:Northwestern/Protocol/Prepping DNA from the kit plates]]
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[[Team:Northwestern/Protocol/Quikchange (from primers to colonies!)]]
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[[Team:Northwestern/Protocol/Kit to Stock Plasmid]]
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[[Team:Northwestern/Protocol/Ethanol Precipitation]]
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[[Team:Northwestern/Protocol/New Part Design(PCR)]]
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==='''Bacterial Work'''==
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[[Team:Northwestern/Protocol/Transformation]]
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[[Team:Northwestern/Protocol/O/N Culture]]===
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[[Team:Northwestern/Protocol/Preparation of Competent Cells]]
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[[Team:Northwestern/Protocol/LB Media]]
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[[Team:Northwestern/Protocol/Preparing Plates]]
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[[Team:Northwestern/Protocol/Glycerol Stocks]]
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=='''Assembly'''==
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[[Team:Northwestern/Protocol/Restriction Enzyme Digests]]
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[[Team:Northwestern/Protocol/Plasmid Construction]]
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[[Team:Northwestern/Protocol/3A Assembly]]
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[[Team:Northwestern/Protocol/Ligations]]
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[[Team:Northwestern/Protocol/Mini Prep]]
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=='''Microscopy'''==
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[[Team:Northwestern/Protocol/Confocal Microscopy]]
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[[Team:Northwestern/Protocol/Fluorescence Microscopy]]
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=='''Reagents'''==
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[[Team:Northwestern/Protocol/Reagents]]
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=='''Cell Staining'''==
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[[Team:Northwestern/Protocol/Rhodamine-Conjugated Chitin Probe]]
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[[Team:Northwestern/Protocol/Methanol Fixation]]
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==Methanol Fixation==
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[[Team:Northwestern/Protocol/LIVE/DEAD® BacLight - Bacterial Viability Kit]]
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===[[Prepping DNA from the kit plates]]===
===[[Prepping DNA from the kit plates]]===

Revision as of 01:01, 23 October 2010


Tech Institute
Home Brainstorm Team Acknowledgements Project Human Practices Parts Notebook Calendar Protocol Safety Links References Media Contact


DNA

Prepping DNA from the kit plates

Team:Northwestern/Protocol/Prepping DNA from the kit plates

Team:Northwestern/Protocol/Quikchange (from primers to colonies!)

Team:Northwestern/Protocol/Kit to Stock Plasmid

Team:Northwestern/Protocol/Ethanol Precipitation

Team:Northwestern/Protocol/New Part Design(PCR)

=Bacterial Work

Team:Northwestern/Protocol/Transformation

Team:Northwestern/Protocol/O/N Culture===

Team:Northwestern/Protocol/Preparation of Competent Cells

Team:Northwestern/Protocol/LB Media

Team:Northwestern/Protocol/Preparing Plates

Team:Northwestern/Protocol/Glycerol Stocks

Assembly

Team:Northwestern/Protocol/Restriction Enzyme Digests Team:Northwestern/Protocol/Plasmid Construction Team:Northwestern/Protocol/3A Assembly Team:Northwestern/Protocol/Ligations Team:Northwestern/Protocol/Mini Prep

Microscopy

Team:Northwestern/Protocol/Confocal Microscopy Team:Northwestern/Protocol/Fluorescence Microscopy


Reagents

Team:Northwestern/Protocol/Reagents

Cell Staining

Team:Northwestern/Protocol/Rhodamine-Conjugated Chitin Probe

Team:Northwestern/Protocol/Methanol Fixation

Methanol Fixation

Team:Northwestern/Protocol/LIVE/DEAD® BacLight - Bacterial Viability Kit




Prepping DNA from the kit plates

Quikchange (from primers to colonies!)

Kit to Stock Plasmid

Ethanol Precipitation

New Part Design(PCR)

Bacterial Work

Transformation

O/N Culture

Preparation of Competent Cells

LB Media

Preparing Plates

Glycerol Stocks

Assembly

Restriction Enzyme Digests

Plasmid Construction

3A Assembly

Ligations

Mini Prep

Microscopy

Confocal Microscopy

Fluorescence Microscopy

Reagents

Reagents

Cell Staining

Rhodamine-Conjugated Chitin Probe

Methanol Fixation

  1. Rinse slide with ethanol and flame
  2. Rinse slide with PBS and dry with KimWipe
  3. Apply cell sample to microscope slide and let air dry
  4. Submerge in -20C absolute methanol for 5-10 min
  5. Wash 3 times with 1X TBS (submerge in 1X TBS for 5 minutes per wash)
    • Do not let cells dry for the rest of the procedure


LIVE/DEAD® BacLight - Bacterial Viability Kit