"
Team:Michigan/Protocols
From 2010.igem.org
(Difference between revisions)
Chillywings (Talk | contribs) (→Protocols) |
|||
| (10 intermediate revisions not shown) | |||
| Line 15: | Line 15: | ||
'''Cell Culture''' | '''Cell Culture''' | ||
| - | [[Media:6-28-2010_Protocol_for_making_cultures_from_a_-80C_freezer_stock.pdf|Making cultures from a - | + | [[Media:6-28-2010_Protocol_for_making_cultures_from_a_-80C_freezer_stock.pdf|Making cultures from a -80°C freezer stock]] |
[[Media:6-29-2010_Making_Frozen_Stoks.pdf|Making frozen stocks]] | [[Media:6-29-2010_Making_Frozen_Stoks.pdf|Making frozen stocks]] | ||
| Line 24: | Line 24: | ||
[[Media:OD600 Cell Dilution Protocol.pdf|OD600 Cell Dilution Protocol]] | [[Media:OD600 Cell Dilution Protocol.pdf|OD600 Cell Dilution Protocol]] | ||
| + | |||
| + | [[Media:Quick Transformation of E. coli Competant Cell Preperation.pdf| Competent Cell Preparation for Quick Transformation of E. coli]] | ||
'''DNA Manipulation''' | '''DNA Manipulation''' | ||
| - | [[Media:Protocol_Heat_Shock_Transformation_2.pdf|Transformation-heat shock]] | + | [[Media:Direct Plating Transformation Protocol.pdf|Direct Plating Transformation Protocol]] |
| + | *Very simple protocol | ||
| + | *Twice as efficient as standard heat shock | ||
| + | |||
| + | [[Media:Protocol_Heat_Shock_Transformation_2.pdf|Transformation - heat shock]] | ||
*Getting parts from the 360 well registry plates | *Getting parts from the 360 well registry plates | ||
| Line 33: | Line 39: | ||
*Heat shock | *Heat shock | ||
| - | [[Media:General_Transformation_Protocol.pdf|Transformation-electroporation]] | + | [[Media:General_Transformation_Protocol.pdf|Transformation - electroporation]] |
*Getting parts from the 360 well registry plates | *Getting parts from the 360 well registry plates | ||
*Competent cell preparation | *Competent cell preparation | ||
| Line 41: | Line 47: | ||
*Adopted from Jeremy Minty's protocol | *Adopted from Jeremy Minty's protocol | ||
*General protocol with specific instructions for ERB/Lin lab equipment | *General protocol with specific instructions for ERB/Lin lab equipment | ||
| + | |||
| + | [[Media:PCR Screening Protocol.pdf|PCR Screening Protocol]] | ||
| + | *Efficient protocol for screening transformants after a ligation | ||
[[Media:MODIFIED_Miniprep_Protocol.pdf|MODIFIED Miniprep]] | [[Media:MODIFIED_Miniprep_Protocol.pdf|MODIFIED Miniprep]] | ||
| Line 51: | Line 60: | ||
[[Media:_Digest_reagents_calculator.xls|Digest Reagents Calculator]] | [[Media:_Digest_reagents_calculator.xls|Digest Reagents Calculator]] | ||
| - | [[Media:Protocol_for_Running_a_Gel.pdf| | + | [[Media:Protocol_for_Running_a_Gel.pdf|Gel Electrophoresis]] |
[[Media:Protocol_for_DNA_Purification.pdf|DNA Purification]] | [[Media:Protocol_for_DNA_Purification.pdf|DNA Purification]] | ||
| Line 68: | Line 77: | ||
[[Media:8-6-2010_Biofilm_Formation_Experiment.pdf|Revised biofilm assay protocol]] | [[Media:8-6-2010_Biofilm_Formation_Experiment.pdf|Revised biofilm assay protocol]] | ||
| - | *[[Media:7-28-2010_Biofilm_Formation_Experiment.pdf| | + | *[[Media:7-28-2010_Biofilm_Formation_Experiment.pdf|Biofilm assay protocol]] |
[[Media:Static+biofilm+quantification.pdf|Alex's biofilm assay protocol]] | [[Media:Static+biofilm+quantification.pdf|Alex's biofilm assay protocol]] | ||
| Line 76: | Line 85: | ||
[[Media:7-31-2010_Ag43_flu_gene_WITH_MODIFIED_PRIMER_SITES.pdf|Detailed primer design]] | [[Media:7-31-2010_Ag43_flu_gene_WITH_MODIFIED_PRIMER_SITES.pdf|Detailed primer design]] | ||
| - | [[Media:8-4-2010_Colony_PCR_flu.pdf| | + | [[Media:8-4-2010_Colony_PCR_flu.pdf|Colony PCR protocol]] |
[[Media:NanR_Cloning.pdf|NanR cloning]] | [[Media:NanR_Cloning.pdf|NanR cloning]] | ||
| Line 85: | Line 94: | ||
====Pili==== | ====Pili==== | ||
[[Media:FimB_Ligation_Protocol.pdf|FimB Ligation]] | [[Media:FimB_Ligation_Protocol.pdf|FimB Ligation]] | ||
| + | |||
| + | [[Media:FimB_PCR.pdf|FimB PCR]] | ||
| + | |||
| + | [[Media:Flocculation_protocol.pdf|Flocculation Protocol]] | ||
====Quorum Sensing==== | ====Quorum Sensing==== | ||
Latest revision as of 00:01, 27 October 2010
Protocols
Using Lab Equipment
Obtaining Deionized Water in the ERB
Enigeering Research Building Autoclave
Epifluorescence Microscope Usage - H.H. Dow
Cell Culture
Making cultures from a -80°C freezer stock
P. putida KT2440 antibotic resistance tolerance
Competent Cell Preparation for Quick Transformation of E. coli
DNA Manipulation
Direct Plating Transformation Protocol
- Very simple protocol
- Twice as efficient as standard heat shock
- Getting parts from the 360 well registry plates
- Competent cell preparation
- Heat shock
Transformation - electroporation
- Getting parts from the 360 well registry plates
- Competent cell preparation
- Electroporation
- Adopted from Jeremy Minty's protocol
- General protocol with specific instructions for ERB/Lin lab equipment
- Efficient protocol for screening transformants after a ligation
Updated T4 DNA Ligase Protocol (Not quick ligase)
- For additional information/questions, refer to [http://www.neb.com/nebecomm/tech_reference/modifying_enzymes/ligation_tips.asp NEB Ligation Tips]
- Ligation
- Ginko Bioworks Protocol
- Jeremy Minty Protocol
Group-Specific Protocols
Oil Sands
Revised biofilm assay protocol
- Updated Colony PCR Protocol
Pili
Quorum Sensing
General Outline for Biobrick Manipulations
