Protocols: Difference between revisions
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(→Yeast) |
(→DNA) |
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[[Agarose Gel]] | [[Agarose Gel]] | ||
[[Annealing Primers]] | [[Annealing Primers]] | ||
[[ | [[Designing Primers]] | ||
[[Ligation]] | [[Ligation]] | ||
[[Library Generation]] | [[Library Generation]] | ||
[[Phosphatase treatment of linearized vector]] | |||
[[PNK Treatment of DNA Ends]] | |||
[[Purification of DNA]] | [[Purification of DNA]] | ||
Revision as of 09:47, 31 May 2005
What is the best way to organize this?
In vivo
Escherichia coli
Yeast
High Efficiency Transformation
T7
Mesoplasma florum
In vitro
DNA
Phosphatase treatment of linearized vector
RNA
Northern Blot, 32P End-Labeled Probes
Probe Prep, 32P End-Labeled Probes
Protein
Microfluidics
Order a Microfluidic Chip from the Foundry
Operate Microfluidic Chemostat
Miscellaneous
Counteracting Evaporation from 96 Well Plates in Long Time Courses on a Victor3 Plate Reader
