User:Midori Greenwood-Goodwin: Difference between revisions
No edit summary |
|||
| (19 intermediate revisions by 2 users not shown) | |||
| Line 1: | Line 1: | ||
{{Smolke_Top}} | |||
==Contact Info== | ==Contact Info== | ||
Midori Greenwood-Goodwin <br/> | |||
Stanford Bioengineering - [http://bioengineering.stanford.edu/ Stanford BioE] <br/> | |||
midorigg@stanford.edu | |||
==Education== | |||
B.S. Chemical Engineering, Northwestern University 2007 <br/> | |||
M.S./PhD Bioengineering, 1st Year at Stanford University | |||
== | ==Current Research == | ||
I am working in Sarah Heilshorn's lab on the physical hydrogels project [http://www.pnas.org/content/106/52/22067.full]. My goal is to develop a flexible cloning strategy, as well as test various cell adhesion peptide sequence domains for the hydrogels themselves. | |||
==Research | ==Previous Research == | ||
Worked towards developing a method for high-throughput selection of RNA aptamers to small molecules and proteins using Capillary Electrophoresis - SELEX (Systematic Evolution of Ligands by EXponential enrichment) for integration as sensor domains in engineered riboswitches. | |||
My undergraduate research included work on building virtual instruments for studying DNA single molecule hybridization in microfluidic devices, as well as making polymers and measuring their effect on the observed electroosmotic flow in Capillary Electrophoresis. | |||
==Useful links== | ==Useful links== | ||
[http://www.targetscan.org/ Prediction of miRNA Targets] <br/> | |||
[http://www.ambion.com/techlib/append/na_mw_tables.html DNA and RNA Molecular Weights and Conversions] <br/> | |||
[http://www.neb.com/nebecomm/tech_reference/restriction_enzymes/buffer_activity_restriction_enzymes.asp NEBuffer Activity] <br/> | |||
Latest revision as of 18:24, 6 January 2010
Contact InfoMidori Greenwood-Goodwin EducationB.S. Chemical Engineering, Northwestern University 2007 Current ResearchI am working in Sarah Heilshorn's lab on the physical hydrogels project [1]. My goal is to develop a flexible cloning strategy, as well as test various cell adhesion peptide sequence domains for the hydrogels themselves. Previous ResearchWorked towards developing a method for high-throughput selection of RNA aptamers to small molecules and proteins using Capillary Electrophoresis - SELEX (Systematic Evolution of Ligands by EXponential enrichment) for integration as sensor domains in engineered riboswitches. My undergraduate research included work on building virtual instruments for studying DNA single molecule hybridization in microfluidic devices, as well as making polymers and measuring their effect on the observed electroosmotic flow in Capillary Electrophoresis. Useful linksPrediction of miRNA Targets |
