Sarah Giuliani
![]() |
Bldg: 202 Room:
A-329 |
> Education:
- 2003, B.S., Purdue (Fort Wayne, IN), Biology with an emphasis in Chemistry
> Professional Experience:
|
Research Assistant in Molecular Biology, Experimental project lead for functional characterization of microbial sensor-type proteins, Biosciences Division, Argonne National Laboratory |
|
Research Assistant in Molecular Biology, DOE Genomes to Life Program (GTL), Biosciences Division, Argonne National Laboratory--specializing in high-throughput protein cloning, expression and purification. |
|
Graduate Research Assistant, Ph.D Program, Supervisor: Dr. Gail B. Mahady, Department of Pharmacognosy,University of Illinois at Chicago (UIC). |
|
Undergraduate Research Assistant in Plant Molecular Genetics, Supervisor: Dr. George S. Mourad, Biology Department, Indiana-Purdue University Fort Wayne (IPFW). |
> Publications:
- Londer, Y.Y., Giuliani, S.E., Peppler,T. and Collart, F.R. Addressing Shewanella oneidensis “cytochromome”: The first step towards high-throughput expression of cytochromes c. Accepted for publication in Protein Expression.
- Giuliani, S.E., Landorf, E.V. and Collart, F.R. 2007. Protein Production for Biotechnology. In: Nature Encyclopedia of Life Sciences. John Wiley & Sons, Ltd, www.els.net.
> Meetings Attended:
- Genomics—GTL Awardee Workshop VI and Metabolic Engineering Working Group Interagency Conference on Metabolic Engineering; 2008 Feb 10–13; Bethesda, MD.
- PepTalk—The Definitive Protein Focused Event. Cambridge Healthtech Institute’s Seventh Annual Conference; 2008 Jan 7-11; San Diego, CA.
- Genomics: GTL Awardee Workshop V and Metabolic Engineering Working Group Interagency Conference on Metabolic Engineering 2007 and USDA-DOE Plant Feedstock Genomics for Bioenergy Awardee Workshop; 2007 Feb 11-14; Bethesda, MD
> Research Interests:
- Characterization of Sensor Proteins and Domains. This project will provide specific functional assignments of proteins by the development of high throughput methods to match ligands with their binding proteins.
- Zebrafish Protein & Antibody Core. This project evaluated strategies for in vitro cloning and production of proteins from Danio rerio. This project is a component of the NIH funded “Zebrafish Protein and Antibody Core” (Brian Kay, PI) which will generate affinity reagents to zebrafish proteins for use by the research community.
- Development of Genome Scale Expression Methods. This program focused on the development of high throughput protein expression methods. A central goal is the distribution of clones and proteins to DOE science programs to insure the appropriate technologies are brought to bear on the scientific problem.
> Research Group:

