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Sarah Giuliani

 

Bldg: 202 Room: A-329
E-mail: sgiuliani@anl.gov
Phone: 630-252-3987
Fax: 630-252-9155

> Education:

  • 2003, B.S., Purdue (Fort Wayne, IN), Biology with an emphasis in Chemistry

> Professional Experience:

  • 2007-present:

Research Assistant in Molecular Biology,  Experimental project lead for functional characterization of microbial sensor-type proteins, Biosciences Division, Argonne National Laboratory

  • 2004 - 2006:
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.
  • 2003 – 2004:
Graduate Research Assistant, Ph.D Program, Supervisor: Dr. Gail B. Mahady, Department of Pharmacognosy,University of Illinois at Chicago (UIC).
  • 1999 - 2003:
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:


U.S. Department of Energy The University of Chicago Office of Science - Department of Energy
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