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Gloria Thomas received a B.S. in chemistry (cum laude) from Southern University and A&M College in 1996. She obtained a Ph.D. in analytical chemistry at Louisiana State University and A&M College in 2002. Prior to her appointment as an assistant professor at Mississippi State, Dr. Thomas was a National Research Council Postdoctoral Fellow at the National Institute of Standards and Technology (NIST). |
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Thomas research-group home page telephone: (662) 325-5492 |
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Capillary and Microdevice Technology Development | ||
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Research in my group focuses on developing electrophoretic tools for life
science applications using electrophoresis, the primary
tool of most bioanalytical methods. Using this technique, molecules are separated based upon their size, almost exclusively,
according to the movement of electrically charged particles in a conductive medium under the influence of an applied electric field.
Fabrication of Polymeric MicrodevicesThe terms "microdevice", "microchip", "lab-on-a-chip" and "BioMEMS - biological micro-electromechanical systems" all refer to the small, versatile, inexpensive, fast devices being introduced in many areas of chemistry and life science. They consist of microstructures embedded in glass or plastic and vary from the very simple device consisting of a simple electrophoretic separation channel to the more complex micro-total analysis systems (μTAS). In this format, electrophoretic separation is performed in a microchannel or trough embedded in glass or plastic substrates with wells that serve as reagent and sample reservoirs. Fabrication techniques used include laser ablation, micromilling, injection molding and hot embossing. |
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| Injection zone of a cross-T μdevice. Channels: 50 x 100 μm (W x D) | ||
Other Areas of Research
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Hydrogel Technology | ||
| One area of research in the Thomas Group involves employing photopolymerized polyacrylamide gel plugs in microfluidic channels. Use of these hydrogels allows the physical entrapment of large proteins and/or covalent attachment of DNAs as a conceptually simple method of biomolecule immobilization. In initial studies using simple antibody/antigen models, antigen specific hydrogels were able to capture and concentrate target antigens present at low concentrations with low non-specific binding compared to blank gel plugs. The goal of this project is to apply this concept to relevant models using antibodies, aptamers (antibody-like DNAs) and DNAs. | ![]() | |
| False color image of FITC-labeled antibodies physically immobilized within a microfluidic hydrogel. | ||
Existing Collaborations
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