| Electron Microscopy Unit |
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MAIN AREAS OF
ACTIVITY |
| We apply a combination of high resolution microscopy approaches such as Transmission Electron Microscopy (FEI Tecnai12 TWIN), Scanning Electron Microscopy (Philips XL30) and Laser Scanning Confocal Microscopy (Carl Zeiss LSM 510 META) to address problems in drug discovery research. Mechanisms of cell death in biological systems on drug treatment including morphological and physiological effects are studied. EM experiments are planned, designed, executed and interpreted. Immuno-gold electron microscopy and confocal microscopy are used for sub-cellular localization of biological macromolecules of interest. Significant research contributions have been made in the following areas: |
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Parasite biology – Leishmania cytoskeleton biology; Malaria |
2 |
Mechanism of cell death in human cancer cell lines and in breast cancer explants |
3. |
Mode of action of anti-microbial peptides |
4. |
Intra-cellular distribution of NOS isoforms in rat & human blood cells; NET formation |
5. |
Mitochondrial pathology and dysfunction in gastropathy and in malarial liver damage |
6. |
Evaluation of efficacy, safety and mode of action of spermicidals developed at CDRI |
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| SCIENTISTS
ASSOCIATED WITH THE PROJECT |
| The following scientists
in this Division are associated with this
project. The necessary details in respect
of these scientists are enclosed. Scientists
from other Divisions of the Institute are
also associated with this project. They would
provide this information directly to you. |
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