Aging Personal Statement Essay

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Personal statement of interest

Aging is a natural process with gradual decrease in vigor, vitality and ultimately leading to death. Imagine adding 20-30 years more to the average life expectancy of humans and promote healthy aging. My interest in aging and age-related diseases first found its root during my undergraduate studies at Aurora's. As part of Biozenith’07, celebrations of 21st century RNA, I presented a paper on 'Aging and Nanobots' and discussed the use of nanobots in age-related diseases such as diabetes, cancer, neurodegenerative disorders and cardiovascular diseases. I want to know how aging plays a crucial role in these diseases. What are the factors that regulate these diseases? Is it possible to diagnose these diseases early? …show more content…

As my masters' progressed, I learned how secondary messenger molecules such as Cyclic AMP, Cyclic GMP, Inositol Triphosphate, Diacylglycerol, and Calcium alter the downstream cellular processes. The conference on Recent Advances in Cardiovascular Sciences and Translational Medicine convinced me that aging and age-related disorders are a consequence of protein signaling networks. I am interested in exploring how molecular and cellular signals, as we age, play a role in cancer and cardiovascular diseases. My masters not only helped me to enhance and share my knowledge, but also get selected for the prestigious Summer Internship at the Centre for Cellular and Molecular Biology …show more content…

Tushar Vaidya, did I receive a fresh impetus for the research. I worked directly with a doctoral student and helped her to know the role of CD40 signaling on the gene involved in the generation of Memory B-cells from naive B-cells on the project 'Cloning and Analysis of the CD40 responsive regulatory regions of the Blimp1 gene of Mouse'. I prepared RPMI media and sub cultured B-Lymphoma cell lines. I learned to design primers for the amplification and cloned 5' upstream flanking region, the promoter, of Blimp1 gene. The obtained constructs were to be introduced into the cell to study expression in response to CD40 treatment.

As my studies progressed, my determination to pursue research had strengthened and I accepted my supervisor's offer to join his lab again as a Dissertation trainee to know the role of Meta1 gene in virulence of Leishmania on the project 'Structure-Function relationship of Meta1 gene in Leishmania'. I prepared different media, carried DNA and RNA isolations, protein induction and purification. I amplified Wild and L58F mutant of Meta1 gene and cloned them into pET expression vector, Induced Protein/ Optimized pET Wild Meta1 and L58F mutant of pET Meta1 and purified

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