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Assam Agricultural University, Jorhat

Assam Agricultural University is the first institution of its kind in the whole of North-Eastern Region of India. The main goal of this institution is to produce globally competitive human resources in farm sectorand to carry out research in both conventional and frontier areas for production optimization as well as to disseminate the generated technologies as public good for benefitting the food growers/produces and traders involved in the sector while emphasizing on sustainability, equity and overall food security at household level. Genesis of AAU - The embryo of the agricultural research in the state of Assam was formed as early as 1897 with the establishment of the Upper Shillong Experimental Farm (now in Meghalaya) just after about a decade of creation of the agricultural department in 1882. However, the seeds of agricultural research in today’s Assam were sown in the dawn of the twentieth century with the establishment of two Rice Experimental Stations, one at Karimganj in Barak valley in 1913 and the other at Titabor in Brahmaputra valley in 1923. Subsequent to these research stations, a number of research stations were established to conduct research on important crops, more specifically, jute, pulses, oilseeds etc. The Assam Agricultural University was established on April 1, 1969 under The Assam Agricultural University Act, 1968’ with the mandate of imparting farm education, conduct research in agriculture and allied sciences and to effectively disseminate technologies so generated. Before establishment of the University, there were altogether 17 research schemes/projects in the state under the Department of Agriculture. By July 1973, all the research projects and 10 experimental farms were transferred by the Government of Assam to the AAU which already inherited the College of Agriculture and its farm at Barbheta, Jorhat and College of Veterinary Sciences at Khanapara, Guwahati. Subsequently, College of Community Science at Jorhat (1969), College of Fisheries at Raha (1988), Biswanath College of Agriculture at Biswanath Chariali (1988) and Lakhimpur College of Veterinary Science at Joyhing, North Lakhimpur (1988) were established. Presently, the University has three more colleges under its jurisdiction, viz., Sarat Chandra Singha College of Agriculture, Chapar, College of Horticulture, Nalbari & College of Sericulture, Titabar. Similarly, few more regional research stations at Shillongani, Diphu, Gossaigaon, Lakhimpur; and commodity research stations at Kahikuchi, Buralikson, Tinsukia, Kharua, Burnihat and Mandira were added to generate location and crop specific agricultural production packages.

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20221
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Subject: Veterinary Physiology × Author: Das, Prerana ×
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    ThesisItemOpen Access
    Strategy for development of stem cell like embryonic fibroblast cells
    (College of Veterinary Science, Assam Agricultural University, Khanapara Campus, 2022-09) Das, Prerana; Nath, Nikhil Ch
    Fibroblast cells are the type of cells that play an important role in the formation of connective tissue. The use of fibroblast cell is versatile, for e.g., demonstration of avian viruses, feeder cells, production of vaccines, preservation of genetic resources etc. In this present study, duck embryonic fibroblast cells were isolated, cultured, and sub-cultured up to six passages. The cells were grown in four culture media i.e., Medium 1(MEM), Medium 2(MEM+IGF-1), Medium 3 (MEM+10% FBS), Medium 4 (MEM+10% FBS+IGF-1). In serum and serum-free media the time required for the cells to attain 70% confluence in primary culture was 84.667±.0.152 hours and 111.867±0.161 hours respectively. The cells grown in medium containing serum showed better results than cells grown in serum-free medium. The time taken to reach 70% confluence in 6th passage in Medium 2 and Medium 4 which are IGF-1 supplemented are 94.583±0.217 hours and 62.167±0.096 hours respectively whereas time taken in Medium 1 and Medium 3 which are IGF-1 free media are 95.350±0.039 hours and 62.667±0.152 hours respectively. Therefore, the cells grown in IGF-1 supplemented media showed significant difference compared than the rest of the culture media (p≤0.01). Morphologically, the cells showed characteristic spindle shape, turgor vitalis cytoplasm, centrally located nuclei and flame-like pattern up to the sixth passage. The viability assessment was carried out in first, second, third, fourth, fifth and sixth sub-culture and the viability percentage of the cells in six different sub-cultures were 89.843±0.108, 91.427±0.082, 91.228±0.081, 91.867±0.079, 92.231±0.073, 93.431±0.069 in the case of Medium 1, 90.425± 0.085, 92.358± 0.124, 93.692±0.084, 93.982 ±0.282, 94.625 ±0.089, 94.892 ±0.096 in the case of Medium 2, 89.145 ±0.263, 90.482±0.09, 91.643±0.143, 92.713±0.186, 93.460±0.079, 94.543±0.074 in Medium 3, and 88.597±0.132, 89.387±0.143, 90.552±0.101, 91.423±0.078, 93.077±0.140, 93.077±0.140 in Medium 4. The viability percentage between the passages was significantly different (p≤0.01). However, the viability of the cells was better from the second subculture compared to primary cultures. The pluripotency of the cells was observed by immunostaining using NANOG antibody, a pluripotent marker that is expressed in embryonic stem cells. It was observed that cells showed positive for NANOG at every subculture depicting their pluripotent nature.