Animal Biotechnology

The objectives of the Centre are:

  • To undertake biotechnology-oriented basic and applied research programmes for improving animal productivity and for developing innovative dairy processes for producing superior quality, safe and wholesome dairy products,
  • To train manpower for the application of biotechnology for dairy production and dairy processing and
  • To organize M.Sc./M.V.Sc./M.Tech and Ph.D. programmes in animal biotechnology at NDRI (Deemed University).
Dr. Suneel Kumar Onteru, HOD

Dr. J.K. Kaushik, HOD

Research work in various laboratories at the Animal Biotechnology Centre is focused on three main areas namely embryo biotechnology, animal genomics and proteomics & structural biology. Major areas of interest in embryo biotechnology include in vitro embryo production, animal cloning, production of transgenic animals, embryonic and adult stem cells and cryopreservation of gametes. The Centre holds the distinction of producing world’s first IVF buffalo calf, world’s first buffalo calf produced through Hand-made cloning and India’s first goat kid produced by IVF. The focus of research in animal genomics is on understanding animal reproduction at molecular level, studying the role of miRNAs and remodeling sperm surface for improving reproductive efficiency in buffalo. The Centre has developed PCR-based assays, many of which have been patented. The focus in proteomics is on development of diagnostic kits for early pregnancy detection and identification of subclinical mastitis, and understanding proteomics of milk production and lactation. Another area of interest is to develop novel inexpensive technology for sexing of semen. The structural biology research is aimed at development of bioactive recombinant proteins for human use. In addition to these, the Centre has a laboratory on bioinformatics. Some other areas of research are understanding antibiotic resistance in mastitis-causing bacteria and the use of mesenchymal stem cells for treatment of diseases in dairy animals.

Currently, we have 13 externally-funded research projects funded by DBT, ICAR-NASF, SERB-DST and Bill & Melinda Gates Foundation, USA with the more than 14 crores of funds. Besides these, there are several in-house research projects funded by NDRI. The Centre has the distinction of publishing a large number of research papers every year in scientific journals having high impact factor.

The Centre offers Masters and Doctorate (Animal Biotechnology) degree programs to cater to the need of scientists and researchers in the field of dairy, animal and veterinary sciences in ICAR institutes, agricultural universities and, state and central govt. funded institutions. A summer training program is organized every year to provide on-bench training to post-graduate students of biotechnology from all over India. Currently the Centre has 10 faculty members, 38 M.Sc., M.Tech. and M.V.Sc. students, 75 Ph.D. students, 20 JRFs, SRFs and Research associate, and 4 Post-doctoral researchers and Young Scientists are working at the centre.

I invite you to explore our Institute web site, www.ndri.res.in to learn more about the faculty, research facilities, students, teaching programs and ongoing research projects at the Animal Biotechnology Centre.

For more information, please contact: Dr. S. De
Principal Scientist & Officer In-Charge
Animal Biotechnology Centre
ICAR-NDRI Karnal - 132001
Haryana, India

Sr. No. Faculty Name Designation
1 Dr. Jai Kumar Kaushik Principal Scientist
2 Dr. Dhruba Malakar Principal Scientist
3 Dr. Manoj Kumar Singh Senior Scientist
4 Dr. Rakesh Kumar Principal Scientist
5 Dr. Sachinandan De Principal Scientist
6 Dr. Satish Kumar Principal Scientist
7 Dr. Sudarshan Kumar Senior Scientist

Research activities in animal biotechnology were initiated at NDRI, Karnal during mid-80s with the establishment of a UNDP 'Centre of Excellence on Biotechnology' program in view of the need to utilize biotechnology as a means to transform the agriculture scenario in India. An urgent need for development of biotechnological interventions for improving reproduction and productivity of dairy animals provided the basis for the establishment of Embryo Biotechnology Centre (EBC) at NDRI Karnal by financial support from the Dept. of Biotechnology, Govt. of India. Subsequently, EBC was further strengthened by the establishment of Livestock Genome Laboratory and Molecular Biology Unit under the National Agricultural Research Project-II of ICAR. Animal Biotechnology Centre was reorganized in June 1999 by consolidating all the infrastructure facilities created under various programs on biotechnology at NDRI, Karnal and getting them under one umbrella. A state-of-the-art facility was created in 2007 to consolidate research and teaching activities in biotechnology at the new building of Animal Biotechnology Centre. The new building offers a working space of more than 20,000 sq. ft.

The objectives of the Centre are:

  • To undertake biotechnology-oriented basic and applied research programmes for improving animal productivity and for developing innovative dairy processes for producing superior quality, safe and wholesome dairy products,
  • To train manpower for application of biotechnology for dairy production and dairy processing and
  • To organize M.Sc./M.V.Sc./M.Tech and Ph.D. programmes in animal biotechnology at NDRI (Deemed University).

Master's courses

Sr. No.CodeCourse TitleAims
1BT 611Fundamentals of cell & molecular biology (3+0)Molecular structure and functions of cells and molecules such as DNA, RNA and proteins.
2BT 612Animal cell culture: principles & applications (2+1)Understanding the principles of animal cell culture and its application
3BT 613Immunology applied to biotechnology (2+1)Understanding the application of immunological techniques in biotechnology.
4BT 614Reproductive biotechnology (2+1)Understanding in-vitro reproductive techniques for ovum and embryo manipulation.
5BT 621Applied molecular biology (2+1)Understanding the principle and application of recombinant DNA in biotechnology.
6BT 622Molecular diagnostics (1+2)Understanding the molecular techniques involved in diagnosis of diseases.
7BT 623Animal genomics (2+1)Understanding structural, functional and comparative genomics of farm animals and its application for livestock improvement
8BT 624Techniques in molecular biology & genetic Engineering (0+3)To provide comprehensive hands-on training on techniques of molecular biology and genetic engineering.
9BT 629Master's Seminar (1+0)-
10BT 639Master's Research (20)-

Ph.D. Courses

Sr. No.CodeCourse TitleAims
1BT 711Gene cloning and expression (3+0)Understanding the concept of gene cloning and expression.
2BT 712Functional genomics & proteomics (3+0)Understanding gene expression at different conditions/organs
3BT 713Advances in reproductive biotechnology (3+0)Understanding the new developments in reproductive technology.
4BT 719Doctoral seminar (1+0)-
5BT 721Trends in Vaccinology (3+0)Understanding the latest developments in vaccine production technologies.
6BT 722Advances in animal cell culture (3+0)Understanding the latest developments in cell culture techniques.
7BT 729Doctoral Seminar II (1+0)-
8BT 739Doctoral Research (20)-

Our research activities are focused on four major areas namely the embryo biotechnologies, animal genomics, proteomics & system biology and stem cell biology. Faster multiplication of superior germplasms of dairy animals by the application of hand-made cloning technology remains one of the prime areas of our current research. Identification of superior animals utilizing the candidate genes/proteins related to economic and physiological traits of dairy animals ensuring faster genetic gains in animals and development of the selection criteria for dairy animal is the other major area. Fundamental knowledge of one gene synthesizes many proteins is being investigated at the centre to assess the economic traits of dairy animals by utilizing in vitro embryo production system followed by the molecular investigations. Exploring the reproduction traits and disease resistance qualities of Indian dairy breeds are the current interests of the research groups. Proteomics is another branch of the functional genomics, responsible for improvement of dairy production, productivity and processing areas. With the introduction of high-throughput and cutting-edge technology of mass-spectrometry for proteomic studies, the researchers at center are generating the proteomic profile of sub-clinical mastitis and matritis diseases. Early detection of pregnancy utilizing PAGs and miRNA are also being investigated at the center. Development of recombinant proteins as the intermediate technologies for fulfilling the needs of the animal and dairy industry forms another major area of research at ABTC. Many such useful recombinant proteins such as LIF, GDF-9, Lectoferrin, SSLP and amino-peptidases have been developed in the recent past. Researchers at the centre are also engaged in promoting development of designer animals and humanized dairy milk from animals by utilizing CRISPER and TALEN based genome editing tools. In the era of high usage of antibiotics in dairy industry, stem cell technology has emerged as an alternative to treatment with antibiotics for diseased udder, skin and hoof wounds. Mesenchymal stem cell technology has been developed at the centre and routinely utilized for treatment of animal diseases.

The state of art laboratories equipped with modern and high end equipments and tools are available at ABTC to carry out all research activities. The laboratories are equipped with equipments like LC-MS/MS, Flow cytometer with sorter, Bioreactors, DNA sequencer, Real-time PCR, Micromanipulator and range of incubators and freezers. A specialized bioinformatic facility is available to cater the need of researchers for studying the niche areas of bioinformatics related to animal biotechnology.

Patents

  • A non-invasive DNA isolation methodology in Dairy Animals. (Application No-1366/Del/2007). Patent Grant Date: 31-01-2014.
  • A PCR based method for differentiating Cow and Buffalo milk (No-011-020181 dated 22/11/2013).

Technologies

  • DNA based method for differentiation of cow & buffalo meat, ghee, butter, milk and milk products.
  • Universal cell lysis solution for direct PCR from animal, plant tissues and bacterial cells.
  • A PCR (polymerase Chain Reaction) based A1/ A2 beta casein genotyping method for milk and milk product.
  • Development of mesenchymal stem cells from adipose issues for treatment of wound, paralysis, fracture, mastitis, endometritis and cancer in animals.
  • Generation of oocytes from embryonic and induced pluripotent stem cells.

List of externally funded projects (as on March 6, 2019)

Sr. No.Project NameFunded ByDurationProject Leader
1Deciphering the circulating miRNAs from terminal stage pre-implantation embryos and placentomes for early detection of pregnancy in buffaloDBT, Govt. of India: Rs. 52.2715 lakhs4.8.2016 to 3.7.2019Dr. T. K. Datta,
Co-Leaders : Dr. Rakesh Kumar and Dr. A. Kumaresan
2Synthesis, characterization and effect of graded levels of nano-selenium supplementation on the performance of broiler chickenICAR-NASF: Rs. 42.727 lakhs1.6.2017 to 31.5.2020Dr. A.K. Mohanty,
Co-Leaders : Dr. Sudarshan Kumar
3Genetic variability of milk protein and its characterization by proteomic approach in Indian goatsICAR-NASF: Rs. 34.45080 lakhs1.6.2017 to 31.5.2020Dr. S. De
4Conservation of Indigenous Pig of Assam through Handmade Cloning TechniqueDBT, Govt. of India: Rs. 40.59 lakhs2.1.2017 to 1.1.2020Dr. M. K. Singh
5Global transcriptome and miRNA analysis for deciphering reasons for low cloning efficiency in buffaloSERB, DST, Govt. of India: Rs. 46.78 lakhs22.3.18 to 21.3.21Dr. P. Palta,
Co-Leaders : Dr. M. K. Singh
6Production of multiple copies of elite buffalo bulls using animal cloning technologyICAR-NASF: Rs. 264.2964 lakhs31.3.2018 to 30.3.2022Dr. P. Palta,
Co-Leaders : Dr. M. K. Singh, Dr. S. S. Lathwal, Dr. Subhash Chand
7Genome editing of MFGE8 and S100 genes in bovine mammary epithelial cells to understand their role in milk productionSERB, DST, Govt. of India; Rs. 62.538 lakhs21.3.2018 to 20.3.2021A. K. Mohanty,
Co-Leaders : Dr. Sudarshan Kumar, Dr. J. K. Kaushik, Dr. Malakar, Dr. Satish Kumar
8Improving the usability of buffalo spermatozoa by sperm surface remodelling and immune acceptance in female reproductive tractICAR-NASF: Rs. 174.60 lakhs1.7.2018 to 30.7.2021Dr. T. K. Datta,
Co-Leaders : Dr. Rakesh Kumar, Dr. J. K. Kaushik
9Molecular Markers for Improving Reproduction of Cattle and BuffaloesBill & Melinda Gates Foundation, USA: Rs. 648.38 lakhs31.07.2018 to 31.07.2023Dr. T. K. Datta,
Co-Leaders : Dr. Rakesh Kumar, Dr. Dheer Singh, Dr. Suneel Onteru, Dr. R. K. Baithalu, Dr. A. K. Mohanty, Dr. Sudarshan Kumar, Dr. T. K. Mohanty
10Targeted immobilization of Y-bearing spermatozoa and modulation of oviduct milieu for skewing sex ratio towards female offspring in dairy cattleICAR-NASF: Rs. 11.34 lakhs01.08.2018 to 31.07.2021Dr. Rakesh Kumar,
Co-Leaders : Dr. T. K. Datta
11CRISPR/CAS9 guided functional analysis of genes regulating early embryonic survival in buffaloICAR-NASF: Rs. 62.4431 lakhs01.08.2018 to 31.07.2021Dr. Dhruba Malakar,
Co-Leaders : Dr. Satish Kumar
12Development of early pregnancy diagnostic assay through discovery of biomarkers in cattle and buffaloDBT, Govt. of India: Rs. 114.70725 lakhs10.5.2018 to 9.5.2021Dr. A. K. Mohanty,
Co-Leaders : Dr. R. K. Baithalu, Dr. T. K. Mahanty, Dr. Sudarshan Kumar
13Semen sexing in cattleICAR: Rs. 239.5 lakhs1.4.2017 to 31.3.2021Dr. A. K. Mohanty,
Co-Leaders : Dr. Sudarshan Kumar

PDF Projects

Sr. No.Project NameProject ByDuration YearProject Workers
1Quantitative profiling of buffalo milk fat globule membrane, a promising nutraceutical for infant formula milkWoman Scientist Scheme of DST)2017-20A. Turan, J. K. Kaushik
2Profiling of milk proteome in different species of farm animals and comparative evaluation of host defense proteinsNPDF project2016-18A. Chopra, A. K. Mohanty
3Protein profiling of semen of cross-bred cattle bulls for identification of biomarkers for high semen freezabilitySERB-NPDF2017-2019S. Kalra, A. K. Mohanty
4Pesticide exposure and sperm fertilizing ability: A study on Bovine ModelSERB-PDF2018-20Shivani Chhillar and T. K. Datta
5Delineating genome wide methylation dynamics in cows of native and exotic origin: An approach to understand heat stress adaptationSERB-PDF2018-20Preeti Verma and A. K. Mohanty
6Development of methods for detection of betacasomorphin-7 in biological samples, (urine or blood) by aptamersICMR-RA2018-21Abhishek and A. K. Mohanty

  • A male cloned calf named 'Rajat', was born on July 23, 2014 by normal parturition. Rajat was produced through Hand-guided cloning using somatic cells isolated from the frozen-thawed semen of a highly ranked progeny-tested Murrah buffalo bull (MU-4393) which had died many years back.
  • A female calf named 'Deepasha' was born on December 12, 2014 by normal parturition. Deepasha is a clone of a wild buffalo named 'Asha', that has been kept in semi-captivity at Chhattisgarh. The wild buffalo is an endangered species.
  • A female cloned calf named 'Apurva' was born on February 5, 2015 through normal parturition. Apurva was produced using somatic cells isolated from urine.
  • A female cloned calf named 'Lalima' was born on May 2, 2014 by normal parturition. Lalima is a clone of an elite Murrah buffalo (MU-5345) of NDRI Livestock Farm.
  • Garima II, the cloned buffalo, delivered second female calf named 'Karishma' on December 27, 2014 through normal parturition.
  • A female cloned calf named 'Swarupa' produced through 'Hand-guided Cloning' was born on August 1, 2015. Swarupa is a clone of 'Karan-Kirti', the highest milk producing Murrah buffalo at NDRI Livestock Research Centre.
  • Transgenic buffalo and goat embryos containing human insulin gene were produced from transfected buffalo fetal fibroblasts.
  • Germ line cell-specific genes were identified in buffalo and buffalo embryonic stem cell lines were differentiated towards germ lineage.
  • VASA-transgenic buffalo embryonic stem cell lines were established and differentiated to germ lineage.
  • Global transcriptome profiling was carried out in goat embryos at different stages of development, produced by in vitro fertilization, somatic cell nuclear transfer and parthenogenesis.
  • Buffalo recombinant interferon-tau was produced.
  • Cloning work at NDRI was highlighted as 9th among top 20 science stories of 2014 by 'Scientific India', a science magazine.
  • Cloned buffalo embryos were successfully produced using trophoblast cells, urine and milk-derived somatic cells and lymphocytes as donor cells.
  • Cloned blastocysts derived from fibroblasts, milk-derived cells, lymphocytes, trophoblast cells and those produced by in vitro fertilization were found to differ in their developmental competence, level of apoptosis, epigenetic status and expression level of many important genes.
  • Buffalo trophoblast cell lines were developed from blastocysts produced by in vitro fertilization, Hand-guided cloning and parthenogenesis. A feeder-free in vitro culture system was developed which enabled their long-term culture.
  • Treatment of buffalo donor cells with epigenetic modifiers was shown to improve the blastocyst rate and quality of cloned embryos
  • Cloned female and male buffalo embryos were found to differ in their developmental competence, epigenetic status, sex-biased transcription patterns in X-linked genes and response to epigenetic modifiers. Aberrant X-linked gene expression occurred frequently in female embryos.
  • Transgenic cloned buffalo embryos were produced containing pAcGFP-buSCD, a mammary gland specific expression vector, which is able to convert high level of conjugated linoleic acid in mammary gland epithelial cells.
  • Global transcriptome and miRNA profiling was carried out in buffalo blastocyst-stage embryos produced by cloning and in vitro fertilization techniques to identify the shortcomings with cloned embryos. This will help in making strategies for improving the success rate of producing cloned calves in cattle and buffaloes.
  • Transgenic buffalo spermatogonial stem cells were produced and used for homologous transplantation.
  • Mammary lineage cells were produced by directed differentiation of buffalo embryonic stem cells.
  • Novel non-coding RNAs were discovered in buffalo oocytes which may influence their development competence.
  • Recombinant bovine lukemia inhibitory factor was produced successfully. Its use as a supplement for culture of bovine stem cells may help improve efficiency and reduce the cost.
  • Direct application of mesenchymal stem cells isolated from adipocyte tissue was demonstrated to be effective in management of chronic hoof wounds in cattle and buffaloes.
  • Treatment of human intestinal cells with recombinantly produced lactobacilli surface layer proteins could prevent pathogen binding to the extent of as high as 76%.
  • Application of pulsed electromagnetic field to reconstructed embryos during Hand-guided cloning was shown to increase the blastocyst production rate and improve the quality of cloned embryos produced.
  • Transgenic goat embryos, having GFP integration at Rosa 26 locus, were produced using one of the latest genome editing tools Transcription Activator-like Effector Nucleases (TALEN).
  • Tetraploid complementation with putative parthenogenetic embryonic stem cells was successfully used for production of chimeric blastocyst-stage goat embryos.
  • Treatment of cloned embryos with miR-145 inhibitor was shown to improve their developmental competence and quality, and increase histone acetylation and expression level of several pluripotency-related genes.
  • A novel non-coding RNA (BOA 290U) was identified in buffalo oocyte and its association was established with expressed proteins. It is potentially important for imparting developmental competence to oocytes.
  • The chronology of GVBD event was found to be associated with competence of buffalo oocytes. Holding oocytes temporarily at GV stage was found to be useful in enhancing their developmental ability.
  • High throughput RNA sequencing of buffalo oocytes revealed genes which are significantly affected in 'Good' vs. 'Bad' oocytes. Affected pathways in inferior quality oocytes were identified.
  • A battery of unique non-coding mi & pi RNAs was discovered in buffalo oocytes, which could be linked to their competence. Major genes under CLR and NLR category were amplified and sequenced completely.
  • Basal expression pattern of important RLR, NLR and CLR genes was compared in immune and non-immune buffalo tissues. A large number of splice and transcript variants were observed to be present under RLR, NLR and CLR category in different types of buffalo tissues.
  • Potential protein biomarkers have been identified in urine and serum of cows for early detection of pregnancy 16 days post artificial insemination.
  • A proteomics-based method was developed for detection of A1/A2 milk of cattle and buffaloes
  • Candidate microRNAs, which were uniquely expressed during early pregnancy (30 days) in buffalo, were identified.
  • Specific miRNAs associated with maternal and fetal placentomes were identified in early pregnant buffaloes. A step towards detection of pregnancy by miRNAs.
  • Comparative sequence analysis of β-defensins from different species by bioinformatic analysis revealed that buffalo β-defensins have unique conserved functional motifs although their sequences are quite different from those of other closely related mammals.
  • Increased expression of sperm coat protein, beta-defensins 126 and 129 was detected in epididymis of buffalo testes.
  • Eight novel variants of goat kappa casein variants were revealed from seven different Indian goat breeds.
  • Functional characterization of Milk fat globule membrane epidermal growth factor 8 was performed by gene silencing using shRNA. It was observed that MFGE8 is essential for maintenance of cell shape and morphology during lactation in farm animals.
  • A total of 1600 proteins were identified in bovine urine by using LC-MS/MS for the first time. Various methods were optimized for extraction of proteins from bovine urine.
  • Three potential urine protein biomarkers (bovine allergen, Mannan-binding lectin serine peptidase 2, Alpha-1-microglobulin, Glutaminyl-peptide cyclo-transferase) were identified for detection of early pregnancy (~ 20 days) in cows. Three proteins namely vitamin-binding protein, apolipoprptein A and complement 3 were up-regulated in bovine serum during pregnancy (16th to 45th day).
  • Differential transcript analysis in fetal cotyledon of early pregnant buffalo (~2 months) revealed that prostate-specific antigen is over-expressed during early pregnancy.
  • Recombinant leucyl aminopeptidase of Lactobacillus species was expressed in biologically active form.
  • Buffalo hepatocytes were successfully cultured for over a week on several extracellular matrices and feeder fibroblast cells.
  • Methods were standardized for in vitro differentiation of buffalo mammary epithelial cells for expression of milk proteins (casein).
  • The function of MGP-40, a mammary-specific protein which protects the loss of mammary epithelial cells during mammary gland involution via activation of STAT-3 phosphorylation, was deciphered.
  • Buffalo oviductin was observed to have a positive effect on several sperm quality-related parameters such as motility, viability, acrosomal integrity and capacitation. Oviductin was found to increase cleavage rate and blastocyst formation during IVF.
  • Salivary proteome of Sahiwal cows revealed 3000 proteins, which is the highest number reported hitherto.
  • A stably transfected COS-1 cell line was established which expressed recombinant buffalo leukemia inhibitory factor.
  • Recombinant buffalo GDF9 (57 kDa) was shown to enhance cleavage and blastocyst rate during production of IVF buffalo embryos.
  • Recombinant mucus binding protein (rMub), S-layer protein (rSlp) of lactic acid bacteria were shown to preclude the binding of enterotoxigenic coli (ETEC) with human enteric cell lines Caco-2 and HT-29.
  • Recombinant leucyl aminopeptidase and prolyl aminopeptidase of lactobacilli origin were expressed, their physicochemical properties studied and their specific activity was shown to be better or comparable to that of commercially available Corolase enzyme.
  • Proteins differentially expressed in milk whey of A1 and A2 milk were identified for analyzing their health implications
  • New definition of precious pashmina fibers was established with its unique proteomic compositions. Key proteins involved in Pashmina fibre growth and development were identified by analysis of Pashmina fibre and skin proteome.Around 7000 proteins were identified in the skin proteome of Pashmina goats
  • A proof-of-concept was developed for the detection of pregnancy in cattle, as early as 35 days, using an antibody against Pregnancy Associated Glycoprotein-7 (PAG7).
  • A LC-MS method was developed for identification of A1 and A2 beta caseins in milk of Karan Fries and Sahiwal cattle. The method has been validated in more than 200 cows.
  • More than 6800 proteins were identified for the first time in milk of Sahiwal cattle.
  • 1371 differentially expressed genes and 757 differentially expressed proteins were identifies during lactogenic differentiation in buffalo mammary epithelial cells and their possible role in lactation was studied.
  • A stably transfected COS-1 cell line was developed which expresses recombinant bovine Leukemia Inhibitory Factor .
  • Mesenchymal stem cells used successfully to permanently cure hoof wounds in cattle and buffaloes.
  • Mouse allogenic and cattle xenogeneic mesenchymal stem cells were used to successfully heal fractured tibial bones of mice within 5 weeks.
  • Recombinant buffalo sperm lysozyme like protein 5 (SPACA5) was produced using coli expression system.
  • More than 12000 proteins have been profiled in Buffalo mammary epithelial cells, and 6 novel proteins were found to be involved in lactogenesis.
  • Three different isoforms of buffalo pregnancy associated glycoproteins (PAG-1, PAG-2 & PAG-18) were produced in coli expression system.
  • An innovative microfluidic device was developed for partial enrichment of live and motile sperm cells.
  • Mesenchymal stem cells were successfully used to cure mastitis and metritis in cattle.

Sr. No.Name of the Student Passed OutGuideMSc/MVSc/MtechYear Passed OutCurrently atEmail
1Mr. S. K. DasS L GoswamiMSc1991-subratakdas1[at]gmail[dot]com
2Ms. H. S. LalithaS L GoswamiMSc1996--
3Ms.Parul MannS L GoswamiMSc1996--
4Mr. Imtiaz ZafarS L GoswamiMSc2000-imtiaz[dot]ncbs[at]gmail[dot]com
5D. VasanthD. MalakarM. Sc.2004Guest Faculty at the Department of Microbial Biotechnology, Bharathiar University, Coimbatore-641046, Tamil Naduvasanthguy[at]gmail[dot]com
6Aravindhan G. N.T K DattaM.V.Sc.2004-arvindhan[dot]nagarajan[at]yale[dot]edu
7Ms. Kamna SinghS L GoswamiMSc2004--
8Ajay Pal Singh AswalT K DattaM.V.Sc.2005-aswal_aps[at]rediffmail[dot]com
9Dr. Sudarshan KumarJ. K. KaushikMVSc2005ARS Scientist, Animal Biotechnology Centre, National Dairy Research Institue, Karnalkumarsudershan[at]gmail[dot]com
10Dr. Sachin S. PawarD. MalakarM.V. Sc.2006Scientist (Animal Biotechnology) National Institute of Abiotic Stress Management Malegaon Baramati 413 115, District Punesachinndri[at]gmail[dot]com
11Dr. Arun Kumar DeD. MalakarM. V. Sc.2007Scientist (Animal Biotechnology) ICAR-Central Island Agricultural Research Institute, Port Blair, Andaman and Nicoborbiotech[dot]cari[at]gmail[dot]com
12Aditya Prasad SahooT K DattaM.V.Sc.2007Scientist, National FMDCP Seromonitoring Laboratory, ICAR-DFMD, Bengalururush2aditya[at]gmail[dot]com
13Ms. Moloya GohainS L GoswamiMSc2008-moloyandri[at]gmail[dot]com
14Dr. Anoop J.J. K. KaushikMVSc2008Manager, KLD Board, Mattupatty, Munnar, Idukki, Keralajanoop73[at]gmail[dot]com
15Dr. Manoj Kumar JenaD. MalakarM. V. Sc.2009Assistant Professor, Department of Biotechnology School of Bioengineering and Biosciences, Lovely Professional University, Jalandhar, Punjabdrmanoj[dot]jena[at]gmail[dot]com
16Kumari Arpana VermaT K DattaM.V.Sc.2009ICMR Postdoctoral fellow NIRRH,Mumbai,Indiaarpanandri[at]gmail[dot]com
17Mr. Guru PrasadS L GoswamiMSc2009--
18Dr. Rahul DuttaD. MalakarM. V. Sc.2010Grants Adviser, Well come/DBT India Alliance, Hyderabaddoctordut[at]gmail[dot]com
19Sandeep KumarT K DattaM.V.Sc.2010Senior Scientist, Xcelris Labs Ltd., Ahmedabadsandeepndribiotech[at]gmail[dot]com
20Gattu RudrappaJ. K. KaushikMSc2010PhD Scholar, IOB, Bangalorebio[dot]rudra[at]gmail[dot]com
21Gadave Kaustubh SubhashJ. K. KaushikMVSc2010Serum Institute of India Pvt Ltd, Pune, Maharashtrakaustubhvet[at]gmail[dot]com
22Mata Naga RajaD. MalakarM. Sc.2011--
23Shashi AnandT K DattaM.Sc.2011Postdoctoral Fellow, Mitchell Cancer Institute, University of South Alalbama, USAshashianand15[at]gmail[dot]com
24Sohita OjhaS L GoswamiMSc2011-samaira[dot]sohita[at]gmail[dot]com
25Manoj KumarJ. K. KaushikMVSc2011Veterinary Officer, Deptt of Animal Husbandry, Govt of Bihar, Kundra, Kaimur, Biharmanoj2003vet[at]gmail[dot]com
26Nisha BaraD. MalakarM.Sc.2012-nishabara5432[at]gmail[dot]com
27Sirlapu Madhusudan RaoT K DattaM.Sc.2012Senior consultant Embryologist at Pearl Singapore Fertility centre and Research Institute, chennai., and Guest teaching faculty at Asia Pacific Institute of Embryology, Mysore.madhuvennela7[at]gmail[dot]com
28Subas Chandra JenaT K DattaM.V.Sc.2012Additional Veterinary Assistant Surgeon (AVAS), Malkangiri,Dept. of Fisheries and Animal Resources Development Dept(F&ARD), Govt Of Odishadrsubasvet[at]gmail[dot]com
29Chanukuppa VenkateshJ. K. KaushikMSc2012PhD Scholar, Mass spectrometry and proteomics lab, National Centre for Cell Science, NCCS complex, SPPU Campus, PO-411007venkatesh[dot]ch53[at]gmail[dot]com
30Mona Faraji HerissT K DattaM Sc.2013-monamonafar[at]gmail[dot]com
31Amit DubeyD. MalakarM.Sc.2013Doing Ph. D. at Canadadubeyamit786[at]gmail[dot]com
32Kaleem AhmedJ. K. KaushikMSc2013-kaleem0598[at]gmail[dot]com
33Samreen FatimaD. MalakarM.Sc.2014Completed her Ph. D. at JNU, Indiaasad[dot]samreen[at]gmail[dot]com
34Mr. Banshi NathM.K. SinghM.Sc.2014Ph.D. (Pursuing at University Laval, Quebec Canada)banshi[dot]nath[dot]1[at]gmail[dot]com
35Syed Mohd. Aamir Suhail J. K. KaushikMSc2014PhD Scholar, Regional Centre for Biotechnology, Faridabad, Haryanaaamirbkbz[at]yahoo[dot]com
36Miss. Vanya BhushanD. MalakarM. Sc.2015Doing Ph.D. at NDRI, Karnalbhushan[dot]vanya22[at]gmail[dot]com
37Mr. Anurag KumarM.K. SinghM. Tech.2015Ph.D. (Pursuing at NDRI, Karnal)anuragkumarbt[at]gmail[dot]com
38Gaurav Kumar ChaubeyT K DattaM Sc.2016Ph.D. Student, CSIR-IMTECH, Chandigarhgchaubey93[at]gmail[dot]com
39Ms. Kamlesh Kumari BajuaD. MalakarM. Sc.2016Doing Ph. D. at NDRI, Karnalkamleshafs123[at]gmail[dot]com
40Mr. Manish TiwariM.K. SinghM. Tech.2016Ph.D. (Pursuing at NDRI, Karnal)bt[dot]manish1[at]gmail[dot]com
41Madhisamita PandaRakesh KumarM.V.Sc.2016Veterinary Officer, State of Orissamadhusmita[dot]biotech24[at]gmail[dot]com
42Vibhanshu KumarJ. K. KaushikMSc2016PhD Scholar, IISER, Bhopalvibhu[dot]doctor[at]gmail[dot]com
43Mr. Avinash DwivediM.K. SinghM. Tech.2017-newavi[dot]gkp[at]gmail[dot]com
44Vinay MalikRakesh KumarM.Tech2017Residing in Shamli, UP.lifescience39[at]gmail[dot]com
45Ms. Haphidasara PyngropeJ. K. KaushikMSc2017Junior Research Fellow, Dept. of ENT, North Eastern Indira Gandhi Regional Institute of Health and Medical Sciences, Shillong, Meghalaya, 793018.haphidasara58[at]gmail[dot]com
46Diptesh DasRakesh KumarMSc2017Pursuing Ph.D. at NDRI, Karnaldipteshdas[at]outlook[dot]com
47Ms. Amina AmbareenJ. K. KaushikMTech2017-ameena_1633[at]outlook[dot]com
48Sakshi KhuranaT K DattaM Sc.2018Ph.D. Student, HAIC Integrated Mushroom Research & Development Center (lab), DCRUST,Murthalsakshi[dot]khurana92[at]gmail[dot]com
49Pratiksha DubeyT K DattaM Sc.2018Ph.D. Student, IISER, Mohali, Punjabpratiksha[dot]du[at]gmail[dot]com
50Suman TamangT K DattaM Sc.2018-sumsthinker[at]gmail[dot]com
51Apoorva SoniT K DattaM Sc.2019Junior Research Fellow, TMC-ACTREC, Navi Mumbai, Indiasoniapoorva7[at]gmail[dot]com
52Ramandeep SinghD. MalakarM. Sc.2019Completed M. Sc. at NDRI, Karnaldocrd95[at]gmail[dot]com
53Komal DagarRakesh KumarMSc2019Residing in Delhikomaldagar1605[at]gmail[dot]com
54Ms. Akansha BhattJ. K. KaushikMTech2019PhD Scholar, AIIMS, Delhiakanshajmd1[at]gmail[dot]com
55Vinay BhaskarD. MalakarM. Sc.2020Doing M. Sc. at NDRI, Karnalvinaybhaskar99[at]gmail[dot]com
56Ms. Navkiran KaurJ. K. KaushikMSc2020-navkirannavy[at]gmail[dot]com
57Ms. Jyoti YadavJ. K. KaushikMSc2020-yjyoti039[at]gmail[dot]com

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