#1
30th November 2016, 02:48 PM
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Msc Biotechnology Syllabus Mumbai University
My sister has completed B.SC Biotechnology Course in last year and this year she wants to take admission in PG Degree at Mumbai University. So she wants to see syllabus of M.SC Biotechnology Course before taking admission. So will you give link to download syllabus of M.SC Biotechnology Course?
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#2
30th November 2016, 03:10 PM
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Re: Msc Biotechnology Syllabus Mumbai University
As you are looking for syllabus of M.SC Biotechnology Course of Mumbai University, so here I am giving detailed syllabus: Mumbai University M.SC Biotechnology Syllabus Semester- I Biochemistry Unit I Proteins : Primary structure of proteins and their determination – end group analysis; cleavage of disulphide bond; separation, purification, characterization of polypeptide chain; specific peptide cleavage reactions. Secondary structure – Ramachandran plot, helical structure, beta structure; Tertiary structure- fibrous (Collagen) and globular (Myoglobin) structure. Protein stability, protein denaturation. Quaternary structure – (Haemoglobin) subunit interaction, symmetry, subunit composition determination Unit II Signal transduction Cell signalling pathways that control gene activity- TGF-Beta and activation of Smads: Regulation of TGF-Beta by negative feedback loops. Cancer and loss of TGF-Beta signalling, Unit III Lipids Lipoproteins – structure, function, disorders and dysfunction in Alzheimer’s disease. Unit IV Neurochemistry Anatomy and functions of neuron, organization of brain, neuronal pathways and systems, propagation of nerve impulse, ion conducting channels, synapses and gap junction, neurotransmitters, neurotoxins Immunochemistry Unit I Immunoglobulins Hematopoiesis, Immunoglobulin fine structure, Immunoglobulin superfamily ,Multigene organization of Ig gene, Variable region gene rearrangement, Generation of antibody diversity, Class switching among constant region. Synthesis, assembly, and secretion of immunoglobulins Unit II Complement system Activation, Regulation, Biological consequence of complement activation, Complement deficiency Unit III MHC and Regulation of immune response Cellular distribution of MHC molecule, Antigen processing and presentation – exogenous and endogenous antigen processing. Self - MHC restriction of T cells. Presentation of non-peptide antigens. Activation of B and T lymphocytes, T-cell regulation. Unit IV Cytokines Properties, receptors, antagonists, diseases, therapeutic use of cytokines Genomes and Transcriptomes Unit I Gene evolution and The human genome Human genome project, the content of human nuclear genome, tandemly repeated DNA, interspersed genome-wide repeats. Human mitochondrial genome. Genome evolution-Acquisition of New Genes (gene duplication, from other species, transposable elements), Non-coding DNA Unit II Mapping Genomes Genetic Mapping: DNA markers for genetic mapping, Physical Mapping: Restriction Mapping, Fluorescent in situ hybridization (FISH), Sequence tagged site (STS) mapping. Unit III Transcription Initiation in prokaryotes and eukaryotes DNA-Protein interactions during Transcription Initiation, Regulation of Transcription initiation. Unit IV Synthesis and Processing of RNA Synthesis of eukaryotic mRNAs by RNA polymerase II, Intron splicing. Synthesis and processing of Non-coding RNAs: Transcript elongation and termination by RNA polymerases I and III, Introns in eukaryotic pre-rRNA and pre-tRNA. Processing of Pre-RNA. Degradation of mRNAs Biophysics Unit I DNA Topology Different forms of DNA, - A/B/C/Z and RL form of double helical DNA, Triple Helix, Nucleic acid binding protein – Leucine Zipper, Zinc fingers, OB fold, Beta Barrel, Helix-turn-helix, Helix-loophelix. Linking number, Supercoiling, Topoisomerases. Unit II Protein secondary structure Protein folding. The different pathways of protein folding and its co-relation with protein stability. Molecular chaperons Unit III Advances in Microscopy Different versions of electron microscopy, Confocal Microscopy Unit IV Membrane mimicry Liposome structure and their uses in drug targeting. solubilisation of the membrane by using different detergents. Membrane mimicry. |
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