NTHRYS provides Molecular Biology Research Training for interested candidates at its Hyderabad facility, Telangana. Please refer below for more details including Fee strctures, Eligibility, Protocols and Modules etc.,. Please do call / message / whatsapp for more details on 9014935156 [India - +91]
Eligibility: BSc / BTech / MSc / MTech / MPhil / PhD in any Life Sciences studying or completed students
A technique used to investigate the interaction between proteins and DNA in the cell.
Used to study gene expression by attaching a reporter gene to a regulatory sequence of interest and measuring its activity.
A method for measuring the quantity of a target DNA sequence in real-time by amplification.
Used to detect specific proteins in a sample based on their size and antibody binding.
Enables rapid sequencing of large stretches of DNA base pairs spanning entire genomes.
A powerful tool for editing genomes with high precision by creating double-strand breaks at targeted locations.
A method to silence gene expression in cells by using small RNA molecules to degrade mRNA of a specific gene.
A cytogenetic technique that uses fluorescent probes to detect and localize the presence of specific DNA sequences on chromosomes.
Analyzes proteins by measuring the mass of peptides and their fragments to identify and quantify proteins in a sample.
Used to examine the gene expression profiles of individual cells for comprehensive analysis.
Detects DNA-binding proteins by observing the mobility shift of a DNA-protein complex during electrophoresis.
Measures binding interactions between molecules, such as protein-protein or protein-DNA interactions, in real-time without labeling.
A molecular biology method used to discover protein-protein interactions by testing for physical interactions between two proteins.
Introduces specific, predetermined mutations into a DNA sequence to study the effects of those mutations.
The process of introducing foreign DNA into bacteria, enabling the bacteria to express new genetic information.
Similar to bacterial transformation but used to introduce DNA into yeast cells for genetic studies.
A technique used to separate DNA or RNA fragments based on their size and charge by applying an electric field.
A tool for analyzing gene expression or for genotyping multiple regions of a genome simultaneously.
A plate-based assay technique designed for detecting and quantifying soluble substances such as peptides, proteins, antibodies, and hormones.
Techniques used to maintain and grow cell lines or tissues in culture media under controlled conditions.
A process used to separate cellular components while preserving individual functions of each component.
A technique that uses fluorescent-labeled antibodies to detect specific antigens in cells.
The introduction of nucleic acids into cells to produce genetically modified cells.
A method for delivering genetic material into cells using lentiviruses as vectors.
Used to isolate a specific protein from a solution by using an antibody that specifically binds to that protein.
A technology that is used to analyze the physical and chemical characteristics of particles in a fluid as it passes through at least one laser.
Converts RNA to DNA with reverse transcriptase and then amplifies specific DNA targets using PCR.
A method for detecting antigens in cells of a tissue section by exploiting the principle of antibodies binding specifically to antigens in biological tissues.
A tool to study how many genes are activated in different cell samples, which helps in understanding gene expression patterns.
Various methods used to isolate a single type of protein from a complex mixture, which is crucial for studying protein structure and function.
Used to determine the pattern of methylation of DNA by treating DNA with bisulfite and then sequencing it.
A technique that involves the transfer of RNA from a gel to a membrane and its subsequent detection by hybridization with a labeled probe.
Similar to Northern blotting but for DNA. It detects specific DNA sequences within a DNA sample.
Combines chromatin immunoprecipitation with DNA sequencing to identify the binding sites of DNA-associated proteins.
The process of preparing DNA or RNA for sequencing, which includes fragmenting the genetic material, adding adapters, and sometimes amplification.
A technique to introduce DNA, RNA, or proteins into cells using an electric pulse that temporarily opens the cell membranes.
A method where an organism is engineered to carry genes that have been made inoperative (have been "knocked out" of the genome).
The regulation of gene expression in a cell to prevent the expression of a certain gene.
Expressing protein in a host system and then purifying it from other cellular components for further study.
The synthesis of RNA from a DNA template by RNA polymerase under laboratory conditions, outside living cells.
The process of joining two strands of DNA molecules by a covalent bond, typically catalyzed by DNA ligase.
A method to determine the atomic and molecular structure of a crystal by diffracting X-ray beams through the crystal.
The process of purifying nucleic acids (DNA or RNA) from biological samples.
A technique that provides a snapshot of which mRNAs are being actively translated into proteins by capturing and sequencing fragments of mRNAs protected by ribosomes.
Injecting a substance into a microscopic structure, such as a single cell or a nucleus.
A method to deliver genetic material into cells by encapsulating it in liposomes which fuse with the cell membrane.
The process of forming a protein crystal, which can then be used for structural biology studies, particularly X-ray crystallography.
A technique in analytical chemistry used to separate, identify, and quantify components in a mixture.
Methods used to study the activity of enzymes, allowing the understanding of enzyme kinetics and function.
Techniques used to analyze the structure and function of glycans (sugar chains or oligosaccharides) attached to proteins and lipids.
A technique used to obtain the full-length sequence of an RNA transcript.
A genetic method that looks for patterns of inheritance of genetic markers in large families to discover the location of disease-causing genes.
A laboratory technique used to study protein-protein, protein-peptide, and protein-DNA interactions by using bacteriophages to connect proteins with the genetic information that encodes them.
A form of light absorption spectroscopy that measures the difference in absorbance of right-handed and left-handed circularly polarized light, which can be indicative of the conformation of biological molecules.
Utilizing software tools to gather, analyze, and represent data from biological research, particularly useful in genomics and proteomics.
A set of experimental methods used to assemble recombinant DNA molecules and to direct their replication within host organisms.
A technique used to detect biomolecules, which is simpler and faster than Western blotting because it does not involve separation by electrophoresis.
The process of generating antibodies specific to an antigen, followed by the purification of these antibodies for further experimental use.
A method for measuring DNA strand breaks in individual cells to assess DNA damage and repair.
A method to study protein structure and interactions by observing how proteins affect the reactivity of nearby molecules.
A variant of immunoprecipitation used to isolate proteins and their interacting partners from a cell lysate.
The chemical synthesis of peptides, which are short chains of amino acid monomers linked by peptide bonds.
A technique that separates ions based on their electrophoretic mobility with the use of an applied voltage.
The study of genetic material recovered directly from environmental samples, providing insights into the microbial communities and their natural processes.
The study of the three-dimensional structures of every protein encoded by a given genome.
A method of measuring variations of single nucleotide polymorphisms between members of a species to understand genetic makeup.
A technique used in quantitative proteomics by incorporating non-radioactive isotopes into proteins or other biomolecules.
Techniques such as siRNA or shRNA that reduce the expression of specific genes in cells to study their function.
A type of scanning probe microscopy with a resolution on the order of fractions of a nanometer, more than 1000 times better than the optical diffraction limit.
The process of reverting mature, specialized cells into induced pluripotent stem cells.
The use of time-lapse microscopy to study living cells over time, which can provide insight into cellular function and behavior.
Methods to measure protease activity in a sample to study various biological processes and disease states.
A method to study the binding interaction between proteins and nucleic acids by pulling down the complex from a mixture.
A technique used to assess the stability of proteins and their complexes with ligands by monitoring protein denaturation through temperature increases.
A method to measure the size distribution and structure of molecules and complexes in solution by detecting scattered light.
A technique to measure the heat released or absorbed during a biochemical binding event, providing insights into the thermodynamics of the interaction.
An advanced version of SPR for detailed imaging and analysis of biomolecular interactions.
An electrophoretic technique used to analyze protein complexes in their native states.
A high-throughput antibody-based technique used for protein detection and quantitation in a complex biological sample.
A method to identify oligonucleotides that bind to a specific target molecule with high affinity.
Used to measure the movement of molecules within live cells by observing the recovery of fluorescence after a bleaching event.
A technique that measures the decay rate of fluorescence from a sample, providing insights into dynamic interactions at the molecular level.
Methods to assess the ability of cells to move through an environment, important for studying cancer metastasis and other processes.
A versatile assay technique used for detecting biomolecular interactions in a homogeneous format.
A technique that measures the heat flow associated with phase transitions in materials as a function of temperature, useful in studying protein folding/unfolding.
A method to study DNA-protein interaction by detecting the protection of DNA from nucleolytic cleavage by bound proteins.
A scientific instrument that uses a highly focused laser beam to manipulate microscopic particles including cells and molecules.
A technique to detect proteins, protein interactions, and modifications with very high sensitivity and specificity.
A method for transferring genetic material between bacterial cells through direct cell-to-cell contact.
Techniques to introduce new genes into animals to study gene function and disease processes.
Used to measure the distance and interaction between two light-sensitive molecules.
Methods to study the ion channels in cells by recording the current flow in very small patches of the cell membrane.
Technologies that process or manipulate small amounts of fluids using channels with dimensions of tens of micrometers.
A digital molecular barcoding technology for profiling various types of molecules from RNA to DNA and proteins.
A technique to selectively isolate specific cells from a heterogeneous tissue section via direct microscopic visualization.
Techniques like FACS or magnetic sorting used to separate cells based on their properties for further analysis or culture.
Used to study the proximity between different protein regions or proteins in a complex by stabilizing their interactions with chemical links.
A form of electron microscopy where samples are studied at cryogenic temperatures, allowing the observation of structures in their native environment.
A basic form of PCR used to amplify DNA to detectable levels, followed by analysis via gel electrophoresis or other methods.
A highly precise approach to quantitative PCR that partitions the sample into many individual reactions.
A technique to analyze biomolecules by observing their movement through temperature gradients.
A method to produce large numbers of identical antibodies (monoclonal antibodies).
A method to identify RNA-binding proteins by capturing them with a bait RNA.
The artificial synthesis of double-stranded DNA molecules without a template.
A method to detect protein-protein interactions by exploiting the properties of yeast genetics.
Similar to Western blotting but used to detect protein-protein interactions specifically.
A technique to study changes in gene expression caused by epigenetic modifications, such as DNA methylation and histone modification.
Used for the characterization of small particles in solution by measuring the scattering of a laser beam.
A technique that visualizes the spatial distribution of compounds by their mass-to-charge ratios.
The study of how drugs are absorbed, distributed, metabolized, and excreted in living organisms.
Studying the developmental processes in zebrafish to understand vertebrate development and genetic diseases.
Techniques to reprogram somatic cells to a pluripotent state that can give rise to any cell type.
A method to analyze the spatial organization of chromatin in a cell.
The study of the rates of enzyme-catalyzed reactions and how they are affected by various conditions and inhibitors.
A technique to detect DNA methylation patterns within specific DNA regions.
Combines ChIP with microarray technology to identify the binding sites of DNA-associated proteins across the genome.
Techniques involving antisense oligonucleotides to interfere with the expression of specific genes.
The use of robotic systems to perform rapid DNA sequencing.
Techniques to determine the number of viable cells in a sample based on certain biochemical criteria.
The study of the metabolic processes within cells that drive energy production.
The large-scale study of proteomes, including the set of expressed proteins in a cell, tissue, or organism, at certain times.
Note: NTHRYS currently operates through three registered entities: NTHRYS BIOTECH LABS (NBL), NTHRYS OPC PVT LTD (NOPC), and NTHRYS Project Greenshield (NPGS).