In this slide contains principle, types, methods and application of Western Blotting Technique.
Presented by: T.NIRANJAN REDDY (Department of pharmacology).
RIPER, anantapur
The western blot is a technique used to detect specific proteins in a sample. It involves separating proteins by size using gel electrophoresis, transferring them to a membrane, and using antibodies to detect the target protein. The key steps are sample preparation, gel electrophoresis, blotting, blocking, antibody probing, and detection. Western blotting allows researchers to identify proteins from complex mixtures and is widely used in molecular biology and medical diagnosis, such as detecting HIV, HBV, and HSV infections.
Western blotting is a technique used to detect specific proteins in a tissue sample. It involves separating proteins by gel electrophoresis based on size, transferring them to a membrane, and using antibodies to identify a target protein. The process starts with preparing the tissue sample, separating proteins by SDS-PAGE gel electrophoresis, transferring proteins to a membrane, blocking the membrane to reduce nonspecific antibody binding, probing with primary and secondary antibodies, washing unbound antibodies, and detecting the target protein. Western blotting is useful for applications like diagnosing diseases and studying gene expression.
This document provides an overview of mutagenesis techniques including: types of mutagenesis like site-directed mutagenesis; applications in molecular biology research and protein engineering; methods for screening mutants like visual screening; and advantages and future prospects of mutation breeding like using TILLING to detect single nucleotide mutations.
Western blotting is a technique used to detect specific proteins in a sample. It involves transferring proteins separated by gel electrophoresis to a membrane and using antibodies to identify the target protein. The key steps are sample preparation, gel electrophoresis, protein transfer, blocking, washing, and detection of the target protein. Western blotting is widely used in research and clinical diagnosis due to its ability to identify proteins with high sensitivity and specificity.
This document discusses restriction enzymes, including their discovery, types, subunits, nomenclature, recognition sequences, properties, and applications. Restriction enzymes are bacterial enzymes that cut DNA at specific recognition sequences. There are three main types - Type I cut DNA randomly, Type II cut within or near their recognition sequences, and Type III cut nearby. They are used in gene cloning, protein expression, DNA manipulation, and studying DNA sequences.
Recombinant DNA technology involves combining DNA sequences from different species that would not normally occur together to create artificial DNA and alter the genetics of living cells. There are three main methods to create recombinant DNA - transformation, phage introduction, and non-bacterial transformation. Transformation involves selecting a DNA fragment, inserting it into a vector, and introducing the vector into a host cell like E. coli. Recombinant DNA technology has many applications, including producing proteins and hormones, disease diagnosis and treatment, genetically engineering plants, and forensic analysis.
Polymerase chain reaction (PCR) is used to amplify a specific segment of DNA. It involves repeated cycles of denaturing DNA into single strands, annealing primers to the strands, and extending the primers to synthesize new strands. This results in exponential amplification of the target DNA sequence. PCR requires a DNA template, primers, DNA polymerase, nucleotides, and repeated temperature changes for denaturation, annealing and extension. Each cycle approximately doubles the amount of target DNA.
Restriction Endonucleases are enzymes from bacteria that can recognize specific base sequences in DNA and cut (restrict) the DNA at that site (the restriction site). This powerpoint sllides illustrate the introduction, examples, nomenclature and types of restriction endonucleases.
Hybridoma technology is a method for producing large number of identical antibodies called monoclonal antibodies.
It was discovered by G.kohler and C.milstein in 1975. they were awarded nobel prize for physiology and medicine in 1975.
The hybrid cells are produced by fusing B- lumphocyte with myeloma cells or tumour cells.
The B-lymphocyte have the ability to produce large number of antibodies and tumour cells have indefinite growth.
This is why two cells are used for the production of hybrid cell
Western blotting is a technique used to detect specific proteins in a sample. It involves separating proteins by electrophoresis, transferring them to a membrane, and using antibodies to identify a target protein. There are several key steps: extraction of proteins from a sample, separation by size using gel electrophoresis, transferring proteins from the gel to a membrane, blocking the membrane to prevent nonspecific antibody binding, incubation with primary and secondary antibodies to detect the target protein, and use of a substrate to visualize the antibody-protein complex. Western blotting has applications in disease diagnosis, detecting defective proteins, and confirming the presence of viruses or bacteria.
Southern blotting is a technique used to detect specific DNA sequences. It involves extracting DNA from cells, cutting the DNA with restriction enzymes, separating fragments via electrophoresis, transferring DNA to a membrane, then using a labeled probe to hybridize and identify the target sequence via autoradiography. Southern blotting allows identification of mutations, deletions and rearrangements, and is used for cancer prognosis, genetic disease diagnosis, DNA fingerprinting and more. It is an effective detection method but is also complex, labor-intensive, and time-consuming.
Southern blotting is a technique used to detect specific DNA sequences in a DNA sample. It involves separating DNA fragments by size via gel electrophoresis, transferring them to a membrane, and using a labeled probe to identify the DNA fragment of interest through hybridization and autoradiography. Key steps include restriction enzyme digestion of DNA, gel electrophoresis, transferring fragments to a membrane, hybridizing with a probe, washing unbound probe, and detecting the bound probe fragment. This allows researchers to identify specific DNA sequences and analyze DNA samples.
This document summarizes several blotting techniques used in molecular biology to detect biomolecules like DNA, RNA, and proteins. Southern blotting detects specific DNA sequences, Northern blotting detects RNA, and Western blotting detects proteins. Eastern blotting detects post-translational modifications to proteins. Dot blotting directly applies biomolecule samples to a membrane as dots to detect presence or absence without separation by size. These techniques involve transferring molecules to a membrane, probing with a labeled probe, washing, and detecting hybridized probes.
Blotting technique including Southern , Northern and Western blotting Rohit Mondal
he given ppt contains all the blotting techniques which is being studied by students in Biotechnology related subject and this PPT contais all blotting techniques in a very elaborative concise manner includes procedure principle application etc so which itwould help any bio student to take proper knowledge in this topic. I hope you will enjoy the content of the topic and would be able to grasp the topic properly
The document discusses the production of recombinant human insulin from bacteria. It describes how insulin is normally produced in the pancreas and its functions. It then explains that E. coli cannot properly produce insulin due to its inability to cleave proinsulin's C-peptide chain. The process used involves fusing the human insulin A and B chain genes separately to bacterial genes, expressing each chain in E. coli, then combining and refolding the purified chains to form active insulin. This recombinant technique allows for large-scale commercial production of human insulin for diabetes treatment.
Western blotting is a technique used to detect specific proteins in a sample. It involves separating proteins by gel electrophoresis, transferring them to a membrane, and using antibodies to identify target proteins. The key steps are tissue preparation, gel electrophoresis, protein transfer to a membrane, blocking of the membrane to prevent nonspecific antibody binding, incubation with primary and secondary antibodies, and detection of bound antibodies through methods like colorimetric reactions or chemiluminescence. Western blotting has applications in detecting conditions like HIV and hepatitis B. While sensitive, it takes longer than other tests and may be more costly.
Gel filtration chromatography separates molecules according to size by passing a liquid mobile phase containing the molecules through a column packed with porous beads. Larger molecules are excluded from the pores and elute earlier, while smaller molecules can enter the pores and are retained longer in the column before eluting. It is commonly used to purify and determine the molecular weights of proteins, polymers, and other biomolecules.
DNA ligase is an enzyme that catalyzes the formation of phosphodiester bonds between DNA fragments, joining two DNA strands together. It plays an important role in DNA replication by joining Okazaki fragments and filling in gaps, as well as in DNA repair and genetic engineering techniques like cloning. The most commonly used DNA ligase is from bacteriophage T4, which utilizes ATP as a cofactor and works efficiently at lower temperatures to ligate DNA strands with either sticky or blunt ends.
Polymerase Chain Reaction, PCR-139, Definition, Principle, Types and applicat...someshwar mankar
PCR is a technique used to amplify specific DNA sequences. It involves denaturing DNA into single strands, annealing primers to the strands, and extending the primers to synthesize new strands. This process is repeated for many cycles, exponentially amplifying the target DNA sequence. PCR has many applications including disease diagnosis, genetic fingerprinting, detection of genetic mutations, and forensic analysis. It provides a sensitive and specific way to detect and analyze DNA.
Reverse transcription polymerase chain reaction (RT-PCR) is a technique used to detect RNA expression and qualitatively detect gene expression by creating cDNA from RNA. RT-PCR involves reverse transcribing RNA into cDNA using reverse transcriptase, then amplifying the cDNA using PCR. It can be performed as a one-step or two-step process. RT-PCR is commonly used in research, genetic disease diagnosis, cancer detection, and studying viruses with RNA genomes.
This document discusses various gene sequencing methods. It begins by introducing DNA and the importance of sequencing the genetic code. It then describes several early sequencing techniques like Sanger sequencing using chain termination or chemical cleavage. It discusses the need for sequencing to understand genetic conditions. The document also covers topics like genome sequencing, genomics, and high-throughput sequencing techniques like dye-terminator sequencing which replaced radioactive labels with fluorescent labels to automate the process.
Objectives:
After the end of the presentation we’ll know -
What is cloning vector?
Why cloning vector?
History
Features of a cloning vector
Types of cloning vector
Plasmid
Bacteriophage
Cosmid
Bacterial Artificial Chromosome (BAC)
Yeast Artificial Chromosome (BAC)
Human Artificial Chromosome (HAC)
Retroviral Vectors
What determines choice of vector?
Vector in molecular gene cloning
Cloning vector - The molecular analysis of DNA has been made possible by the cloning of DNA. The two molecules that are required for cloning are the DNA to be cloned and a cloning vector.
A cloning vector is a small piece of DNA taken from a virus, a plasmid or the cell of a higher organism, that can be stably maintained in an organism and into which a foreign DNA fragment can be inserted for cloning purposes.
Most vectors are genetically engineered.
The cloning vector is chosen according to the size and type of DNA to be cloned.
The vector therefore contains features that allow for the convenient insertion or removal of DNA fragment in or out of the vector, for example by treating the vector and the foreign DNA with a restriction enzyme and then ligating the fragments together.
After a DNA fragment has been cloned into a cloning vector, it may be further subcloned into another vector designed for more specific use.
This document discusses the history and various methods of DNA sequencing. It begins with a brief overview of DNA sequencing and its uses. It then outlines some of the major developments in DNA sequencing techniques, including the earliest RNA sequencing in 1972, Sanger sequencing in 1977, and the first complete genome of Haemophilus influenzae in 1995. The document proceeds to provide more detailed explanations of several DNA sequencing methods, such as Sanger sequencing, pyrosequencing, shotgun sequencing, Illumina sequencing, and SOLiD sequencing.
This document summarizes antigen processing and presentation. It discusses that antigen presenting cells such as macrophages, dendritic cells, and B cells express class II MHC molecules and provide co-stimulatory signals to activate T helper cells. These cells internalize antigens through phagocytosis or endocytosis, degrade them into peptides, and present the peptides bound to class II MHC on their surface. The document also describes the major histocompatibility complex and the roles of class I and class II MHC molecules in antigen presentation to T cells. It outlines the exogenous and endogenous antigen processing pathways, how exogenous antigens are presented by class II MHC and endogenous antigens by class I MHC.
Gene sequencing is the technique that determines the order of nucleotide bases in DNA. It allows researchers to read genetic information and understand genes. The first genome sequenced was a bacteriophage in 1977. Techniques have advanced from Sanger sequencing to second-generation sequencing using platforms like Illumina and third-generation single-molecule techniques. Gene sequencing has various applications in medicine, forensics, agriculture, cancer research and more. It is an important tool for understanding genomes and their relationship to traits and disease.
Introduction to Analytical Techniques in Phaese III,
Spectrophotometry, Reflectance photometry, Nephelometry & Turbidimetry, Osmometry, Potentiometry, Flowcytometry, Densitometry, Electrophoresis, LC-MS, ICP-MS
Presented by
B. Kranthi Kumar
Department of Pharmacology
In this slide contains analytical techniques in phase-3 clinical trials.
Presented by: KRANTHI KUMAR BONALA (Department of pharmacology).
RIPER, anantapur
Hybridoma technology is a method for producing large number of identical antibodies called monoclonal antibodies.
It was discovered by G.kohler and C.milstein in 1975. they were awarded nobel prize for physiology and medicine in 1975.
The hybrid cells are produced by fusing B- lumphocyte with myeloma cells or tumour cells.
The B-lymphocyte have the ability to produce large number of antibodies and tumour cells have indefinite growth.
This is why two cells are used for the production of hybrid cell
Western blotting is a technique used to detect specific proteins in a sample. It involves separating proteins by electrophoresis, transferring them to a membrane, and using antibodies to identify a target protein. There are several key steps: extraction of proteins from a sample, separation by size using gel electrophoresis, transferring proteins from the gel to a membrane, blocking the membrane to prevent nonspecific antibody binding, incubation with primary and secondary antibodies to detect the target protein, and use of a substrate to visualize the antibody-protein complex. Western blotting has applications in disease diagnosis, detecting defective proteins, and confirming the presence of viruses or bacteria.
Southern blotting is a technique used to detect specific DNA sequences. It involves extracting DNA from cells, cutting the DNA with restriction enzymes, separating fragments via electrophoresis, transferring DNA to a membrane, then using a labeled probe to hybridize and identify the target sequence via autoradiography. Southern blotting allows identification of mutations, deletions and rearrangements, and is used for cancer prognosis, genetic disease diagnosis, DNA fingerprinting and more. It is an effective detection method but is also complex, labor-intensive, and time-consuming.
Southern blotting is a technique used to detect specific DNA sequences in a DNA sample. It involves separating DNA fragments by size via gel electrophoresis, transferring them to a membrane, and using a labeled probe to identify the DNA fragment of interest through hybridization and autoradiography. Key steps include restriction enzyme digestion of DNA, gel electrophoresis, transferring fragments to a membrane, hybridizing with a probe, washing unbound probe, and detecting the bound probe fragment. This allows researchers to identify specific DNA sequences and analyze DNA samples.
This document summarizes several blotting techniques used in molecular biology to detect biomolecules like DNA, RNA, and proteins. Southern blotting detects specific DNA sequences, Northern blotting detects RNA, and Western blotting detects proteins. Eastern blotting detects post-translational modifications to proteins. Dot blotting directly applies biomolecule samples to a membrane as dots to detect presence or absence without separation by size. These techniques involve transferring molecules to a membrane, probing with a labeled probe, washing, and detecting hybridized probes.
Blotting technique including Southern , Northern and Western blotting Rohit Mondal
he given ppt contains all the blotting techniques which is being studied by students in Biotechnology related subject and this PPT contais all blotting techniques in a very elaborative concise manner includes procedure principle application etc so which itwould help any bio student to take proper knowledge in this topic. I hope you will enjoy the content of the topic and would be able to grasp the topic properly
The document discusses the production of recombinant human insulin from bacteria. It describes how insulin is normally produced in the pancreas and its functions. It then explains that E. coli cannot properly produce insulin due to its inability to cleave proinsulin's C-peptide chain. The process used involves fusing the human insulin A and B chain genes separately to bacterial genes, expressing each chain in E. coli, then combining and refolding the purified chains to form active insulin. This recombinant technique allows for large-scale commercial production of human insulin for diabetes treatment.
Western blotting is a technique used to detect specific proteins in a sample. It involves separating proteins by gel electrophoresis, transferring them to a membrane, and using antibodies to identify target proteins. The key steps are tissue preparation, gel electrophoresis, protein transfer to a membrane, blocking of the membrane to prevent nonspecific antibody binding, incubation with primary and secondary antibodies, and detection of bound antibodies through methods like colorimetric reactions or chemiluminescence. Western blotting has applications in detecting conditions like HIV and hepatitis B. While sensitive, it takes longer than other tests and may be more costly.
Gel filtration chromatography separates molecules according to size by passing a liquid mobile phase containing the molecules through a column packed with porous beads. Larger molecules are excluded from the pores and elute earlier, while smaller molecules can enter the pores and are retained longer in the column before eluting. It is commonly used to purify and determine the molecular weights of proteins, polymers, and other biomolecules.
DNA ligase is an enzyme that catalyzes the formation of phosphodiester bonds between DNA fragments, joining two DNA strands together. It plays an important role in DNA replication by joining Okazaki fragments and filling in gaps, as well as in DNA repair and genetic engineering techniques like cloning. The most commonly used DNA ligase is from bacteriophage T4, which utilizes ATP as a cofactor and works efficiently at lower temperatures to ligate DNA strands with either sticky or blunt ends.
Polymerase Chain Reaction, PCR-139, Definition, Principle, Types and applicat...someshwar mankar
PCR is a technique used to amplify specific DNA sequences. It involves denaturing DNA into single strands, annealing primers to the strands, and extending the primers to synthesize new strands. This process is repeated for many cycles, exponentially amplifying the target DNA sequence. PCR has many applications including disease diagnosis, genetic fingerprinting, detection of genetic mutations, and forensic analysis. It provides a sensitive and specific way to detect and analyze DNA.
Reverse transcription polymerase chain reaction (RT-PCR) is a technique used to detect RNA expression and qualitatively detect gene expression by creating cDNA from RNA. RT-PCR involves reverse transcribing RNA into cDNA using reverse transcriptase, then amplifying the cDNA using PCR. It can be performed as a one-step or two-step process. RT-PCR is commonly used in research, genetic disease diagnosis, cancer detection, and studying viruses with RNA genomes.
This document discusses various gene sequencing methods. It begins by introducing DNA and the importance of sequencing the genetic code. It then describes several early sequencing techniques like Sanger sequencing using chain termination or chemical cleavage. It discusses the need for sequencing to understand genetic conditions. The document also covers topics like genome sequencing, genomics, and high-throughput sequencing techniques like dye-terminator sequencing which replaced radioactive labels with fluorescent labels to automate the process.
Objectives:
After the end of the presentation we’ll know -
What is cloning vector?
Why cloning vector?
History
Features of a cloning vector
Types of cloning vector
Plasmid
Bacteriophage
Cosmid
Bacterial Artificial Chromosome (BAC)
Yeast Artificial Chromosome (BAC)
Human Artificial Chromosome (HAC)
Retroviral Vectors
What determines choice of vector?
Vector in molecular gene cloning
Cloning vector - The molecular analysis of DNA has been made possible by the cloning of DNA. The two molecules that are required for cloning are the DNA to be cloned and a cloning vector.
A cloning vector is a small piece of DNA taken from a virus, a plasmid or the cell of a higher organism, that can be stably maintained in an organism and into which a foreign DNA fragment can be inserted for cloning purposes.
Most vectors are genetically engineered.
The cloning vector is chosen according to the size and type of DNA to be cloned.
The vector therefore contains features that allow for the convenient insertion or removal of DNA fragment in or out of the vector, for example by treating the vector and the foreign DNA with a restriction enzyme and then ligating the fragments together.
After a DNA fragment has been cloned into a cloning vector, it may be further subcloned into another vector designed for more specific use.
This document discusses the history and various methods of DNA sequencing. It begins with a brief overview of DNA sequencing and its uses. It then outlines some of the major developments in DNA sequencing techniques, including the earliest RNA sequencing in 1972, Sanger sequencing in 1977, and the first complete genome of Haemophilus influenzae in 1995. The document proceeds to provide more detailed explanations of several DNA sequencing methods, such as Sanger sequencing, pyrosequencing, shotgun sequencing, Illumina sequencing, and SOLiD sequencing.
This document summarizes antigen processing and presentation. It discusses that antigen presenting cells such as macrophages, dendritic cells, and B cells express class II MHC molecules and provide co-stimulatory signals to activate T helper cells. These cells internalize antigens through phagocytosis or endocytosis, degrade them into peptides, and present the peptides bound to class II MHC on their surface. The document also describes the major histocompatibility complex and the roles of class I and class II MHC molecules in antigen presentation to T cells. It outlines the exogenous and endogenous antigen processing pathways, how exogenous antigens are presented by class II MHC and endogenous antigens by class I MHC.
Gene sequencing is the technique that determines the order of nucleotide bases in DNA. It allows researchers to read genetic information and understand genes. The first genome sequenced was a bacteriophage in 1977. Techniques have advanced from Sanger sequencing to second-generation sequencing using platforms like Illumina and third-generation single-molecule techniques. Gene sequencing has various applications in medicine, forensics, agriculture, cancer research and more. It is an important tool for understanding genomes and their relationship to traits and disease.
Introduction to Analytical Techniques in Phaese III,
Spectrophotometry, Reflectance photometry, Nephelometry & Turbidimetry, Osmometry, Potentiometry, Flowcytometry, Densitometry, Electrophoresis, LC-MS, ICP-MS
Presented by
B. Kranthi Kumar
Department of Pharmacology
In this slide contains analytical techniques in phase-3 clinical trials.
Presented by: KRANTHI KUMAR BONALA (Department of pharmacology).
RIPER, anantapur
Target Validation
Introduction,Drug discovery, Target identification and validation, Target validation and techniques
By
Ms. B. Mary Vishali
Department of Pharmacology
In this slide contains introduction, methods, supporting media for zone electrophoresis.
Presented by: Mary Vishali. (Department of pharmacology),
RIPER, anantapur.
In this slide contains introduction, principle, types, equipment's and applications of Enzyme linked immunosorbent assay.
Presented by: D.Sudheer Reddy. (Department of pharmacology)
RIPER, anantapur.
In this slide contains introduction, principle, methods, factors, application and disadvantage of Horizontal Electrophoresis.
Presented by: A.Geethanjali (Department of pharmacology),
RIPER, anantapur.
This document discusses vertical gel electrophoresis. It begins with an introduction explaining that gel electrophoresis separates macromolecules like DNA, RNA, and proteins based on size and charge. It then describes the principles of vertical gel electrophoresis, different types of polyacrylamide gel electrophoresis (PAGE), and two-dimensional PAGE. Applications include estimating molecular weights, identifying protein subunits, and purification. Advantages are stable gels and good resolution of small molecules, while disadvantages include more difficult preparation than agarose gels.
Introduction to Screening Models Of Anti Cancer Drugs
Need for novel anti cancer drugs, In - vitro methods, In - vivo methods, Advantages and disadvantages
Presented by
T. Niranjan Reddy
Department of Pharmacology
In this slide contains the deep explanation of Methods of Determination for Drug-Excipient Compatibility Studies.
Presented by: G.Aravind Kumar (Department of industrial pharmacy),
RIPER, anantapur.
In this slide contains introduction, principle, precautions, solution and assay method for vitamin B series.
Presented by: P. VENKATESH (Department of pharmaceutical analysis),
RIPER, anantapur
In this slide contains Introduction about XRD and there interpretation.
Presented by: Mohumed omar Mahmoud. (Department of pharmaceutics).
RIPER, anantapur.
Introduction to Applications of Proteomics Science,
Proteomics- Techniques, Applications of proteomics
Presented by
A. Harsha Vardhan Naidu
Department of Pharmacology
In this slide contains principle working of XRD and there applications.
Presented by: J Lokdeep Reddy. (Department of pharmaceutics),
RIPER, anantapur.
Introduction to Analytical Methods In Invitro Techniques, Analytical Methods, In Vitro Techniques, Spectroscopic Techniques, Chromatography, Electrochemical methods, ELISA, RIA, Bioassay, Electrophoresis
Presented by
K. Thanmaya Divya
Department of Pharmacology
In this slide contains introduction, principle and applications of differential scanning colorimetry.
Presented by: G.Kavya (Department of pharmaceutics)
RIPER,anantapur.
The document describes the development of a new magnetic solid phase extraction (MSPE) adsorbent called polyDOPA@Ag-MNPs for the analysis of trace beta-blockers in biological samples. PolyDOPA@Ag-MNPs were synthesized by reducing silver ions on the surface of magnetic nanoparticles coated with poly(3,4-dihydroxyphenylalanine). The adsorbent was able to isolate beta-blockers from sample matrices using a magnetic field. Optimization of the MSPE method identified pH 7, 2 minutes adsorption time, 4 mg polyDOPA@Ag-MNPs, methanol containing 1% acetic acid as the eluent, 2 minutes elution
JOURNAL CLUB PRESENTATION (20L81S0402-PA & QA)
Presented by: K VENKATSAI PRASAD (Department of pharmaceutical analysis and quality assurance).RIPER, anantapur
The document discusses the qualification of high performance thin layer chromatography (HPTLC). It describes the four types of qualification: design qualification, installation qualification, operation qualification, and performance qualification. Design qualification verifies specifications and review methods. Installation qualification documents compliance at installation. Operation qualification documents consistent performance within operating ranges. Performance qualification ascertains the instrument is suitable for specific analytical tasks. The document then provides examples of tests to check HPTLC performance, including linearity of spotting, reproducibility of spotting, and detection capacity.
Effects of various chemical factors on in-vitro growth of tissue culture. Various factors like Environmental, Chemical, Physical, and photoperiod affect plant tissue in vitro growth. Slide discuss about the chemical factors like Macronutrients, micronutrients, PGR as well include the new chemical factor that are descovered recently like Meta-topolin, TDZ etc.
The Arctic through the lens of data visualizationZachary Labe
26 February 2025…
Rider University, Global Biogeochemistry Class Visit (Presentation): Arctic climate change through the lens of data visualization, NOAA GFDL, Princeton, USA.
Hormones and the Endocrine System | IGCSE BiologyBlessing Ndazie
This IGCSE Biology presentation explores hormones and the endocrine system, explaining their role in controlling body functions. Learn about the differences between nervous and hormonal control, major endocrine glands, key hormones (such as insulin, adrenaline, and testosterone), and homeostasis. Understand how hormones regulate growth, metabolism, reproduction, and the fight-or-flight response. A perfect resource for Cambridge IGCSE students preparing for exams!
Variation and Natural Selection | IGCSE BiologyBlessing Ndazie
This extensive slide deck provides a detailed exploration of variation and natural selection for IGCSE Biology. It covers key concepts such as genetic and environmental variation, types of variation (continuous and discontinuous), mutation, evolution, and the principles of natural selection. The presentation also explains Darwin’s theory of evolution, adaptation, survival of the fittest, selective breeding, antibiotic resistance in bacteria, and speciation. With illustrative diagrams, real-life examples, and exam-style questions, this resource is ideal for IGCSE students, teachers, and independent learners preparing for exams.
Coordination and Response: The Nervous System | IGCSE BiologyBlessing Ndazie
This comprehensive IGCSE Biology presentation explains the nervous system, focusing on how the body coordinates and responds to stimuli. Learn about the central and peripheral nervous systems, reflex actions, neurons, synapses, and the role of neurotransmitters. Understand the differences between voluntary and involuntary responses and how the nervous system interacts with other body systems. Ideal for Cambridge IGCSE students preparing for exams!
How could modern LA research address data-related ethics issues in informal and situated professional learning? I will identify in this talk three relevant insights based on field studies around workplace LA interventions: Firstly, in informal and situated learning, data isn’t just about the learners. Secondly, the affordances of manual and automatic data tracking for learning are very different, with manual tracking allowing a high degree of learner control over data. Thirdly, learning is not necessarily a shared goal in workplaces. These can be translated into seeing a potential for systems endowed with sufficient natural-language-processing capability (now seemingly at our fingertips with LLMs), and socio-technical design and scenario-based data collection analysis as design and research methods.
The Solar System’s passage through the Radcliffe wave during the middle MioceneSérgio Sacani
As the Solar System orbits the Milky Way, it encounters various Galactic environments, including dense regions of the
interstellar medium (ISM). These encounters can compress the heliosphere, exposing parts of the Solar System to the ISM, while also
increasing the influx of interstellar dust into the Solar System and Earth’s atmosphere. The discovery of new Galactic structures, such
as the Radcliffe wave, raises the question of whether the Sun has encountered any of them.
Aims. The present study investigates the potential passage of the Solar System through the Radcliffe wave gas structure over the past
30 million years (Myr).
Methods. We used a sample of 56 high-quality, young (≤30 Myr) open clusters associated with a region of interest of the Radcliffe
wave to trace its motion back and investigate a potential crossing with the Solar System’s past orbit.
Results. We find that the Solar System’s trajectory intersected the Radcliffe wave in the Orion region. We have constrained the timing
of this event to between 18.2 and 11.5 Myr ago, with the closest approach occurring between 14.8 and 12.4 Myr ago. Notably, this
period coincides with the Middle Miocene climate transition on Earth, providing an interdisciplinary link with paleoclimatology. The
potential impact of the crossing of the Radcliffe wave on the climate on Earth is estimated. This crossing could also lead to anomalies
in radionuclide abundances, which is an important research topic in the field of geology and nuclear astrophysics.
Telescope equatorial mount polar alignment quick reference guidebartf25
Telescope equatorial mount polar alignment quick reference guide. Helps with accurate alignment and improved guiding for your telescope. Provides a step-by-step process but in a summarized format so that the quick reference guide can be reviewed and the steps repeated while you are out under the stars with clear skies preparing for a night of astrophotography imaging or visual observing.
History of atomic layer deposition (ALD) in a nutshellRiikka Puurunen
Lecture slides presented at Aalto University course CHEM-E5175 Materials engineering by thin films (by Prof. Ville Miikkulainen), in a visiting lecture Jan 28, 2025
Contents:
1 Invention of Atomic Layer Epitaxy 1974
2 Microchemistry Ltd and spread of ALE/ALD
3 Independent invention, Molecular Layering 1960s -->
4 Connecting the two independent development branches of ALD
5 Take-home message
(Extra materials on fundamentals of ALD, assumed as background knowledge)
SlideShare: https://www.slideshare.net/slideshow/history-of-atomic-layer-deposition-ald-in-a-nutshell/275984811
Youtube: https://youtu.be/FBLThDjRff0
History of atomic layer deposition (ALD) in a nutshellRiikka Puurunen
Western Blotting Technique.
1. RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 1
A Seminar as a part of curricular requirement for
M . Pharmacy I year I Semester
Presented by
T. Niranjan Reddy
(20L81S0109)
Department of Pharmacology
Under the guidance of
Dr. P. Ramalingam, MPharm, Ph. D
Research Director and professor of Pharmaceutical and medicinal
chemistry
WESTERN BLOTTING
2. RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
Contents :
Introduction
Types of blotting techniques
Principle of western blotting
Procedure for western blotting
Gel electrophoresis
Protein transfer
Antibody probing
Protein detection
Analysis and imaging
Applications
Limitations
2
3. RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
Introduction:
Blotting
Blotting is a method of transferring proteins, DNA or
RNA, on to a carrier (for example, a nitrocellulose or
PVDF or nylon membrane)
3
4. RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
5. RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
Western blotting is a widely used analytical technique in molecular
biology to detect specific protein in a sample of tissue homogenate
or the extract
It works on the principle of gel electrophoresis
Proteins are separated based on their size on polyacrylamide gel
Western blotting
6. RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 6
• Western blotting is an immunoblotting technique which rely on the
specificity of bonding between a molecule of interest and a probe to
allow detection of the molecule of interest in a mixture of many
other similar molecules
• In western blotting, the molecule of interest is a protein and the
probe is typically an antibody raised against that particular protein
• The SDS PAGE (sodium dodecyl sulphate –polyacrylamide gel )
technique is a prerequisite for western blotting.
Principle of western blotting
7. RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 7
8. RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 8
9. RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 9
• The proteins of the sample are separated by using the gel
electrophoresis
• Electrophoresis is a commonly used method for separating proteins
on the basis of size, shape and charge
• In SDS (sodium dodecyl sulphate) electrophoresis, protein samples
are separated according to their molecular weight.
Gel electrophoresis
10. RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 10
Page protocol
11. RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
Sample Loading
11
12. RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 12
On completion of the separation of proteins by polyacrylamide gel
electrophoresis, the next step is to transfer the proteins from the gels to
solid support membrane
This solid support membrane usually made up of a chemically inert
substance such as nitrocellulose or PVDF (polyvinylidene difluoride)
The process of transferring proteins from a gel to a membrane while
maintaining their relative positions and resolutions is known as blotting.
protein transfer:
13. RIPER
AUTONOMOUS
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SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 13
After gel electrophoresis it may be necessary to confirm that all the
proteins in the gel have been completely eluted
As proteins are not directly visible in the gel, the gel must be stained
Proteins are usually stained with dyes such as Coomassie blue, sliver
stain or deep purple
After staining a permanent record may be made by imaging the gel
with the suitable instrument.
Protein staining:
14. RIPER
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SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 14
15. RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
Blocking :
The membrane has the ability to bind to proteins in this case
both the target and antibodies are proteins and so there could
be some unwanted binding.
For meaningful results, the antibodies must bind only to the
protein of interest and not to the membrane
Non specific binding of antibodies can be reduced by
blocking the unoccupied sites of inert protein or non-ionic
protein
Blocking agents should possess greater affinity towards
membrane than the antibodies
15
16. RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 16
The most commonly used blocking agents are :
Bovine serum albumin (BSA)
Non –fat milk
Casein
Gelatine
Dilute solution of tween 20
Blocking agents
17. RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
Antibody probing
After blocking, the blot is incubated with one or more antibodies.
This uses specific antibody to detect a localize the protein blotted to the
membrane
The specificity of antigen antibody permits the identification of a single protein
in a complex sample
The non-labelled primary antibody directed against the target protein and
specific labelled secondary antibody binds to primary antibody
The secondary antibody is conjugated to an enzyme that is used to indicate the
location of protein
Secondary antibodies can be a monoclonal or polyclonal antibodies
17
18. RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
Washing
• The unbound antibodies can cause high background and poor
detection
• Hence, washing the blot removes unbound antibodies from the
membrane
• A dilute solution of tween – 20 in TBS or PBS buffer is
commonly used for washing
18
19. RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
Protein detection
• After the unbound probes are washed away, the western
blotting is now ready for detection of probes that are labelled
and bound to the protein of interest
• The marked antibody which is linked to a reporter enzyme
which when exposed to appropriate substrate drives a
colorimetric reaction and produces a colour
• Enzymes such as alkaline phosphatase(AP) and horse radish
peroxidase (HRP) are widely used in detection of proteins
20. RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 20
21. RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 21
This is the last and major step of the western blotting technique
Detection of signals using either x-ray film, scanners or a CCD,
results in one or more visible proteins on the membrane image
The molecular weight of protein can be estimated by comparison
with marker proteins and the amount of protein can be determined
and this is related to band intensity
Qualitative and quantitative analysis can be done in order to verify
the absence or presence of specific proteins of interest.
Analysis and imaging
22. RIPER
AUTONOMOUS
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NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 22
Analysis of igG fractions purifies from human plasma
Diagnosis of HIV by ELISA, involves the western blotting technique
Western blotting technique is also used to detect some forms of
Lyme disease
Western blotting technique is used in definitive test for BSE, which
is commonly known as mad cow disease
confirmatory test for hepatitis-B involves western blotting
technique
This technique are employed in the gene expression studies.
Application of Western Blotting
23. RIPER
AUTONOMOUS
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SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 23
Very delicate and time consuming process
If a protein is degraded quickly, then western blotting technique
wont detect it well
Well trained techniques are required for this technique
Primary antibody availability is crucial.
Limitations of Western Blotting
24. RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
References :
• Kurien BT, Scofield RH. 2006. Western blotting. Methods 38: 283–
293.
• Jensen EC. The Basics of Western Blotting. Anat Rec. 2012
Mar 1;295(3):369–71.
• Antharavally BS, et al. A high-affinity reversible protein stain
for Western blots. Analytical biochemistry. 2004;329(2):276–
80
24
25. RIPER
AUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 25