Gene cloning involves producing exact copies of a gene using genetic engineering techniques. It involves isolating the gene of interest from one organism and inserting it into a vector, which is then introduced into a host organism where the gene can be replicated. There are several methods used to transfer genes between organisms or cells, including bacterial transformation, electroporation, transfection, and microinjection. Bacterial transformation involves directly taking up exogenous DNA, electroporation uses an electric pulse to create pores for DNA entry, while transfection introduces nucleic acids into eukaryotic cells using chemical reagents or viruses.
This document discusses various techniques for gene transfer, including natural methods like conjugation, transformation, and transduction, as well artificial methods like microinjection, biolistics, calcium phosphate transfection, liposome-mediated transfection, and electroporation. It provides details on how each method works, such as how conjugation involves transfer of DNA between bacteria via sex pili, how transformation involves direct DNA uptake by competent bacteria, and how transduction involves transfer of DNA between bacteria via bacteriophages. The document also discusses Agrobacterium-mediated plant transformation and applications of gene transfer techniques.
This document discusses various techniques for gene transfer, including natural methods like conjugation, transformation, and transduction, as well artificial methods like microinjection, biolistics, calcium phosphate and liposome mediated transfer, and electroporation. It provides details on how each method works, such as how conjugation involves transfer of DNA between bacteria via sex pili, and how electroporation uses electrical pulses to create pores in cell membranes to allow DNA entry. The document also summarizes screening and applications of transgenic techniques.
This document discusses various methods of transfection, which is defined as the introduction of foreign DNA into eukaryotic cells. It describes transfection methods such as calcium phosphate transfection, liposome-mediated transfection, retroviral transfection, and electroporation. It provides details on how each method works and compares their strengths and weaknesses. Common transfection methods like calcium phosphate and liposomes are simple but have low efficiency, while retroviral transfection can generate stable cell lines but has limitations on DNA size. Electroporation is fast and applicable to many cell types.
This document summarizes transduction and transfection techniques used to introduce foreign DNA into bacterial and animal cells. It discusses that transduction involves the transfer of DNA between bacteria using bacteriophages, occurring through either the lytic or lysogenic cycle. Generalized transduction transfers random bacterial DNA, while specialized transduction transfers specific DNA depending on phage location. Transfection introduces nucleic acids into animal cells using physical or chemical methods like lipofection, electroporation, or particle bombardment to open pores for DNA uptake. Lipofection uses cationic lipids to form DNA-lipid complexes, while electroporation uses an electric field to create membrane pores.
Gene transfer techniques can be used to transfer genes between organisms. There are natural methods like conjugation, transformation, and transduction that transfer genes between bacteria. Artificial methods like microinjection, biolistics, calcium phosphate transfection, liposome transfection, and electroporation can be used to transfer genes into both bacteria and eukaryotic cells. Agrobacterium mediated transfer is used to transfer genes into plant cells and involves the T-DNA region of the Ti plasmid. The transferred gene is then integrated into the host genome.
This document summarizes non-viral gene transfer techniques. It discusses that gene expression is the process by which genetic information is used to produce functional products like proteins. Gene therapy techniques use genes to treat diseases by delivering transgenes into cells. Non-viral methods of gene transfer include chemical methods like oligonucleotides, liposomes, lipoplexes, and polymersomes, as well as physical methods like gene guns, electroporation, sonoporation, magnetofection, and hydrodynamic delivery. These non-viral methods facilitate intracellular delivery of DNA through mechanisms like forming transient pores in cell membranes.
Gene cloning involves producing exact copies of a gene using genetic engineering techniques. It involves isolating the gene of interest from one organism and inserting it into a vector, which is then introduced into a host organism where the gene can be replicated. There are several methods used to transfer genes between organisms or cells, including bacterial transformation, electroporation, transfection, and microinjection. Bacterial transformation involves directly taking up exogenous DNA, electroporation uses an electric pulse to create pores for DNA entry, while transfection introduces nucleic acids into eukaryotic cells using chemical reagents or viruses.
This document discusses various techniques for gene transfer, including natural methods like conjugation, transformation, and transduction, as well artificial methods like microinjection, biolistics, calcium phosphate transfection, liposome-mediated transfection, and electroporation. It provides details on how each method works, such as how conjugation involves transfer of DNA between bacteria via sex pili, how transformation involves direct DNA uptake by competent bacteria, and how transduction involves transfer of DNA between bacteria via bacteriophages. The document also discusses Agrobacterium-mediated plant transformation and applications of gene transfer techniques.
This document discusses various techniques for gene transfer, including natural methods like conjugation, transformation, and transduction, as well artificial methods like microinjection, biolistics, calcium phosphate and liposome mediated transfer, and electroporation. It provides details on how each method works, such as how conjugation involves transfer of DNA between bacteria via sex pili, and how electroporation uses electrical pulses to create pores in cell membranes to allow DNA entry. The document also summarizes screening and applications of transgenic techniques.
This document discusses various methods of transfection, which is defined as the introduction of foreign DNA into eukaryotic cells. It describes transfection methods such as calcium phosphate transfection, liposome-mediated transfection, retroviral transfection, and electroporation. It provides details on how each method works and compares their strengths and weaknesses. Common transfection methods like calcium phosphate and liposomes are simple but have low efficiency, while retroviral transfection can generate stable cell lines but has limitations on DNA size. Electroporation is fast and applicable to many cell types.
This document summarizes transduction and transfection techniques used to introduce foreign DNA into bacterial and animal cells. It discusses that transduction involves the transfer of DNA between bacteria using bacteriophages, occurring through either the lytic or lysogenic cycle. Generalized transduction transfers random bacterial DNA, while specialized transduction transfers specific DNA depending on phage location. Transfection introduces nucleic acids into animal cells using physical or chemical methods like lipofection, electroporation, or particle bombardment to open pores for DNA uptake. Lipofection uses cationic lipids to form DNA-lipid complexes, while electroporation uses an electric field to create membrane pores.
Gene transfer techniques can be used to transfer genes between organisms. There are natural methods like conjugation, transformation, and transduction that transfer genes between bacteria. Artificial methods like microinjection, biolistics, calcium phosphate transfection, liposome transfection, and electroporation can be used to transfer genes into both bacteria and eukaryotic cells. Agrobacterium mediated transfer is used to transfer genes into plant cells and involves the T-DNA region of the Ti plasmid. The transferred gene is then integrated into the host genome.
This document summarizes non-viral gene transfer techniques. It discusses that gene expression is the process by which genetic information is used to produce functional products like proteins. Gene therapy techniques use genes to treat diseases by delivering transgenes into cells. Non-viral methods of gene transfer include chemical methods like oligonucleotides, liposomes, lipoplexes, and polymersomes, as well as physical methods like gene guns, electroporation, sonoporation, magnetofection, and hydrodynamic delivery. These non-viral methods facilitate intracellular delivery of DNA through mechanisms like forming transient pores in cell membranes.
Transfection involves introducing foreign DNA into host cells to produce a new phenotype. There are two main methods of transfection - vector-mediated and non-vector mediated. Vector-mediated transfection uses bacteriophage, retroviral, cosmid, baculovirus, and plasmid vectors to introduce DNA. Non-vector mediated methods include direct techniques like microinjection, electroporation, and particle bombardment, and indirect techniques like calcium phosphate precipitation and DEAE-dextran. Retroviral vectors are modified retroviruses that can introduce foreign DNA into host chromosomal DNA. Microinjection involves injecting DNA directly into cells using a micropipette under a microscope. Electroporation uses electric pulses to create temporary
This document discusses various methods of gene transfer, including viral and non-viral methods. Viral methods use recombinant viruses like retroviruses and adenoviruses to insert genes into host cells. Non-viral methods include physical techniques like electroporation and gene guns that force DNA into cells, as well as chemical methods using lipids, polymers, or proteins to transport DNA into cells. Both methods have advantages and disadvantages related to efficiency, safety, and target specificity.
There are three main modes of gene transfer: transformation, transfection, and transduction. Transformation involves the natural uptake of foreign DNA by a cell. Transfection is the deliberate introduction of genetic material into animal cells. Transduction uses viruses to transfer genes between bacterial cells. It can occur through a lysogenic or lytic phase. Conjugation is also discussed, which involves the direct contact and temporary exchange of genetic material between two bacterial cells.
This document discusses non-viral gene transfer methods. It describes various techniques for direct delivery of naked DNA including electroporation, gene guns, sonoporation, magnetofection, hydrodynamic delivery, and microinjections. It also discusses various non-viral vectors for gene delivery including oligonucleotides, liposomes, lipoplexes, polymersomes, polyplexes, dendrimers, inorganic nanoparticles, and cell-penetrating peptides. Each method is described in terms of its mechanism of delivery, advantages, disadvantages and suitable target tissues. The document provides an overview of non-viral gene expression systems and delivery methods.
This document discusses various methods of transfection, which is the process of introducing nucleic acids into cells. It describes both physical and chemical transfection methods. Physical methods include electroporation, microinjection, and cell squeezing, which introduce DNA directly into cells using physical forces. Chemical methods involve using reagents like cationic lipids, calcium phosphate, and cationic polymers to form complexes with DNA that are then taken up by cells. The document discusses the principles, advantages, and disadvantages of many common transfection methods.
This document discusses various gene transfer techniques including physical, chemical, and biological methods. It focuses on biological methods such as bactofection and transduction using viruses. Bactofection involves using bacteria to deliver genes directly into cells, while transduction uses viruses to package and deliver genes. The document also discusses chemical methods like calcium phosphate and lipofection, as well as physical methods such as electroporation, microinjection, and particle bombardment to introduce DNA into host cells.
This document discusses various direct or vectorless gene transfer methods for introducing foreign DNA into plant cells without the use of Agrobacterium. These include chemical methods like PEG-mediated transformation, calcium phosphate precipitation, DEAE-dextran, and liposome-mediated transformation. Physical methods include electroporation, microinjection, and gene guns. The procedures, advantages, and disadvantages of some key methods like PEG-mediated transformation, calcium phosphate precipitation, electroporation, microinjection, and fiber-mediated transformation are described in detail. Direct transformation through imbibition of dehydrated plant tissues is also mentioned.
This document discusses various gene transfer methods. It defines gene transfer as the insertion of genetic material into a cell. There are natural methods like conjugation, transformation, and transduction that involve the transfer of genes between bacteria. There are also artificial physical, chemical, and electrical methods to transfer genes into bacteria, plants, and animals. These include microinjection, biolistics, calcium phosphate, liposomes, and electroporation. The document provides details on how each of these methods work and their advantages and limitations.
This document discusses various vectorless and direct gene transfer methods for recombinant DNA technology. It describes 10 different methods: chemical methods, electroporation, particle bombardment, lipofection, microinjection, macroinjection, pollen transformation, delivery via growing pollen tubes, laser induced transformation, and fibre mediated transformation. Each method directly introduces DNA into host cells without the use of biological vectors. The document provides details on the mechanisms and procedures for several of these direct gene transfer techniques.
Hi, I am RAFi ,student of Genetic Engineering and Biotechnology , Jashore university of science & Technology. It is my first uploading slide in slideshare.I am so glad for doing this work.
This document discusses various gene transfer methods. It defines gene transfer as the insertion of genetic material into a cell. There are natural methods like conjugation, transformation, and transduction that involve the transfer of genes between bacteria. There are also artificial physical, chemical, and electrical methods to transfer genes into cells, including microinjection, gene guns, calcium phosphate, liposomes, and electroporation. The document provides examples of how these various gene transfer methods can be used to insert genes into bacteria, plants, and animals.
Gene delivery is the process of introducing foreign DNA into host cells. There are four principal mechanisms for transferring genes into animal cells: direct physical transfer through microinjection or particle bombardment; chemical-mediated transfection using calcium phosphate or liposomes; transduction using viral vectors; and bactofection using bacterial vectors. Mammalian cells are widely used hosts as they allow production of recombinant human proteins with authentic post-translational modifications. Important applications include gene therapy and producing therapeutic proteins.
DNA Transfection in Animal tissue culture and its methods.pptxMethusharma
You will learn the definition of DNA transfection in this presentation its examples, along with the procedures that are employed, through the use of organised flowcharts and diagrams. The Animal Biotechnology course, it is the first technique to learn.
This document describes various methods for transferring genes into organisms. Biological methods include using viruses like cauliflower mosaic virus (CaMV) to transfer genes into plants. Physical methods include electroporation, which uses electric pulses to create pores in cell membranes through which DNA can enter. Liposomes and direct methods like microinjection and particle bombardment can also be used to directly transfer DNA. Chemical methods involve using compounds like polyethylene glycol (PEG) to destabilize cell membranes and allow DNA uptake. While physical methods can target single cells, they may damage cells. Biological methods using vectors are often more efficient but less controlled. Overall the document provides an overview of the key gene transfer techniques.
This document discusses various methods for transfection of animal cells, which is the process of introducing nucleic acids into eukaryotic cells. It describes transfection techniques including calcium phosphate co-precipitation, electroporation, lipofection, viral vectors, and microinjection. The purpose of transfection is to study gene function and protein expression or transfer DNA into embryonic stem cells. Common methods involve using chemicals, lipids, electricity, or viruses to transport DNA/RNA across the cell membrane or directly injecting it using a micropipette.
Transfection methods (DNA to host cell) Erin Davis
Transfection of DNA to host cell can be done by various methods in lab scale.Gene gun,electroporation,lipofection .These methods are used to transfer DNA to the host cell.
This document summarizes gene expression systems, including both nonviral and viral gene transfer methods. It defines gene expression as the process by which information in DNA is used to produce a functional gene product like a protein. Nonviral methods include injecting naked DNA, as well as using physical methods like electroporation or chemical methods like lipoplexes to enhance DNA delivery into cells. Viral vectors are more efficient at transferring genes into cells and work by infecting cells with modified viruses that deliver therapeutic genes. Common viral vectors discussed are adenoviral, retroviral, and adeno-associated viral vectors.
This document discusses various techniques for introducing DNA into target organs, including chemical methods like DEAE-dextran and calcium-phosphate coprecipitation, physical methods like biolistic particle delivery and microinjection, and biological methods like Agrobacterium-mediated transformation. It provides details on the principles and advantages and disadvantages of each method.
Transfection in animal cells through chemical methods like Calcium phosphate ...SmritiRanjan9
The document summarizes various methods for transfecting animal cells, including calcium phosphate coprecipitation, lipofection, electroporation, viral vectors, microinjection, and direct DNA transfer. It provides details on the mechanisms and advantages/disadvantages of each method. Calcium phosphate transfection involves precipitating DNA with calcium phosphate to facilitate cell binding and entry. Lipofection uses cationic lipids to form complexes with nucleic acids for cellular uptake. Electroporation exposes cells to electric pulses to temporarily destabilize membranes and allow DNA entry. Viral vectors are highly efficient but require biosafety precautions. Microinjection and gene guns directly inject or bombard DNA into cells.
This document discusses various techniques for transferring genes, including natural and artificial methods. Natural methods include conjugation, transformation, transduction, and Agrobacterium-mediated transfer. Artificial methods include microinjection, biolistics, calcium phosphate transfection, liposome-mediated transfer, and electroporation. The document provides detailed descriptions of conjugation, transformation, transduction, Agrobacterium-mediated transfer, microinjection, biolistics, calcium phosphate transfection, liposome-mediated transfer, and electroporation. It also discusses screening methods for transgenes and applications of gene transfer techniques.
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Transfection involves introducing foreign DNA into host cells to produce a new phenotype. There are two main methods of transfection - vector-mediated and non-vector mediated. Vector-mediated transfection uses bacteriophage, retroviral, cosmid, baculovirus, and plasmid vectors to introduce DNA. Non-vector mediated methods include direct techniques like microinjection, electroporation, and particle bombardment, and indirect techniques like calcium phosphate precipitation and DEAE-dextran. Retroviral vectors are modified retroviruses that can introduce foreign DNA into host chromosomal DNA. Microinjection involves injecting DNA directly into cells using a micropipette under a microscope. Electroporation uses electric pulses to create temporary
This document discusses various methods of gene transfer, including viral and non-viral methods. Viral methods use recombinant viruses like retroviruses and adenoviruses to insert genes into host cells. Non-viral methods include physical techniques like electroporation and gene guns that force DNA into cells, as well as chemical methods using lipids, polymers, or proteins to transport DNA into cells. Both methods have advantages and disadvantages related to efficiency, safety, and target specificity.
There are three main modes of gene transfer: transformation, transfection, and transduction. Transformation involves the natural uptake of foreign DNA by a cell. Transfection is the deliberate introduction of genetic material into animal cells. Transduction uses viruses to transfer genes between bacterial cells. It can occur through a lysogenic or lytic phase. Conjugation is also discussed, which involves the direct contact and temporary exchange of genetic material between two bacterial cells.
This document discusses non-viral gene transfer methods. It describes various techniques for direct delivery of naked DNA including electroporation, gene guns, sonoporation, magnetofection, hydrodynamic delivery, and microinjections. It also discusses various non-viral vectors for gene delivery including oligonucleotides, liposomes, lipoplexes, polymersomes, polyplexes, dendrimers, inorganic nanoparticles, and cell-penetrating peptides. Each method is described in terms of its mechanism of delivery, advantages, disadvantages and suitable target tissues. The document provides an overview of non-viral gene expression systems and delivery methods.
This document discusses various methods of transfection, which is the process of introducing nucleic acids into cells. It describes both physical and chemical transfection methods. Physical methods include electroporation, microinjection, and cell squeezing, which introduce DNA directly into cells using physical forces. Chemical methods involve using reagents like cationic lipids, calcium phosphate, and cationic polymers to form complexes with DNA that are then taken up by cells. The document discusses the principles, advantages, and disadvantages of many common transfection methods.
This document discusses various gene transfer techniques including physical, chemical, and biological methods. It focuses on biological methods such as bactofection and transduction using viruses. Bactofection involves using bacteria to deliver genes directly into cells, while transduction uses viruses to package and deliver genes. The document also discusses chemical methods like calcium phosphate and lipofection, as well as physical methods such as electroporation, microinjection, and particle bombardment to introduce DNA into host cells.
This document discusses various direct or vectorless gene transfer methods for introducing foreign DNA into plant cells without the use of Agrobacterium. These include chemical methods like PEG-mediated transformation, calcium phosphate precipitation, DEAE-dextran, and liposome-mediated transformation. Physical methods include electroporation, microinjection, and gene guns. The procedures, advantages, and disadvantages of some key methods like PEG-mediated transformation, calcium phosphate precipitation, electroporation, microinjection, and fiber-mediated transformation are described in detail. Direct transformation through imbibition of dehydrated plant tissues is also mentioned.
This document discusses various gene transfer methods. It defines gene transfer as the insertion of genetic material into a cell. There are natural methods like conjugation, transformation, and transduction that involve the transfer of genes between bacteria. There are also artificial physical, chemical, and electrical methods to transfer genes into bacteria, plants, and animals. These include microinjection, biolistics, calcium phosphate, liposomes, and electroporation. The document provides details on how each of these methods work and their advantages and limitations.
This document discusses various vectorless and direct gene transfer methods for recombinant DNA technology. It describes 10 different methods: chemical methods, electroporation, particle bombardment, lipofection, microinjection, macroinjection, pollen transformation, delivery via growing pollen tubes, laser induced transformation, and fibre mediated transformation. Each method directly introduces DNA into host cells without the use of biological vectors. The document provides details on the mechanisms and procedures for several of these direct gene transfer techniques.
Hi, I am RAFi ,student of Genetic Engineering and Biotechnology , Jashore university of science & Technology. It is my first uploading slide in slideshare.I am so glad for doing this work.
This document discusses various gene transfer methods. It defines gene transfer as the insertion of genetic material into a cell. There are natural methods like conjugation, transformation, and transduction that involve the transfer of genes between bacteria. There are also artificial physical, chemical, and electrical methods to transfer genes into cells, including microinjection, gene guns, calcium phosphate, liposomes, and electroporation. The document provides examples of how these various gene transfer methods can be used to insert genes into bacteria, plants, and animals.
Gene delivery is the process of introducing foreign DNA into host cells. There are four principal mechanisms for transferring genes into animal cells: direct physical transfer through microinjection or particle bombardment; chemical-mediated transfection using calcium phosphate or liposomes; transduction using viral vectors; and bactofection using bacterial vectors. Mammalian cells are widely used hosts as they allow production of recombinant human proteins with authentic post-translational modifications. Important applications include gene therapy and producing therapeutic proteins.
DNA Transfection in Animal tissue culture and its methods.pptxMethusharma
You will learn the definition of DNA transfection in this presentation its examples, along with the procedures that are employed, through the use of organised flowcharts and diagrams. The Animal Biotechnology course, it is the first technique to learn.
This document describes various methods for transferring genes into organisms. Biological methods include using viruses like cauliflower mosaic virus (CaMV) to transfer genes into plants. Physical methods include electroporation, which uses electric pulses to create pores in cell membranes through which DNA can enter. Liposomes and direct methods like microinjection and particle bombardment can also be used to directly transfer DNA. Chemical methods involve using compounds like polyethylene glycol (PEG) to destabilize cell membranes and allow DNA uptake. While physical methods can target single cells, they may damage cells. Biological methods using vectors are often more efficient but less controlled. Overall the document provides an overview of the key gene transfer techniques.
This document discusses various methods for transfection of animal cells, which is the process of introducing nucleic acids into eukaryotic cells. It describes transfection techniques including calcium phosphate co-precipitation, electroporation, lipofection, viral vectors, and microinjection. The purpose of transfection is to study gene function and protein expression or transfer DNA into embryonic stem cells. Common methods involve using chemicals, lipids, electricity, or viruses to transport DNA/RNA across the cell membrane or directly injecting it using a micropipette.
Transfection methods (DNA to host cell) Erin Davis
Transfection of DNA to host cell can be done by various methods in lab scale.Gene gun,electroporation,lipofection .These methods are used to transfer DNA to the host cell.
This document summarizes gene expression systems, including both nonviral and viral gene transfer methods. It defines gene expression as the process by which information in DNA is used to produce a functional gene product like a protein. Nonviral methods include injecting naked DNA, as well as using physical methods like electroporation or chemical methods like lipoplexes to enhance DNA delivery into cells. Viral vectors are more efficient at transferring genes into cells and work by infecting cells with modified viruses that deliver therapeutic genes. Common viral vectors discussed are adenoviral, retroviral, and adeno-associated viral vectors.
This document discusses various techniques for introducing DNA into target organs, including chemical methods like DEAE-dextran and calcium-phosphate coprecipitation, physical methods like biolistic particle delivery and microinjection, and biological methods like Agrobacterium-mediated transformation. It provides details on the principles and advantages and disadvantages of each method.
Transfection in animal cells through chemical methods like Calcium phosphate ...SmritiRanjan9
The document summarizes various methods for transfecting animal cells, including calcium phosphate coprecipitation, lipofection, electroporation, viral vectors, microinjection, and direct DNA transfer. It provides details on the mechanisms and advantages/disadvantages of each method. Calcium phosphate transfection involves precipitating DNA with calcium phosphate to facilitate cell binding and entry. Lipofection uses cationic lipids to form complexes with nucleic acids for cellular uptake. Electroporation exposes cells to electric pulses to temporarily destabilize membranes and allow DNA entry. Viral vectors are highly efficient but require biosafety precautions. Microinjection and gene guns directly inject or bombard DNA into cells.
This document discusses various techniques for transferring genes, including natural and artificial methods. Natural methods include conjugation, transformation, transduction, and Agrobacterium-mediated transfer. Artificial methods include microinjection, biolistics, calcium phosphate transfection, liposome-mediated transfer, and electroporation. The document provides detailed descriptions of conjugation, transformation, transduction, Agrobacterium-mediated transfer, microinjection, biolistics, calcium phosphate transfection, liposome-mediated transfer, and electroporation. It also discusses screening methods for transgenes and applications of gene transfer techniques.
Ähnlich wie GENE-TRANSFER-METHODS.pptx.BSFLECTURENOTE (20)
हिंदी वर्णमाला पीपीटी, hindi alphabet PPT presentation, hindi varnamala PPT, Hindi Varnamala pdf, हिंदी स्वर, हिंदी व्यंजन, sikhiye hindi varnmala, dr. mulla adam ali, hindi language and literature, hindi alphabet with drawing, hindi alphabet pdf, hindi varnamala for childrens, hindi language, hindi varnamala practice for kids, https://www.drmullaadamali.com
Gender and Mental Health - Counselling and Family Therapy Applications and In...PsychoTech Services
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ISO/IEC 27001, ISO/IEC 42001, and GDPR: Best Practices for Implementation and...PECB
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Philippine Edukasyong Pantahanan at Pangkabuhayan (EPP) CurriculumMJDuyan
(𝐓𝐋𝐄 𝟏𝟎𝟎) (𝐋𝐞𝐬𝐬𝐨𝐧 𝟏)-𝐏𝐫𝐞𝐥𝐢𝐦𝐬
𝐃𝐢𝐬𝐜𝐮𝐬𝐬 𝐭𝐡𝐞 𝐄𝐏𝐏 𝐂𝐮𝐫𝐫𝐢𝐜𝐮𝐥𝐮𝐦 𝐢𝐧 𝐭𝐡𝐞 𝐏𝐡𝐢𝐥𝐢𝐩𝐩𝐢𝐧𝐞𝐬:
- Understand the goals and objectives of the Edukasyong Pantahanan at Pangkabuhayan (EPP) curriculum, recognizing its importance in fostering practical life skills and values among students. Students will also be able to identify the key components and subjects covered, such as agriculture, home economics, industrial arts, and information and communication technology.
𝐄𝐱𝐩𝐥𝐚𝐢𝐧 𝐭𝐡𝐞 𝐍𝐚𝐭𝐮𝐫𝐞 𝐚𝐧𝐝 𝐒𝐜𝐨𝐩𝐞 𝐨𝐟 𝐚𝐧 𝐄𝐧𝐭𝐫𝐞𝐩𝐫𝐞𝐧𝐞𝐮𝐫:
-Define entrepreneurship, distinguishing it from general business activities by emphasizing its focus on innovation, risk-taking, and value creation. Students will describe the characteristics and traits of successful entrepreneurs, including their roles and responsibilities, and discuss the broader economic and social impacts of entrepreneurial activities on both local and global scales.
Walmart Business+ and Spark Good for Nonprofits.pdfTechSoup
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it describes the bony anatomy including the femoral head , acetabulum, labrum . also discusses the capsule , ligaments . muscle that act on the hip joint and the range of motion are outlined. factors affecting hip joint stability and weight transmission through the joint are summarized.
This document provides an overview of wound healing, its functions, stages, mechanisms, factors affecting it, and complications.
A wound is a break in the integrity of the skin or tissues, which may be associated with disruption of the structure and function.
Healing is the body’s response to injury in an attempt to restore normal structure and functions.
Healing can occur in two ways: Regeneration and Repair
There are 4 phases of wound healing: hemostasis, inflammation, proliferation, and remodeling. This document also describes the mechanism of wound healing. Factors that affect healing include infection, uncontrolled diabetes, poor nutrition, age, anemia, the presence of foreign bodies, etc.
Complications of wound healing like infection, hyperpigmentation of scar, contractures, and keloid formation.
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4. Direct DNA transfer methods rely on
the delivery of naked DNA into the
plant cells. The direct gene transfer can
be broadly divided into two categories.
A. Physical gene transfer methods
• Electroporation
• Microinjection
• Particle bombardment.
5. ELECTROPORATION GENE
TRANSFER
Electroporation can be used to deliver genetic
material into cells that are difficult to transfect.
Electroporation provides consistent and
reproducible results. Electroporation does not
require the use of vectors for gene transfer. It
is a safe and non-toxic method.
6.
7.
8.
9.
10.
11.
12. Liposome-Mediated
Transformation
These liposomes bind and condense DNA
spontaneously to form complexes with
high affinity to cell
membranes. Endocytosis of the complexes
followed by disruption of the endosomal
membrane appears to be the major
mechanism of gene delivery.