اجابة السؤال الاول.

Slides:



Advertisements
Similar presentations
SEQUENCING-related topics 1. chain-termination sequencing 2. the polymerase chain reaction (PCR) 3. cycle sequencing 4. large scale sequencing stefanie.hartmann.
Advertisements

Bacterial Physiology (Micr430)
3 September, 2004 Chapter 20 Methods: Nucleic Acids.
Medical Technology Department, Faculty of Science, Islamic University-Gaza MB M ICRO B IOLOGY Dr. Abdelraouf A. Elmanama Ph. D Microbiology 2008 Chapter.
Biochemistry Ch6. Exploring Gens 阮雪芬 NTUT Oct 14, 2002.
Genetic Engineering Biotechnology Molecular Cloning Recombinant DNA.
Molecular Genetics Introduction to The Structures of DNA and RNA
Cloning, genomes, and proteomes
TOPICS IN (NANO) BIOTECHNOLOGY Lecture 7 5th May, 2006 PhD Course.
Presentation on genome sequencing. Genome: the complete set of gene of an organism Genome annotation: the process by which the genes, control sequences.
Analyzing your clone 1) FISH 2) “Restriction mapping” 3) Southern analysis : DNA 4) Northern analysis: RNA tells size tells which tissues or conditions.
Genetic engineering to produce an organism which will make a ‘foreign’ protein:  Obtain ‘foreign’ gene  Amplify using PCR  Insert gene into a vector.
Chapter 20 DNA Technology and Genomics
Trends in Biotechnology
-The methods section of the course covers chapters 21 and 22, not chapters 20 and 21 -Paper discussion on Tuesday - assignment due at the start of class.
歐亞書局 PRINCIPLES OF BIOCHEMISTRY Chapter 9 DNA-Based Information Technologies.
How do you identify and clone a gene of interest? Shotgun approach? Is there a better way?
Molecular Basis for Relationship between Genotype and Phenotype DNA RNA protein genotype function organism phenotype DNA sequence amino acid sequence transcription.
Biotechnology Packet #12 Chapter #9. Introduction Since the 1970’s, humans have been attempted to manipulate and modify genes in a way that was somewhat.
© 2012 Pearson Education, Inc. Lecture by Edward J. Zalisko PowerPoint Lectures for Campbell Biology: Concepts & Connections, Seventh Edition Reece, Taylor,
DNA Cloning and PCR.
Creating an RNAi feeding vector How does ligation into L4440 work?
Restriction Nucleases Cut at specific recognition sequence Fragments with same cohesive ends can be joined.
Recombinant Technololgy
20.1 Structural Genomics Determines the DNA Sequences of Entire Genomes The ultimate goal of genomic research: determining the ordered nucleotide sequences.
Remember the limitations? –You must know the sequence of the primer sites to use PCR –How do you go about sequencing regions of a genome about which you.
Cutting and Pasting DNA The cutters are called restriction enzymes, they cut DNA at specific nucleotide sequences.
Chapter 6 PCR and in vitro Mutagenesis A. Basic features of PCR 1. PCR is a cell-free method of DNA cloning standard PCR reaction is a selective DNA amplification.
Recombinant DNA Technology. Restriction endonucleases - Blunt ends and Sticky ends.
AP Biology DNA Study Guide. Chapter 16 Molecular Basis of Heredity The structure of DNA The major steps to replication The difference between replication,
Fig Fig Fig Fig Fig
DNA Technology Chapter 11. Genetic Technology- Terms to Know Genetic engineering- Genetic engineering- Recombinant DNA- DNA made from 2 or more organisms.
Biotechnology l Introduction l Tools l Process l Applications.
Chapter 20 DNA Technology and Genomics. Viruses have restriction enzymes to attack and destroy invading viral DNA. Restriction enzymes cut DNA at specific.
Recombinant DNA What is the basis of recombinant DNA technology? How does one “clone” a gene? How are genetically modified organisms (GMOs) created? Illustration.
Molecular Biology II Lecture 1 OrR. Restriction Endonuclease (sticky end)
中国免疫学信息网 SAGE 的原理及其应用 新乡医学院免疫学研究中心 王 辉.
Recombinant DNA Technology. DNA replication refers to the scientific process in which a specific sequence of DNA is replicated in vitro, to produce multiple.
DNA Technology and Genomics
Plasmids that contain l cos sites.
DNA Technology & Genomics
Trends in Biotechnology
A Molecular Toolkit AP Biology Fall The Scissors: Restriction Enzymes  Bacteria possess restriction enzymes whose usual function is to cut apart.
Topic Cloning and analyzing oxalate degrading enzymes to see if they dissolve kidney stones with Dr. VanWert.
BSL2016 / 2018 LEC 8 Genomic Libraries (1) What is a genomic library and why is it important? How does a genomic library differ from a cDNA library? cDNA.
DNA Technology & Genomics CHAPTER 20. Restriction Enzymes enzymes that cut DNA at specific locations (restriction sites) yielding restriction fragments.
Viral and Bacterial Genomes & DNA Technology. Viruses Tiny; much smaller than a bacteria Basic structure: – Nucleic acid (DNA or RNA) enclosed in a protein.
Chapter 13 Nucleic Acid Biotechnology Techniques Mary K. Campbell Shawn O. Farrell Paul D. Adams University.
Topic Cloning and analyzing oxalate degrading enzymes to see if they dissolve kidney stones with Dr. VanWert.
2 Chapter 9 Biotechnology & Recombinant DNA 3 Recombinant Technologies Terminology Recombinant DNA - artificially manipulated DNA Genetic Engineering.
AP EXAM REVIEW SESSION MOLECULAR GENETICS Be prepared, not scared!
Techniques of Molecular Biology
Lecture 8 A toolbox for mechanistic biologists (continued)
DNA Technology and Genomics
Genomics A Systematic Study of the Locations, Functions and Interactions of Many Genes at Once.
Figure 20.0 DNA sequencers DNA Technology.
Chapter 7 Recombinant DNA Technology and Genomics
Dr T-J’s Minilecture Chapter 12.
Material for Quiz 5: Chapter 8
Biotech Tools Review
Chapter 20 – DNA Technology and Genomics
DNA-based technology New and old technologies that are utilized in biotechnology DNA cloning DNA libraries Polymerase chain reaction (PCR) Genome sequencing.
Recombinant DNA Technology
CHAPTER 12 DNA Technology and the Human Genome
Recombinant DNA Technology
KEY CONCEPT Entire genomes are sequenced, studied, and compared.
KEY CONCEPT Entire genomes are sequenced, studied, and compared.
Unit 4: Code of Life Test Review.
KEY CONCEPT Entire genomes are sequenced, studied, and compared.
KEY CONCEPT Entire genomes are sequenced, studied, and compared.
Presentation transcript:

اجابة السؤال الاول

1- Exons and Introns

2- Shine Dalgorne sequence

3- Exonuclease III

4- Restriction endonuclease

5- Alkaline phosphatase

اجابة السؤال الثانى

1- Okasaki fragment

2- Excision repair

3- tRNA

4- Lac operon

5- Real-Time PCR Advantages Real-time PCR enables continuous monitoring of the appearance of the amplified product during the reaction. For measuring levels of a transcript, the process begins with RNA not DNA. Advantages It is the ease and speed of detection of the product Quantifiable Not need gel electrophoresis Useful in diagnostic applications of PCR

5- Real-Time PCR

6- Genomic Libraries A genomic library is a set of recombinant clones that contains the entire DNA present in an individual organism. An E. coli genomic library, for example, contains all the E. coli genes.

6- cDNA libraries

7- Studying a transcriptome by: 7- Studying a Proteome by: Sequence analysis Serial analysis of gene expression (SAGE) Microarray analysis DNA chip analysis 7- Studying a Proteome by: Protein electrophoresis Mass spectrometry

8- Shotgun and Contig Shotgun: insertion of random fragments of DNA into a vector. Contig: DNA sequence built up from a number of smaller overlapping sequences, during a sequencing project

8- Chromosome walking