1 SURVEY OF BIOCHEMISTRY Nucleic Acids continued… Amino Acids.

Slides:



Advertisements
Similar presentations
Chapter 20 DNA Technology & Genomics. Slide 2 of 14 Biotechnology Terms Biotechnology Process of manipulating organisms or their components to make useful.
Advertisements

Polymerase Chain Reaction (PCR)
Sequencing Using DNA dependant DNA polymerase Initiation & elongation commences Denature & anneal labelled primer * * dCTP dGTP dATP dTTPdCTP dATP dTTPdATP.
Polymerase Chain Reaction (PCR). PCR produces billions of copies of a specific piece of DNA from trace amounts of starting material. (i.e. blood, skin.
COMPUTER EXERCISE Design of PCR and PCR-RFLP experiments This presentation shows all steps of a PCR-RFLP experiment and is a companion of the computer.
PCR Basics Purpose of PCR Overview Components of PCR Reaction
PCR Basics 1.Purpose of PCR 2.Overview 3.Components of PCR Reaction 4.Variables Temperature Cycle Times and Numbers Primer Buffer Polymerase 5.Experimental.
PCR Polymerase Chain Reaction. PCR - a method for amplifying (copying) small amount of DNA in nearly any amount required, starting with a small initial.
MCB 130L Lecture 1: DNA.
MCB 130L Lecture 1 1. How to get the most from your time in lab 2. Recombinant DNA 3. Tips on giving a Powerpoint talk.
Lab 8: PCR (Polymerase Chain Reaction)
What are the three steps in PCR?. Denaturation Hybridization of Primer DNA replication.
Polymerase chain reaction
Polymerase Chain Reaction
Mutation  Is a change in the genetic material.  Structural change in genomic DNA which can be transmitted from cell to it is daughter cell.  Structural.
Chromosome 16: PV92 PCR. What is PCR? DNA replication gone crazy in a tube!DNA replication gone crazy in a tube! Makes many copies of target sequence.
Objective 2: TSWBAT describe the basic process of genetic engineering and the applications of it.
AP Biology: Chapter 14 DNA Technologies
Recombinant DNA Technology……….. BTEC3301. DNA Libraries How do you identify the gene of interest and clone only the DNA sequence you are interested? Read.
PV92 PCR/Informatics Kit
Announcements Lab notebooks due Monday by 5 No Ch. 9 Part 2 homework
Polymerase Chain Reaction. PCR Repetitive amplification of a piece or region of DNA Numerous uses –Straightforward amplification & cloning of DNA –RT-PCR.
Polymerase Chain Reaction PCR. invented by Karry B. Mullis (1983, Nobel Prize 1993) patent sold by Cetus corp. to La Roche for $300 million depends on.
Polymerase Chain Reaction (PCR)
Module 1 Section 1.3 DNA Technology
Week #1CHEM Summer SURVEY OF BIOCHEMISTRY Nucleic Acids.
CHMI 4226E - W20051 Recombinant DNA Technology CHMI 4226 E Week of March 2, 2009 Mutagenesis.
PCR Forensics. Today’s Lab There has been an outbreak of Salmonella poisoning in the Student Union cafeteria at Stanford University cafeteria. You have.
 DNA (gene mutations, paternity, organs compatibility for transplantations)  RNA  Proteins (gene expression)
Polymerase Chain Reaction (PCR) Developed in 1983 by Kary Mullis Major breakthrough in Molecular Biology Allows for the amplification of specific DNA fragments.
It is a technique used to produce large quantities of replicated DNA.
A story about Section 2. What is PCR? Polymerase Chain Reaction A method to synthesis specific DNA fragment in vitro. It is composed of many cycles including.
The polymerase chain reaction
Nucleotides and Nucleic Acids. Cellular Processes DNA RNA (mRNA) Proteins LipidsCarbohydrates replication transcription translation.
Primer extension * This labelling technique uses random oligonucleotides (usually hexadeoxyribonucleotide molecules- sequences of six deoxynucleotides)
A program of ITEST (Information Technology Experiences for Students and Teachers) funded by the National Science Foundation Background Session #5 Polymerase.
More Basic Biotechnology Tools Sorting & Copying DNA.
The polymerase chain reaction
Sanger or Dideoxy DNA Sequencing
PCR With PCR it is possible to amplify a single piece of DNA, or a very small number of pieces of DNA, over many cycles, generating millions of copies.
The Polymerase Chain Reaction (PCR)
Polymerase Chain Reaction (PCR)
Lab 22 Goals and Objectives: EDVOKIT#300: Blue/White Cloning of a DNA Fragment Calculate transformation efficiencies Compare control efficiency to cloned.
710.LC GRADUATE MOLECULAR BIOLOGY 10/31/2011. Lecture 4 Competency Test.
Lecture 4: Polymerase Chain Reaction (PCR)
DNA Isolation. Nucleic Acid Structure & Function DNA & RNA are composed of Nucleotides A nucleotide consists of three covalently-linked parts: –A nitrogen.
Lecturer: Bahiya Osrah Background PCR (Polymerase Chain Reaction) is a molecular biological technique that is used to amplify specific.
Gene Cloning 분자생물학실험 이효민 DNA Cloning DNA cloning is a technique for reproducing DNA fragments. It can be achieved by two different approaches:
I. PCR- Polymerase Chain Reaction A. A method to amplify a specific piece of DNA. DNA polymerase adds complementary strand DNA heated to separate strands.
Polymerase Chain Reaction (PCR). DNA DNA is a nucleic acid that is composed of two complementary nucleotide building block chains. The nucleotides are.
Polymerase Chain Reaction. Before PCR Before PCR Recombinant Recombinant DNA DNA technology technology.
Presented by: Khadija Balubaid.  PCR (Polymerase Chain Reaction) is a molecular biological technique  used to amplify specific fragment of DNA in vitro.
The stroke size should be 0.25
PCR Basics Purpose of PCR Overview Components of PCR Reaction
SURVEY OF BIOCHEMISTRY Nucleic Acids continued… Amino Acids
SURVEY OF BIOCHEMISTRY Nucleic Acids
Jeopardy Final Jeopardy Gene Cloning Plasmids Ligase PCR $100 $100
Polymerase Chain Reaction (PCR)
PCR Polymerase Chain Reaction
Alu insert, PV92 locus, chromosome 16
Molecular Cloning: Polymerase Chain Reaction
Polymerase Chain Reaction
Polymerase Chain Reaction
PCR How does PCR work?: Separation of two strands
Polymerase Chain Reaction (PCR)
Screening a Library for Clones Carrying a Gene of Interest
DNA-based technology New and old technologies that are utilized in biotechnology DNA cloning DNA libraries Polymerase chain reaction (PCR) Genome sequencing.
710.LC GRADUATE MOLECULAR BIOLOGY 10/31/2011
710.LC GRADUATE MOLECULAR BIOLOGY 9/15/2010
Bioinformatics Lecture By: Ms AQSAD RASHDA
Presentation transcript:

1 SURVEY OF BIOCHEMISTRY Nucleic Acids continued… Amino Acids

2 PRS Question Name the following compound 1.ATP 2.UTP 3.GTP 4.CTP

3 PRS Question Thymine has a methyl group at which position? 1.C1 2.C3 3.C5 4.C1’

4 Last Week… Recombinant DNA Technology –Vectors, Cloning and Libraries Genomic vs. cDNA Library How are libraries made? –PCR (for making copies of DNA) How does PCR work? What is required to conduct PCR?

5 Genomic Library Cut Genomic DNA with restriction enzymes Insert fragments into vectors Culture cells Reference: Wikipedia

6 Making cDNA Image from Biochemistry by Stryer

7 Making cDNA Clones Image from Biochemistry by Stryer

8 3 steps for each PCR cycle Each PCR cycle includes: –A denaturation step (92-96 o C) separates the two DNA strands. –A primer annealing step (40-75 o C) which is a few degrees below the T m of the primers. –A primer extension step (72 o C) which is the optimal temperature for Taq DNA polymerase activity.

9 Components for PCR  Heat-stable DNA polymerase Thermus aquaticus Taq polymerase  Primers (DNA oligonucleotides)  Deoxynucleotides –dATP, dTTP, dCTP, dGTP  DNA template  Mg ++, buffer components, and water KNOW THIS!!