PCR Related Products.

Slides:



Advertisements
Similar presentations
Polymerase Chain Reaction
Advertisements

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.
Generating the histone code CDK8 kinases histones to repress transcription.
Primer/probe design Crucial for successful DNA & RNA analysis! Main source of specificity for PCR.
Polymerase Chain Reaction (PCR) and Its Applications by Ayaz Najafov Boğaziçi University Department of Molecular Biology and Genetics.
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.
I-5-1 Basic Principles and Components of PCR NSYSU CHUNG-LUNG CHO.
PCR Polymerase Chain Reaction. PCR - a method for amplifying (copying) small amount of DNA in nearly any amount required, starting with a small initial.
1 Characterization, Amplification, Expression Screening of libraries Amplification of DNA (PCR) Analysis of DNA (Sequencing) Chemical Synthesis of DNA.
General Genetics. PCR 1.Introduce the students to the preparation of the PCR reaction. PCR 2.Examine the PCR products on agarose gel electrophoresis.
PCR Optimization: Challenges and Successes May 8, 2009 DNA Facility Seminar Series.
ZmqqRPISg0g&feature=player_detail page The polymerase chain reaction (PCR)
Long PCR Yanfei Yang Compromise of longer PCR (>3,4kb) Nonspecific primer annealing Suboptimal cycling conditions Secondary structures in the.
Accuracy: The closeness of a measured volume to the true volume as specified by the volume setting of the pipette. Also known as “mean error”. precision:
Polymerase Chain Reaction
WORKSHOP (1) Presented by: Afsaneh Bazgir Polymerase Chain Reaction
PCR- Polymerase chain reaction
PCR and qRT-PCR May 3. PCR The thermocycle analyzing the products essential components of the reaction optimization basic rules of primer design problems.
Recombinant DNA Technology………..
Polymerase Chain Reaction. PCR Repetitive amplification of a piece or region of DNA Numerous uses –Straightforward amplification & cloning of DNA –RT-PCR.
What do these terms mean to you? You have 5 min to discuss possible meanings and examples with your group! DNA sequencing DNA profiling/fingerprinting.
CHMI 4226E – W20051 Recombinant DNA Technology CHMI 4226 E Week 3 19 January 2009 Toolbox part 3 PCR.
The Polymerase Chain Reaction
PCR Troubleshooting Virginia Balke
Polymerase Chain Reaction PCR. PCR allows for amplification of a small piece of DNA. Some applications of PCR are in: –forensics (paternity testing, crimes)
CHMI 4226E - W20051 Recombinant DNA Technology CHMI 4226 E Week of March 2, 2009 Mutagenesis.
Properties of Thermostable DNA Polymerase Yufei TU Yufei TU.
Polymerase Chain Reaction (PCR) Developed in 1983 by Kary Mullis Major breakthrough in Molecular Biology Allows for the amplification of specific DNA fragments.
©2001 Timothy G. Standish Romans 5:17 17For if by one man’s offence death reigned by one; much more they which receive abundance of grace and of the gift.
PCR is used in; Cloning into plasmid vectors DNA sequencing Genetic screening DNA based phylogeny Functional analysis of genes Identification of DNA fingerprints.
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.
A program of ITEST (Information Technology Experiences for Students and Teachers) funded by the National Science Foundation Background Session #5 Polymerase.
Section J Analysis and application of cloning DNA.
The polymerase chain reaction
Polymerase Chain Reaction: “DNA Photocopying” SBI4U AP Mr. McCrorie.
Polymerase Chain Reaction A process used to artificially multiply a chosen piece of genetic material. May also be known as DNA amplification. One strand.
1 SURVEY OF BIOCHEMISTRY Nucleic Acids continued… Amino Acids.
The Polymerase Chain Reaction (PCR)
Introduction to PCR Polymerase Chain Reaction
Lab 22 Goals and Objectives: EDVOKIT#300: Blue/White Cloning of a DNA Fragment Calculate transformation efficiencies Compare control efficiency to cloned.
PKS Plasmid : 20 ul 10XTango Buffer : 3 ul SmaI (1u/ul) : 1 ul Distilled dH2O : 6 ul 30 ul.
Restriction Enzyme Store in -20 C Digestion. Restriction Enzyme Buffer NaCl or KCl, TrisHCl, MgCl 2, DTT Different salt: varied activity Buffer supplied.
Components Of A Typical PCR Reaction Mix PCR Reaction Buffer (usually supplied at 10X) 100mM Tris-HCl - Essentially a pH Buffer. Maintains appropriate.
Lecturer: Bahiya Osrah Background PCR (Polymerase Chain Reaction) is a molecular biological technique that is used to amplify specific.
Rajan sharma.  Polymerase chain reaction Is a in vitro method of enzymatic synthesis of specific DNA sequences.  This method was first time developed.
M Gradient PCR using Taq polymerase with 125ng primer concentration M: 1 kb ladder 1: 60°C 2: 62°C 3: 64.4°C 4:66.8°C 5: 69.2°C 6:71.5°C 284D.
GoTaq DNA Polymerase GoTaq Flexi DNA Polymerase GoTaq Green Master Mix GoTaq Green Hot Start Master Mix GoTaq Colorless Master Mix GoTaq Colorless Hot.
The PCR Buffer.
Polymerase Chain Reaction (PCR). DNA DNA is a nucleic acid that is composed of two complementary nucleotide building block chains. The nucleotides are.
January 19, 2016 Biotech 3 Lecture Annealing 1. Melting 3. Elongation 4. Repeat cycle ~ 30 times Polymerase Chain Reaction.
Basic Tools: Recombinant DNA Techniques Cut Purified DNA with Restriction Enzymes Transform E. coli Purified plasmid DNA Various restriction enzymes T4.
Presented by: Khadija Balubaid.  PCR (Polymerase Chain Reaction) is a molecular biological technique  used to amplify specific fragment of DNA in vitro.
Introduction to PCR Polymerase Chain Reaction
PCR Basics Purpose of PCR Overview Components of PCR Reaction
SURVEY OF BIOCHEMISTRY Nucleic Acids continued… Amino Acids
Topics to be covered Basics of PCR
Polymerase Chain Reaction (PCR)
Directed Mutagenesis and Protein Engineering
Polymerase Chain Reaction
Polymerase Chain Reaction
Polymerase Chain Reaction
Polymerase Chain Reaction
Molecular Biology lecture -Putnoky
Phenylthiocarbamide (PTC)
Polymerase Chain Reaction (PCR).
Course Project Engineering electricity production by plants
PCR Polymerase chain reaction (PCR)
Presentation transcript:

PCR Related Products

Current Products Thermostable DNA polymerases TaqExtender Pfu PfuTurbo TaqPlus Precision TaqPlus Long Taq TaqExtender Perfect Match Opti-Prime

Components of PCR Thermostable DNA polymerase Reaction Buffer Primers Template DNA dNTPs Water Cycling Conditions Each component affects the quality of the PCR

PCR Qualities Yield Fidelity Specificity Length These are the qualities that we can measure and optimize. Usually one quality has to be sacrificed to improve another.

Thermostable DNA polymerases Pfu PfuTurbo TaqPlus Precision TaqPlus Long Taq

error rate extension Recommended PCR Target (x10 ) time Length (kb) -6 ) time Length (kb) required (min/kb vector genomic target) targets targets PfuTurbo DNA 1.3 + 0.2 1 0-10 0-6 polymerase 2 0-15 0-10 Pfu DNA 1.3 + 0.2 2 0-10 0-4 polymerase TaqPlus 3.9 + 1.3 1 0-15 0-10 Precision system TaqPlus Long 7.6 + 1.2 0.5-1 0-35 0-18.5 system Taq DNA 8.0 + 3.9 1 0-10 0-5 polymerase

Functional Domains of Pfu DNA Polymerase 5’-3’ exo DNA-dependent DNA polymerase 3’-5’ exo 1 126 329 775 non- functional proofreading DNA synthesis activity

Fidelity Assay PCR Mutations are detected in the lacI gene not single round extension Mutations are detected in the lacI gene Color detection from Big Blue system Results have been published in peer reviewed journals

Characteristics of Pfu High Fidelity Native Hot Start activity High Thermostability Slow polymerization rate Available as native and cloned enzyme

Accuracy of Polymerases in PCR

Extension Time Pfu requires 2 min/kb Minutes of extension time/kb of PCR target M 0.25 0.5 1 1.5 2 2.5 3 3.5 4 Taq Pfu

Activity vs Temperature Pfu and Taq percent activity 25 35 50 60 75 95 Incubation Temperature (degrees C)

Pfu: Hot Start Every Cycle M T TS ATG TMg Pfu

Polymerase Thermostability DNA Polymerase Polymerization Opt Half Life 95oC Pfu 70-80oC 19 hours Taq 70-80oC 1 hour

Characteristics of PfuTurbo Improved version of Pfu Same high fidelity as Pfu Higher PCR product yield than Pfu alone Can use 1 min/kb extension times Works well with low amounts of DNA template

PCR Enhancing Factor (PEF) Isolated from Pyrococcus Lacks DNA polymerase and exonuclease activities Information on identity/mechanism of action is proprietary

PfuTurbo vs Other Polymerases M PT P V DV Pw K T M PT P V DV Pw K T M 5.2 kb 0.9 kb

PfuTurbo vs Pfu M T P T P T P T P T P 8 kb 6.1 kb 5.2 kb 1.9 kb 0.9 kb

Characteristics of TaqPlus Precision Blend of Taq and Pfu High Yield High Fidelity Length PCR Buffer optimized for both yield and fidelity

Accuracy of Polymerase Blends in PCR

PCR with TaqPlus Precision vs Taq Taq TaqPlus Precision M 2 5.2 5.4 10 15 M 2 5.2 5.4 10 15 kb

Characteristics of TaqPlus Long Blend of Taq and Pfu Long targets Fidelity similar to Taq Two optimal buffers supplied high salt buffer helps prevent smearing in long target amplification low salt buffer

PCR with Taq vs TaqPlus Long

Qualities of Taq Taq2000 is the recombinant Taq Native Taq is also available Taq is trusted by customers Taq has been well studied

TaqExtender The Pfu component of TaqPlus Long Can be added to any Taq to make a polymerase blend

Perfect Match PCR Enhancer Taq2000 native Taq M - + - +

Opti-Prime PCR Optimization Kit 12 buffers matrix of pH, Mg, KCl Adjuncts DMSO, formamide, BSA, glycerol, ammonium sulfate, Perfect Match Recommended for use with Taq

Related PCR products RoboCycler Nucleotides and primers gradient Nucleotides and primers StrataPrep PCR purification kit Cloning Vectors PCR-Script Kits Affinity protein expression kit QuikChange site-directed mutagenesis kit Cyclist DNA sequencing kits