Beginner s Guide to Real-Time PCR



Similar documents
Real-Time PCR Vs. Traditional PCR

Introduction To Real Time Quantitative PCR (qpcr)

Essentials of Real Time PCR. About Sequence Detection Chemistries

Real-time PCR: Understanding C t

The Techniques of Molecular Biology: Forensic DNA Fingerprinting

DNA and Forensic Science

Hepatitis B Virus. genesig Advanced Kit. DNA testing. Everything... Everyone... Everywhere... Core Protein Region. 150 tests.

Genomic DNA detection assay

2.500 Threshold e Threshold. Exponential phase. Cycle Number

User Manual. CelluLyser Lysis and cdna Synthesis Kit. Version 1.4 Oct 2012 From cells to cdna in one tube

Dengue Virus subtypes 1,2 3 and 4. genesig Standard Kit. DNA testing. Everything... Everyone... Everywhere... 3 Untranslated Region (3 UTR) 150 tests

Real-time quantitative RT -PCR (Taqman)

Thermo Scientific DyNAmo cdna Synthesis Kit for qrt-pcr Technical Manual

Epstein Barr Virus (Human Herpes virus 4) genesig Standard Kit. DNA testing. Everything... Everyone... Everywhere...

VLLM0421c Medical Microbiology I, practical sessions. Protocol to topic J10

Validating Microarray Data Using RT 2 Real-Time PCR Products

Quando si parla di PCR quantitativa si intende:

Epstein Barr Virus (Human Herpes virus 4) nonglycosylated membrane protein (BNRF1) gene. genesig Advanced Kit. DNA testing

AffinityScript QPCR cdna Synthesis Kit

Quantifiler Human DNA Quantification Kit Quantifiler Y Human Male DNA Quantification Kit

Molecular Biology Techniques: A Classroom Laboratory Manual THIRD EDITION

All-in-One mirna qrt-pcr Reagent Kits For quantitative detection of mature mirna

Guide to using the Bio Rad CFX96 Real Time PCR Machine

HiPer RT-PCR Teaching Kit

ab Hi-Fi cdna Synthesis Kit

Human Herpes Virus 1 (Herpes simplex type 1) genesig Standard Kit. DNA testing. Everything... Everyone... Everywhere...

PATHOGEN DETECTION SYSTEMS BY REAL TIME PCR. Results Interpretation Guide

RevertAid Premium First Strand cdna Synthesis Kit

Co Extra (GM and non GM supply chains: Their CO EXistence and TRAceability) Outcomes of Co Extra

QPCR Applications using Stratagene s Mx Real-Time PCR Platform

CompleteⅡ 1st strand cdna Synthesis Kit

Lecture 13: DNA Technology. DNA Sequencing. DNA Sequencing Genetic Markers - RFLPs polymerase chain reaction (PCR) products of biotechnology

Troubleshooting Sequencing Data

ID kit. imegen Anchovies II. and E. japonicus) DNA detection by. User manual. Anchovies species (E. encrasicolus. sequencing.

Gene Expression Assays

Application Note. Biotechnology Explorer Crime Scene Investigator PCR Basics. Kit: A Real-Time PCR Extension

RealStar HBV PCR Kit /2012

Lyme Disease RecA gene. genesig Advanced Kit. DNA testing. Everything... Everyone... Everywhere tests. Primerdesign Ltd.

SYBR Green Realtime PCR Master Mix -Plus-

Speed Matters - Fast ways from template to result

DNA Sequence Analysis

Fluorescent dyes for use with the

Mir-X mirna First-Strand Synthesis Kit User Manual

User Manual/Hand book. qpcr mirna Arrays ABM catalog # MA003 (human) and MA004 (mouse)

Technical Note. Roche Applied Science. No. LC 18/2004. Assay Formats for Use in Real-Time PCR

Supplemental Material. Methods

mircute mirna qpcr Detection Kit (SYBR Green)

RT 2 Profiler PCR Array: Web-Based Data Analysis Tutorial

DNA Integrity Number (DIN) For the Assessment of Genomic DNA Samples in Real-Time Quantitative PCR (qpcr) Experiments

First Strand cdna Synthesis

Factors Influencing Multiplex Real-Time PCR

RT-PCR: Two-Step Protocol

Protocol. Introduction to TaqMan and SYBR Green Chemistries for Real-Time PCR

Eco TM 48 Real Time PCR System. Fastest block-based qpcr. Four colour multiplexing. Supports all chemistries. Fast cycling protocols

Absolute Quantification Getting Started Guide

IIID 14. Biotechnology in Fish Disease Diagnostics: Application of the Polymerase Chain Reaction (PCR)

PrimePCR Assay Validation Report

TaqMan Fast Advanced Master Mix. Protocol

MystiCq microrna cdna Synthesis Mix Catalog Number MIRRT Storage Temperature 20 C

Objectives: Vocabulary:

Gene Mapping Techniques

Human Herpes Virus 4 (Epstein Barr)

Quantification of Hepatitis B Virus. Core Protein Region. 150 tests

Stratagene QPCR Mouse Reference Total RNA

Recombinant DNA & Genetic Engineering. Tools for Genetic Manipulation

All-in-One mirna qrt-pcr Detection System Handbook

Highly specific and sensitive quantitation

DyNAmo cdna Synthesis Kit for qrt-pcr

Evalution the multiplexed analysis of biomarkers made fast and simple by MyCartis

1. Molecular computation uses molecules to represent information and molecular processes to implement information processing.

DNA SEQUENCING SANGER: TECHNICALS SOLUTIONS GUIDE

Data Analysis on the ABI PRISM 7700 Sequence Detection System: Setting Baselines and Thresholds. Overview. Data Analysis Tutorial

Forensic DNA Testing Terminology

qstar mirna qpcr Detection System

User Manual. Reference Gene Panel Mouse Probe protocol. Version 1.1 August 2014 For use in quantitative real-time PCR

RT rxns. RT rxns TRANSCRIPTME Enzyme Mix (1) 40 µl 2 x 50 µl 5 x 40 µl

PyroPhage 3173 DNA Polymerase, Exonuclease Minus (Exo-)

Table of Contents. I. Description II. Kit Components III. Storage IV. 1st Strand cdna Synthesis Reaction... 3

HISTO SPOT SSO System. The most convenient automated HLA typing system. BAG Health Care the experts for HLA and blood group diagnostics

Path-ID Multiplex One-Step RT-PCR Kit

CCR Biology - Chapter 9 Practice Test - Summer 2012

Global MicroRNA Amplification Kit

HBV Quantitative Real Time PCR Kit

Plexor Systems Instrument Setup and Data Analysis for the Applied Biosystems 7300 and 7500 Real-Time PCR Systems

Annex to the Accreditation Certificate D-PL according to DIN EN ISO/IEC 17025:2005

How is genome sequencing done?

Genetic Analysis. Phenotype analysis: biological-biochemical analysis. Genotype analysis: molecular and physical analysis

Amazing DNA facts. Hands-on DNA: A Question of Taste Amazing facts and quiz questions

PrimeSTAR HS DNA Polymerase

Lyme Disease. RecA gene. 150 tests. Quantification of Lyme Disease genomes. Advanced kit handbook HB

TITRATION OF raav (VG) USING QUANTITATIVE REAL TIME PCR

Methods and Application Guide. Introduction to Quantitative PCR

DNA PROFILING IN FORENSIC SCIENCE

Application Guide... 2

Applications Guide. Real-Time PCR Applications Guide

User Manual Mouse Endogenous Control Gene Panel

Mir-X mirna First-Strand Synthesis and SYBR qrt-pcr

HISTO SPOT SSO System

Transcription:

Beginner s Guide to Real-Time PCR

02 Real-time PCR basic principles PCR or the Polymerase Chain Reaction has become the cornerstone of modern molecular biology the world over. Real-time PCR is an advanced form of the Polymerase Chain Reaction that maximizes the potential of the technique. To understand real time PCR it is easier to begin with the principles of a basic PCR: PCR is a technique for amplifying DNA. There are 2 reasons why you may want to amplify DNA. Firstly you may want to simply create multiple copies of a rare piece of DNA. For example a forensic scientist may want to amplify a tiny piece of DNA from a crime scene. More commonly however you may wish to compare 2 different samples of DNA to see which is the more abundant. DNA analysis requires amplification in order for there to be enough DNA to give a detectable signal for quantification. If you amplify both samples at the same rate, you can calculate which sample had the highest copy number of the target of interest to begin with. During a PCR, changes in temperature are used to control the activity of the polymerase and the binding of primers. To begin the reaction the temperature is raised to 95 C. At this temperature all double stranded DNA is melted in to single strands: The temperature is then lowered to ~60 C. This allows the primers to bind to your gene of interest: It is a thermostable polymerase enzyme that drives a PCR. A polymerase will synthesize a complementary sequence of bases to any single strand of DNA providing it has a double stranded starting point. This is very useful because you can choose which gene you wish the polymerase to amplify in a mixed DNA sample by adding small pieces of DNA complimentary to your gene of interest. These small pieces of DNA are known as primers because they prime the DNA sample ready for the polymerase to bind and begin copying the gene of interest.

3 03 Thus the polymerase has somewhere to bind and can begin to copy the DNA strand: The optimal temperature for the polymerase to operate is 72 C so at this point the temperature is sometimes raised to 72 C to allow the enzyme to work faster. There are now twice as many copies of your gene of interest as when you started: This temperature change is repeated through around 40 cycles. Thus one copy becomes 2, 2 become 4, 4 become 8, and so on until billions of copies are created. After amplifying your gene it is possible to run the amplified DNA out on an agarose gel and stain it with a dye which makes it visible. The brighter the visible band, the more copies of your target you have created. Real-time PCR This same principle of amplification is employed in realtime PCR. But instead of looking at bands on a gel at the end of the reaction, the process is monitored in realtime. Literally, the reaction is placed in to a real-time PCR machine that watches the reaction occur with a camera or detector. There are a many different techniques that are used to allow the progress of a PCR reaction to be monitored but they all have one thing in common. They all link the amplification of DNA to the generation of fluorescence which can simply be detected with a camera during each PCR cycle. These different techniques are discussed on page 38. Hence, as the number of gene copies increases during the reaction, so the fluorescence increases.

04 4 Real time PCR has many benefits over the old fashioned approach: Firstly it gives you a look in to the reaction. You can literally see which reactions have worked well and which have failed. The efficiency of the reaction can be precisely calculated. There is also no need to run the PCR product out on a gel after the reaction as the melt curve analysis effectively does this for you. The greatest advantage of all however, is that real-time PCR data can be used to perform truly quantitative analysis of gene expression. In comparison, old fashioned PCR was only ever semi-quantitative at best.

5 Kits, reagents and expertise 05 Real-Time PCR is an exceptionally powerful research tool. With the correct kits, reagents and experimental design it is quick and easy to generate high quality meaningful data in no time with real-time PCR. Whether you are an expert or a complete beginner PrimerDesign Ltd can make your life very easy. We are experts and can help you by providing everything you need to generate the very best possible real-time PCR data. What will you need? Precision Reverse Transcription kits High efficiency Reverse Transcription (RT) ensures the ability to detect rare transcripts and obtain the strongest possible Real- Time PCR signals. As a complete solution, the PrimerDesign Reverse Transcription kit contains all of the reagents necessary for the RT step. genorm Reference gene selection kits genorm is a system for selecting the best candidate reference gene for a given experimental scenario. The kit contains range of assays for reference genes and access to the genorm software in qbase+. Custom designed Real-Time PCR assays for any gene in any species PrimerDesign specialise in the custom design and validation of Real-Time PCR primer assays. Simply supply the name or accession number of your target gene of interest and our team will design the best possible Real-Time PCR primers for that unique sequence. Reference gene assays To compliment your custom gene of interest assay, PrimerDesign has a wide range of reference gene assays which can be used as a normalising signal. Precision 2 x Real-Time PCR Mastermix Precision FAST 2 x Real-time PCR Mastermix is an ultra-fast, cost-saving mix for qpcr. The mix is designed for rapid cycling protocols that can dramatically shorten run times. BrightWhite Real-Time PCR plasticware The best possible Real-Time PCR is performed using white, opaque plasticware. BrightWhite plasticware channels all of the fluorescent output from your reaction straight back to the detector. Brighter, better data.

Please feel free to contact us for free advice or technical support. PrimerDesign Ltd The Mill Yard Nursling Street Rownhams Southampton United Kingdom SO16 0AJ Telephone +44 (0)23 8074 8830 Fax +44 (0)870 836 2155 Orders orders@primerdesign.co.uk Enquiries enquiry@primerdesign.co.uk Technical support support@primerdesign.co.uk PrimerDesign works to an ISO 9001:2008 certified quality management system Products for Real-Time PCR