1 QUANTITATIVE PCR Quantitative PCR Systems Our QPCR systems meet your current research needs, offer flexibility for future research goals, and match your budget. HIGH-PERFORMANCE FULL-FEATURED FLEXIBLE Mx3005P System Mx3000P System
2 QUANTITATIVE PCR > Mx FAMILY OF QPCR SYSTEMS Bringing QPCR Systems to Every Lab Real-time quantitative PCR (QPCR) is today s method of choice for quantifying nucleic acids. By monitoring PCR amplification in real-time, it is possible to measure the reaction during the exponential phase of growth, a time when none of the reagents are limiting and the reaction is most efficient. This allows real-time QPCR to achieve more sensitive detection, better reproducibility, and a wider linear dynamic range than conventional methods. Our Mx3000P and Mx3005P QPCR Systems a offer the highest performance and flexibility in QPCR instrumentation at an affordable price. CONTENTS: Mx3000P QPCR System Mx3005P QPCR System MxPro QPCR Software QPCR and QRT-PCR Reagents Fast Track QPCR Education Program QPCR Systems and Reagents Features, Specifications, and Selection Guide Ordering Information
3 QUANTITATIVE PCR > Mx3000P QPCR SYSTEM The First High-Performance, Low-Cost QPCR System With the Mx3000P QPCR System, we were first to offer an affordable system that supported multiple applications. Features of the Mx3000P QPCR System The Mx3000P system is a high-performance, full-featured instrument system designed to accommodate basic experimental design and also offer the flexibility required for more advanced applications. The Mx3000P QPCR System brings real-time instrumentation to the individual researcher with a limited budget. Four optical channels with user-selected filters for greater flexibility Broad wavelength range excitation supports most fluorescent dyes Defined excitation and emission detection wavelengths ideal for superior multiplex results Single photomultiplier tube for detection ensures superior sensitivity and linear dynamic range to ten orders of magnitude (Figures 1 and 2) A B Figure 1 TWO-FOLD DILUTION SERIES Four replicates of a dilution series from 20,000 to 1.2 copy equivalent of plasmid containing ß-actin target detected with a molecular beacon. Average delta Ct between dilutions is 0.95 cycles. Figure 2 TEN ORDERS OF MAGNITUDE DYNAMIC RANGE (A) Eight replicates of ten fold dilutions of plasmid DNA for ß-actin target. (B) Standard curve displayed with 99% confidence intervals and efficiency=98% and Rsq=
4 2>3 QUANTITATIVE PCR > Mx3005P QPCR SYSTEM Superior Flexibility and High Performance Without the Cost The Mx3005P QPCR System advances the proven Mx3000P System. Offering unmatched flexibility and capability, the Mx3005P System can support even more real-time QPCR applications and chemistries to accommodate your research needs now and in the future. Advanced Optical System The Mx3005P System features the same optical scanning design as the Mx3000P system. A scanning fiber optic head ensures all wells 1) receive the same amount of excitation light, 2) are detected for the same amount of time, and 3) are the same distance from the detector. The scanning motion system of the fiber optic cable eliminates optical variation based on well position in the 96-well block, thus eliminating the need for signal correction by calibration or reference dyes. The photo- multiplier tube (PMT) has a large dynamic range of detection and a low signal to noise ratio, allowing low- to high-abundance targets to be accurately quantified. Excitation light is generated by a halogen lamp and delivered to the sample through fiber optics. The fiber optic bundle is coaxial so it delivers excitation light and simultaneously detects fluorescence emission from the sample. Detected light is delivered to the PMT via the fiber optic cable (Figure 3). Figure 3 OPTICAL SYSTEM DESIGN The halogen lamp in the instrument systems provides a wide-range of excitation allowing more dye flexibility with more intensity than standard light emitting diodes (LEDs). The excitation and emission filters are defined to narrow wavelengths to minimize fluorescence signal crosstalk. Fiber optic bundles channel the light into the plate and back to the PMT to ensure minimal signal loss. Figure 4 96-WELL UNIFORMITY SYBR Green I uniformity assay for ß-actin containing plasmid. Average Ct value at threshold is 18.1 and standard deviation of Ct values is Ct range across 96 wells is 0.26 cycles (18.00 to 18.26).
5 Mx3005P Optical Filters The new five-position customizable filter wheel design offers a multitude of dye choices, multiplex dye combinations enabling up to five targets per well, and the ability to detect fluorescence resonance energy transfer (FRET) signals. You can choose which five filters are installed in the instrument from a list of eight filter sets spanning deep blue dyes to far red dyes thus maximizing the useable wavelength spectrum (Table 3). Precision Thermal System The thermal system of the Mx3005P system shares the same Peltier-based design with the Mx3000P system. This system ensures uniform ramping and thermal accuracy for amplification reproducibility from well-to-well and run-to-run (Figure 4). Powerful Data Analysis Software The Mx3005P system uses the most advanced version of our graphical user interface and data analysis software. The MxPro QPCR Software is easy to use and organized by application so you can easily navigate the software and run assays quickly. Five optical channels with user-selected filters for greater flexibility Defined excitation and emission detection wavelengths are ideal for superior multiplex results, up to five targets simultaneously (Figure 5) Custom filter path selection to support FRET signal detection Open platform design supports all fluorescent chemistries and numerous applications (Figure 6) Mx3005P QPCR System Figure 5 5-PLEX STANDARD CURVES Three replicates of 4-fold dilutions of QPCR Human Universal Reference cdna detecting five gene targets simultaneously. Detection from the highest abundance to the lowest abundance gene target (CYCLO to ENOS gene targets) spans a Ct range of (delta Ct = 20). Figure 6 RNA QUANTIFICATION BY RIBOGREEN PLATE READ EXPERIMENT Three replicates of RNA standards from 500 pg to 5 ng. Standard curve generated from plate read experiment automatically quantitates RNA concentration in unknown samples. Ideal for quick and accurate quantification of RNA samples before performing gene expression QPCR experiments.
6 4>5 QUANTITATIVE PCR > MxPro QPCR SOFTWARE Novel Data Analysis in the Easiestto-Operate QPCR Software Available The MxPro QPCR Software for the Mx3000P and Mx3005P Systems combines cutting-edge data analysis algorithms with intuitive organization designed for ultimate ease-of-use. Setting Up and Running the Experiment The experimental setup features well definition by target assay name (e.g., FAM = p53), automated standard curve setup, customized well naming, importing plates, and a flexible thermal profile setup to accommodate any thermal cycling programming (Figure 7). During the run, you can view your QPCR data in 96 individual wells or as a consolidated view on a single screen. In addition, the internal storage memory of the Mx3000P and Mx3005P systems allows you to analyze the data during a run in a standalone application while the instrument-connected application continues to collect data. Data Analysis and Reporting the Results The data analysis module includes two automated methods for baseline subtraction and threshold setting, both of which can be customized for any particular application. The MxPro QPCR software Adaptive Baseline algorithm dynamically assigns baseline start and end cycles for all amplification plots independently. This ensures optimal baseline correction and increases the reliability of accurately detecting high and low template concentrations in the same assay and analyze multiple assays simultaneously (Figure 8). The Comparative Quantification module automatically determines gene expression fold change, calculates statistical error, and generates a publication quality chart (Figure 9). After analysis, the MxPro QPCR Software is capable of creating custom reports and exporting all plots, charts, and tables (Figure 10). Images can be directly exported to Microsoft PowerPoint, and highresolution bitmap images, Chart and plot data can be exported to Microsoft Excel,.xml, and.txt formats to easily re-create the data in different formats (Figure 11). All text data can also be exported in any of these formats. Intuitive organization and easy-to-use View and analyze data in real-time Multiple customizable data analysis algorithms for baseline correction and threshold setting Export images directly from the software, export the raw data to re-create the image, and export the text data in multiple formats Figure 7 FLEXIBLE, EASY TO USE PLATE SETUP Import Plate Setup from previous experiments or templates. Assign assay/gene target names to dyes. Setup standard curve and replicates using auto-increment feature. Add well information to identify sample name, number, quantity, or any other sample specific information. Figure 8 MULTIPLE DATA ANALYSIS VIEWS View data in multiple formats. Amplification plot and standard curve data can be displayed simultaneously and changes in threshold are instantly displayed on the standard curve. The Adaptive Baseline algorithm ensures accurate quantification across all five gene targets.
7 Figure 9 AUTOMATED ANALYSIS OF GENE EXPRESSION DATA The Comparative Quantitation module in MxPro Software automatically calculates relative quantity for gene expression experiments. Data is displayed as normalized fold gene expression to a reference control on a log(2) scale with upper and lower error limits based on variation in the replicates. In the figure above, fold expression change for six genes across two treatments is displayed. Figure 10 CREATE CUSTOM DATA REPORTS Create a custom data report by determining report format and which data sets to display. In the figure above, Plate Setup, Thermal Profile, Amplification Plots, Standard Curve, and Text Report are selected for the report. Figure 11 EXPORT DATA IN MULTIPLE FORMATS Export any data set directly from the MxPro Software in.xls,.ppt,.bmp,.txt, or.xml format. Charts and graphs can be exported directly to Microsoft PowerPoint and Excel. Exporting to Excel automatically generates a data table and the chart.
8 6>7 QUANTITATIVE PCR > QPCR AND QRT-PCR REAGENTS Brilliant and FullVelocity QPCR and QRT-PCR Reagents We offer two families of QPCR and QRT-PCR reagents, Brilliant and FullVelocity master mixes. Each uses a different PCR enzyme formulation to provide efficient, reproducible quantification using probe-based or SYBR Green detection chemistries. Brilliant QPCR and QRT-PCR Master Mixes b,c Brilliant QPCR Reagents provide high sensitivity and broad dynamic range required for real-time PCR analysis. Brilliant QPCR Master Mixes utilize SureStart Taq DNA polymerase b for high specificity, and StrataScript Reverse Transcriptase d provides superior real-time QPCR sensitivity compared to RNase H(+) reverse transcriptases. Brilliant SideStep QPCR and QRT-PCR Master Mixes Combining our SideStep Lysis and Stabilization Buffer e with our Brilliant QPCR and QRT-PCR master mixes allows you to use cell lysates directly in a real-time QPCR amplification skipping RNA purification steps. This method prevents sample loss and degradation, ensuring accurate gene quantification in downstream QRT-PCR. SideStep cell lysates can be stored for up to 6 months before QRT-PCR analysis. FullVelocity QPCR and QRT-PCR Reagents b FullVelocity QPCR Master Mixes provide a fast and economical system for real-time QPCR applications. FullVelocity master mix results are produced 30 to 50% faster than traditional Taq-based methods. Key to the FullVelocity technology is the unique high-speed archaeal DNA polymerase engineered to excel in rapid, two-step cycling conditions. FullVelocity SYBR Green master mixes are economical and formulated with two specificity enhancers for high specificity during every cycle. For a complete list of our QPCR and QRT-PCR reagents, see Table 1. REAL-TIME QPCR REAGENTS GUIDE PROBE-BASED DETECTION SYBR GREEN DETECTION Format DNA (cdna) Quantification RNA Quantification RNA Quantification DNA (cdna) Format Quantification 1-Step 2-Step 1-Step 2-Step Master Mix Brilliant QPCR Master Mix (up to 2 targets) or Brilliant Multiplex QPCR Master Mix (up to 4 targets) Brilliant QRT-PCR Master Mix, 1-Step Brilliant QRT-PCR Master Mix, 2-Step Master Mix Brilliant SYBR Green QPCR Master Mix Brilliant SYBR Green QRT-PCR Master Mix, 1-Step Brilliant SYBR Green QRT-PCR Master Mix, 2-Step Core Reagent Kit (Standard dntps) Brilliant QPCR Core Reagent Kit Brilliant QRT-PCR Core Reagent Kit, 1-Step Stratascript QPCR cdna Synthesis Kit plus Brilliant QPCR Core Reagent Kit Master Mix FullVelocity SYBR Green QPCR Master Mix FullVelocity SYBR Green QRT-PCR Master Mix, 1-Step FullVelocity SYBR Green QRT-PCR Master Mix, 2-Step Core Reagent Kit (dutp and/or UNG) Brilliant QPCR Plus Core Reagent Kit Brilliant QRT-PCR Plus Core Reagent Kit, 1-Step Brilliant QRT-PCR Plus Core Reagent Kit, 2-Step Core Reagent Kit (Standard dntps) Brilliant SYBR Green Core Reagent Kit StrataScript QPCR cdna Synthesis Kit plus Brilliant SYBR Green Core Reagent Kit Table 1 CHOOSE THE RIGHT MASTER MIX OR CORE REAGENT DEPENDING ON YOUR APPLICATION.
9 QUANTITATIVE PCR > FAST TRACK QPCR EDUCATION PROGRAM Rapid and Effective QPCR Education On-Demand The Fast Track QPCR Education Program is a comprehensive program of training and advanced education for users of our QPCR instruments. Getting Started with QPCR Our Introduction to QPCR Guide provides you with a review of the technology and in-depth details on experimental design, assay setup, assay optimization, and data analysis. This guide walks you through a QPCR experiment from start to finish and includes some advanced methods for optimization, troubleshooting, and alternative approaches to quantification. The Fast Track QPCR Education Program provides a wide range of tools to get you up and running with QPCR quickly and effectively. We offer a wide selection of web seminars, updated Technical and Application Notes, a comprehensive Introduction to QPCR Guide, and regularly scheduled Regional QPCR User Group Meetings. The program also offers you access to expert Field Application Scientists providing advanced education. The Fast Track QPCR web seminars can be found at The web seminars can be viewed in real-time or you can download the recorded version and pdf version of the PowerPoint slides. The list of current Fast Track QPCR Seminars includes: Principles of Quantification in QPCR QPCR Assay Design Analysis QPCR Primer and Probe Design QPCR Assay Controls QPCR Assay Validation and Optimization QPCR Data Analysis MxPro QPCR Software: Basic Functionality MxPro QPCR Software: Advanced Functionality To download our Introduction to Quantitative PCR: Methods and Application Guide, review our updated web seminars, or check for the next Regional QPCR User Group Meeting in your area, visit
10 8>9 QUANTITATIVE PCR > QPCR SYSTEMS AND REAGENTS FEATURES, SPECIFICATIONS, AND SELECTION GUIDE Table 2 Mx3000P AND Mx3005P FEATURES AND SPECIFICATIONS Table 3 Mx3000P and Mx3005P SYSTEM FILTER CHOICES SAMPLE CAPACITY Standard 96-well plates, 0.2 ml 8-strip tubes or individual tubes FILTER SETS EXCITATION WAVELENGTHS / EMISSION WAVELENGTHS DIMENSIONS AND WEIGHT 33 cm W x 46 cm D x 43 cm H and 20 kg ALEXA Fluor nm / 440 nm SAMPLE VOLUME µl FLUORESCENCE EXCITATION FLUORESCENCE DETECTION Quartz tungsten-halogen lamp, nm range Single photomultiplier tube (PMT), nm range FILTERS AVAILABLE Alexa Fluor 350, FAM /SYBR Green I, TET, HEX /JOE /VIC, Cy 3, TAMRA, ROX /Texas Red, Cy 5 FAM /SYBR Green I TET HEX /JOE /VIC Cy nm / 516 nm 517 nm / 538 nm 535 nm / 555 nm 545 nm / 568 nm NUMBER OF OPTICAL CHANNELS Four (Mx3000P System) or five (Mx3005P System) user-selected excitation/emission filter sets TAMRA 556 nm / 580 nm OPTICAL FILTER MOVEMENT Simultaneous matched movement of excitation and emission filters; Mx3005P System capable of custom filter alignment (e.g., mismatch excitation and emission filters: FAM excitation / ROX emission) ROX /Texas Red Cy nm / 610 nm 635 nm / 665 nm OPTICAL MEASUREMENTS Fiberoptic scanning head takes measurements at any single plateau or multiple plateaus THERMAL UNIFORMITY +/ C within 12 seconds at 72 C THERMAL BLOCK RAMP RATE TYPICAL RUN TIME MULTI-INSTRUMENT CONTROL MULTIPLEX Up to 2.5 C/second Standard 40 cycle 2-step QPCR reaction completed in 90 minutes; the same reaction is completed in 60 minutes using FullVelocity reagents (plus dissociation curve) Up to 6 instruments simultaneously from one computer Up to 4 targets (Mx3000P System) or five targets (Mx3005P System) simultaneously CHEMISTRIES SUPPORTED SYBR Green I, Taqman, molecular beacons, Eclipse probes, Scorpion primers, Lux primers, and Plexor system Table 4 QPCR SYSTEMS AND REAGENTS SELECTION GUIDE APPLICATION PRODUCT ADVANTAGES Single-color to five-color multiplex, 96-well format with powerful data analysis software Mx3000P or Mx3005P QPCR System + Four or five optical channels with user-selected filters for greater flexibility + Broad wavelength range excitation supports most fluorescent dyes + Defined excitation and emission detection wavelengths are ideal for superior multiplex results + Open platform design supports all fluorescent chemistries High-throughput single-color to five-color multiplex, 96-well x 2 format (192 wells) with powerful data analysis software Mx3000P Duet QPCR System or Mx3005P Duet QPCR System + Run two Mx3000P or Mx3005P QPCR Systems from a single computer + Ideal for higher throughput labs on a budget + Capable of running up to 6 systems from a single computer simultaneously Multiple instruments with singlecolor to five-color multiplex on a budget with powerful data analysis software Mx3000P / Mx3005P Combo QPCR System + Run one Mx3000P system and one Mx3005P system from a single computer simultaneously + Ideal for larger labs and core labs requiring a flexible platform to support research applications in the future Real-time QPCR with significantly shorter run times (DNA, cdna, and RNA targets) FullVelocity QPCR and QRT-PCR Master Mixes + Sensitive one-step QRT-PCR in less time + High speed enzyme supports rapid cycling conditions + Increase throughput Pre-optimized for sensitive and reproducible real-time quantification (DNA, cdna, and RNA targets) Brilliant QPCR and QRT-PCR Master Mixes + Made with optimized buffers and performance tested for reproducible results up to 24 months + Master mix format reduces pipetting steps and minimizes user error + dutp in nucleotide mixes so UNG can be added for carryover contamination control
11 Ordering Information PRODUCT QUANTITY / FORMAT CATALOG NO. QPCR Systems Mx3000P QPCR System 4-color system (110v) with notebook computer color system (110v) with desktop computer color system (230v) with notebook computer color system (230v) with desktop computer Mx3005P QPCR System 5-color system (110v) with desktop computer color system (110v) with notebook computer color system (230v) with desktop computer color system (230v) with notebook computer QPCR and QRT-PCR Reagents Brilliant QPCR Master Mix Kits SYBR Green-based detection, 400 rxn x 25 µl Probe-based detection, 400 rxn x 25 µl Brilliant QRT-PCR Master Mix Kits, 1-step SYBR Green-based detection, 400 rxn x 25 µl Probe-based detection, 400 rxn x 25 µl Brilliant QRT-PCR Master Mix, 2-Step Probe-based detection, 400 rxn x 25 µl Brilliant SYBR Green QRT-PCR Master Mix, 2-Step SYBR Green-based detection, 400 rxn x 25 µl Brilliant SYBR Green SideStep QPCR Master Mix SYBR Green-based detection, 400 rxn x 25 µl Brilliant SideStep QRT-PCR Master Mix, 1-step SYBR Green-based detection, 400 rxn x 25 µl Brilliant SYBR Green SideStep QRT-PCR Master Mix, 2-Step SYBR Green-based detection, 400 rxn x 25 µl FullVelocity SYBR Green QPCR Master Mix Kits SYBR Green-based detection, 400 rxn x 25 µl FullVelocity SYBR Green QRT-PCR Master Mix Kits, 1-step SYBR Green-based detection, 400 rxn x 25 µl FullVelocity SYBR Green QRT-PCR Master Mix, 2-Step SYBR Green-based detection, 400 rxn x 25 µl StrataScript QPCR cdna Synthesis Kit 2-step QRT-PCR, 50 rxn LEGAL LANGUAGE Mx3000P, Brilliant and StrataScript are registered trademarks of Stratagene in the United States. Mx3005P, MxPro, and FullVelocity are trademarks of Stratagene in the United States. ALEXA Flour 350 is a registered trademark of Molecular Probes. Microsoft, Excel and PowerPoint are registered trademarks of Microsoft. SYBR is a registered trademark of Molecular Probes. FAM, TET, HEX, VIC, JOE, TAMRA, and ROX are trademarks of Applera Corporation or it s subsidiaries in the US and certain other countries. Cy 3 and Cy 5 are trademarks of Amersham Biosciences. RiboGreen is a registered trademark of Molecular Probes. TaqMan is a registered trademark of Roche Molecular Systems, Inc. Beacon Designer is a trademark of PREMIER Biosoft International a. This instrument is an Authorized Thermal Cycler. Its purchase price includes the up-front fee component of a license under the non-u.s. counterparts of United States Patent Nos. 4,683,195, 4,683,202 and 4,965,188 owned by F. Hoffmann-La Roche Ltd, covering the Polymerase Chain Reaction ( PCR ) process, to practice the PCR process for internal research and development using this instrument. The running royalty component of that license may be purchased from Applied Biosystems or obtained by purchasing Authorized Reagents. This instrument is also an Authorized Thermal Cycler for use with applications licenses available from Applied Biosystems. Its use with Authorized Reagents also provides a limited PCR license in accordance with the label rights accompanying such reagents. Purchase of this product does not itself convey to the purchaser a complete license or right to perform the PCR process. Further information on purchasing licenses to practice the PCR process may be obtained by contacting the Director of Licensing at Applied Biosystems, 850 Lincoln Centre Drive, Foster City, California 94404, USA. No rights are conveyed expressly, by implication or estoppel to any patents on real-time methods, including but not limited to 5 nuclease assays, or to any patent claiming a reagent or kit. Applied Biosystems does not guarantee the performance of this instrument. b. Purchase of this product is accompanied by a license under the foreign counterparts of U.S. Patents Nos. 4,683,202, 4,683,195 and 4,965,188 for use in the polymerase chain reaction (PCR) process, where such process is covered by patents, in conjunction with a thermal cycler whose use in the automated performance of the PCR process is covered by the up-front license fee, either by payment to Applied Biosystems or as purchased, i.e., an authorized thermal cycler. c. Use of labeling reagents may require licenses from entities other than Stratagene. For example, use of fluorogenic probes in 5' nuclease assays may require licenses under U.S. Patent Nos. 6,214,979, 5,804,375, 5,210,015 and 5,487,972 owned by Roche Molecular Systems, Inc. and under U.S. Patent No. 5,538,848 owned by Applied Biosystems. TaqMan is a registered trademark of Roche Molecular Systems, Inc. d. Purchase of this PCR-related product does not convey any rights under the foreign counterparts of the PCR patents owned by Roche Molecular Systems. A license to use the PCR process, where such process is covered by patents, accompanies the purchase of certain reagents from Stratagene when used in conjunction with an Authorized Thermal Cycler. e. Patents pending.
12 AMPLIFICATION CELL BIOLOGY CLONING MICROARRAYS NUCLEIC ACID ANALYSIS PROTEIN FUNCTION & ANALYSIS QUANTITATIVE PCR SOFTWARE SOLUTIONS Stratagene USA and Canada Order: x3 Technical Services: x2 Stratagene Europe Order: Technical Services: Stratagene Japan K.K. Order: Technical Services: Distributors > For a list of worldwide distributors, please visit our website North Torrey Pines Road La Jolla, CA USA BR65
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Real-time quantitative RT -PCR (Taqman) Author: SC, Patti Lab, 3/03 This is performed as a 2-step reaction: 1. cdna synthesis from DNase 1-treated total RNA 2. PCR 1. cdna synthesis (Advantage RT-for-PCR
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