TATAA Interplate Calibrator User Manual
Contents
1. of the IPC is measured with high accuracy The TATAA IPC has been extensively optimized to reliably and predictably amplify providing highly reproducible C values However it is still recommended as good practice to run technical replicates of the TATAA IPC preferably at least triplicates Figure 2 Poor assays should never be used as interplate calibrators since the noise contributed by these measurements may in turn worsen the quality of the data rather than improving it It is sufficient to run one set of IPC replicates for each instrument channel used within a study if a common threshold is set Hence for most singleplex assay technical replicates of a single IPC are sufficient It is not recommended to perform separate inter plate calibrations for each assay since the noise contributed by the independent corrections is likely to reduce data quality IPC assay 0 3 Rotorgene 72 Viia7 384 0 2 LC480 384 2nd derivative LC480 384 fit points D 0 1 kai Yo number of qPCR replicates 0 0 Figure 2 The relationship between the standard error of the mean SEM and the number of replicates used in runs with identical set tings except for their being processed on different instruments see fig ure legend LC480 shows two different threshold settings on one run TATAA Interplate calibrator is e provided in aliquots stored at 20 C for easy and flexible use and long term stability e a robust2. your assays Often 60 C annealing temperature is used on three two step SYBR protocols and qPCR conditions that have been vali dated for the TATAA Interplate Calibrator are shown in Table 1 The ampli con produced by the TATAA IPC assay is 100 bp long 4 Inspect data The amplification curves of the TATAA Interplate Calibra tor IPC assay should be parallel with those of your assays at least up to threshold if it is not see section additional information Collect the C values for all the runs and average those of the IPC replicates in each run The standard deviation SD of IPC replicates should be lt 0 3 cycles and usually it is substantially lower the reproducibility is usually limited by the performance of your qPCR instrument Data are corrected for the varia tion between runs using the equation TATAA Interplate Calibrator SYBR no plates gt Cq IPC i i l no plates E corrected uncorrected IPC 1 Cq Cq C For each plate subtract the cy from the measured cgp aran and add the no plates Fa He average of the C s off all IPCs _ hi no plates E For convenient analysis interplate calibration is part of the qPCR data analysis workflow in softwares such as GenEx GenEx To enable automatic analysis runs and interplate calibrators should be indexed in classification columns It is easy to do this manually however if you use pre plated reactions by leading vendors GenEx will aut
3. User Manual TATAA Interplate Calibrator SYBR protocol 250 1000 rxn Version 1 1 August 2012 For use in quantitative real time PCR Q tataabiocenter Table of contents Background i ocmmmnmmnnnnnmnnnnnnnnnnnnnnnnnnnnnnnununununnnnnnnnnnn Contents sss Additionally required materials and OVC rap au oes tse eed ay tote asses tesa et Storage Interplate calibration additional information Protocol Interplate calibration 00 GENEX An Troubleshooting References nnn Reorder information Contact Licenselinformationits ea a a Other products from TATAA qPCR training courses at TATAA Biocenter ee TATAA Interplate Calibrator SYBR 13 veel 1S Background For practical reasons many qPCR studies involve the use of samples that are processed in more than a single batch or in which the sample set is extended over time Even over a short time period variation between qPCR processing runs is observed due to different baseline subtractions and threshold settings The bias is NOT introduced when using the all samples or all assays plate layout and performing AAC based analysis but it is the mixed layout for which interplate calibration is needed Figure 1 The TATAA Interplate Calibrator IPC is used to compensate for the variation between qPCR runs The TATAA IPC sample material is provided in ready to use aliquots and is a very stable template that is amplified with a hig
4. an of the control sample TATAA Universal Spikes have a synthetic sequence that is not present in any known living organism The Spike assay is exceedingly robust and is optimized for high sensitivity for inhibition The E of the Spike assay also reflects losses during extraction handling transport and storage of samples including freeze thaw events during RT qPCR ValidPrime mouse human and other vertebrates ValidPrime is an assay to test for the presence of gDNA in test samples and when combined with a gDNA control sample replaces all RT controls Valid Prime is highly optimized and specific to a non transcribed locus of gDNA that is present in exactly one copy per haploid normal genome The kit also contains a gDNA standard that can be used to test the sensitivity of RT qPCR assays for gDNA background ValidPrime replaces the need to perform RT controls for all reactions and makes RT qPCR profiling easier and substantially cheaper HL dsDNase New generation DNase from Arcticzymes that is specific to double strand DNA and can be efficiently inactivated by heating at 55 C It can be added to your RT reaction to efficiently remove any gDNA without degrading single stranded cDNA It is completely inactivated by the PCR and does not degrade the double stranded PCR product GenEx software Market leading software for qPCR analysis from MultiD Analyses GenEx pro vides the appropriate tools to analyze qPCR gene expressio
5. assay that performs excellent in most master mixes and over a wide range of annealing temperatures a stable template at optimum concentration that produces C 10 15 under most conditions Contents e Interplate Calibrator IPC template 50 aliquots 20 ul c 10 copies pl or 200 aliquots 20 ul c 10 copies ul e IPC primers 5 aliquots 50 rxns 250 ul of primer mix c 2 uM per primer or 20 aliquots 50 rxns 1000 ul of primer mix c 2 uM per primer rxns qPCR reaction in 25 ul concentration 400nM per primer The IPC assay produces a 100 bp amplicon with very high PCR efficiency E gt 90 in tested commercial master mixes and produces negligible primer dimer products Additionally required materials and devices Real time PCR instrumentation The TATAA Interplate Calibrator has been validated on the Roche LightCycler 480 Biorad CFX 96 384 Stratagene MxPro Rotorgene ABI 7500 Fast Eppen dorf Realplex Illumina Eco Fluidigm BioMark and is expected to perform well on equivalent instruments e Master mix The TATAA Interplate Calibrator assay has been validated in a large number of master mixes using conditions recommended by the manufacturers Table 1 Master mix Final concentrations TATAA Interplate Calibrator SYBR Annealing temperature Applied Biosystems Fast SYBR Green Master Mix 400 nM primer 60 C 60 65 Biorad iQ SYBR Green Supermi
6. enEx Data Analysis Software In qPCR in Applied Microbiology Editor Martin Filion Horizon Press 2012 Tichopad A Svec D Pfaffl M Kubista M How good is a PCR efficiency estimate Proposal of recommendations for precise and robust qPCR efficiency estimation NucleicAcidResearch 2012 GenEx user guide http www tataa com files pdf GenExUserGuide pdf Reorder information The TATAA Interplate Calibrator can be ordered from the TATAA webshop on www tataa com or by mail order tataa com or from the TATAA distributor in your country Contact For more information about TATAA Interplate Calibrator contact us at info tataa com License information PCR is covered by several patents owned by Hoffman La Roche Inc and Hoffman LaRoche Ltd Purchase of this kit does not include or provide a license with respect to any PCR related patents owned by Hoffman La Roche or others TATAA Biocenter does not encourage or support the unauthorised or unlicensed use of the PCR process 13 14 Other products from TATAA Universal RNA DNA spike for any species tests for inhibition and yield The TATAA Universal Spike is an easy to use and very effective tool for qual ity control throughout entire RT qPCR experimental workflow Add the spike to the experimental sample and to a control based on water Processing both samples exactly the same way any inhibition in the experimental sample will impair the RT qPCR resulting in higher C th
7. hly robust assay The TATAA IPC should be included in all qPCR runs Any differences in the measured IPC C values among the runs reflect the bias introduced by the instrument and is compensated for RSS i 53 Figure 1 Different options for the design of a multi plate qPCR study for AAC based analysis Top left the study contains 24 samples and 16 genes and requires four runs with 96 well block instruments y axis samples x axis genes Top right All samples are always assayed on the same plate Bottom left All genes are always assayed on the same plate Bottom right Mixed design which requires interplate calibration The TATAA IPC is also suited for absolute quantification The recommended strategy is to construct a single highly precise standard curve for your target gene Base it on large number of standards covering a wide concentration range TATAA Interplate Calibrator SYBR recommended 7 9 concentrations each run in 3 4 replicates This standard curve is then used for interpolation of all field samples The field samples may be measured over time in independent runs Proper interpolation then requires that the IPC sample is included in each run This approach is much more accurate than running a separate standard curve in each run particularly if based ona smaller number of standards since the random noise in the separate standard curves introduces systematic run to run variation Tichopad 2012 The C
8. n data and to ex tract biologically relevant information from the measurements TATAA Interplate Calibrator SYBR Reference Gene Panel Human Mouse or Rat The panel contains primer sets for 12 commonly used human mouse or rat ref erence genes A perfect product for finding the most optimal reference genes for your study A one year license for GenEx Standard software with geNorm and Normfinder is included with the kit VisiBlue qPCR mix colorant The VisiBlue mastermix colorant enables you to color your favourite qPCR mas ter mix to easily visualize where the reagent is loaded to your plates and tubes VisiBlue is very easy to use by simple addition to your favorite master mix CelluLyser for rapid and easy lysis and cDNA synthesis The CelluLyser Lysis and cDNA Synthesis Kit enables you to generate cDNA from small samples with minimal losses and hands on time It is particularly useful for single cell analysis By using CelluLyser the entire workflow from cell lysis to RT and qPCR can be performed without washing steps thus elimi nating material loss TATAA GrandMaster and GrandScript Series After specializing in qPCR for more than a decade TATAA Biocenter now intro duces its own series of mixes and cDNA synthesis kits for optimal and high quality results Our mission is to deliver a reagent series that provides superior qPCR per formances ina variety of applications and throughout the entire qPCR workflow qPCR t
9. ntact us at info tataa com e My replicates are not tight With TATAA Interplate Calibrator template and primers and good pipetting technique high reproducibility is expected SD lt 0 3 C in all master mixes SD lt 0 5 cycles can still be accepted but the number of replicates should be increased for accurate interplate calibration If other assays show such a low re producibility it is possible that the qPCR instrument is not performing well and should be validated test for uniformity of the thermal block Low amounts of template can lead to higher variation Also low quality RNA DNA can lead to differences between replicates Check the accuracy and reproducibility of your pipettes e My negative controls are amplified Your reagents are probably contaminated e My samples have same higher C value than my NTC You have used too little template or complete inhibition is present Add more RNA DNA and try again Check if the quality of the RNA DNA is not com promised due to improper storage before performing RT qPCR Check if the instrument is set optimally TATAA Interplate Calibrator SYBR References Bustin SA Benes V Garson JA Hellemans J Huggett J Kubista M Mueller R Nolan T Pfaffl MW Shipley GL Vandesompele J Wittwer CT The MIQE guidelines minimum information for publication of quantitative real time PCR experiments Clin Chem 2009 Apr 55 4 61 1 22 Kubista M Rusnakova V Svec D Sj green B Tichopad A G
10. omatically identify interplate calibrators and annotate your experiment accordingly A free license for GenEx Enterprise is available for download from www multid se and provides the fully functional analysis software for a trial period of 30 days To purchase GenEx licenses or for qPCR data analysis services contact us at order tataa com GenEx is market leading software for qPCR experimental design and data processing and is supported by all leading qPCR instrument manufacturers It offers user friendly optimized workflows for qPCR data pre processing and analysis including normalization using spikes and identification of inhibited outliers Pre processing includes interplate calibration efficiency correction various normalization options handling of technical replicates and missing data normalization with paired samples and correction for gDNA contami nation using ValidPrime Analyses include absolute quantification relative quantification and expression profiling Tutorials are available on www multid se tutorials php and free support is offered on www qpcrforum com 11 12 Troubleshooting e do not get any amplification signal The instrument may not have been programmed correctly or there may be a problem with the master mix Establish if the problem is in the detection or the amplification step by running the samples on a gel Run a new test using the IPC template with the IPC assay provided If the problem persists co
11. ormance has been validated within these temperature ranges Pipettes and tips available from www tataa com e Vortex and centrifuge e Experimental sample DNA cDNA Optionally reference cDNA and gDNA New assays can be validated on cDNA and DNA libraries available from TATAA www tataa com for mouse human or rat Storage For long term storage store the TATAA Interplate Calibrator aliquots at 20 C The TATAA IPC is stored in a stabilizing buffer and shows no degradation within a week at room temperature or after four freeze thaw cycles Figures 3 4 The primer mix and probe may be stored at 20 C for up to a year or at 4 C for up to one month Avoid repeated freeze thaw cycles use the provided aliquots instead Time stability of TATAA Interplate Calibrator _ Freeze thaw stability of TATAA Interplate Calibrator e IPC in nuclease free H2O IPC in nuclease free H2O 27 IPC in stabilizing buffer 27 IPC in stabilizing buffer 26 26 25 25 o o o o 24 E ii 24 i ta 23 23 Time in room temperature days Freeze thaw cycles Figure 3 Stability of TATAA Interplate cali Figure 4 Stability of TATAA Interplate cali brator template in time in room tempera brator template after repeated cycles of ture freezing in 80 C and thawing Interplate calibration additional information A basic requirement for a simple and efficient interplate calibration is having parallel amplification cur
12. raining courses at TATAA Biocenter TATAA Biocenter is leading organizer of hands on training in qPCR and related technologies For comprehensive training program see www tataa com TS Express your genius TATAA Biocenter with offices in Gothenburg San Francisco and Prague is the leading provider of real time PCR services and the prime organizer of real time PCR work shops globally TATAA Biocenter con ducts commissioned research and training within the field of molecu Q tataabiocenter lar diagnostics and gene expression analysis along with developing real time PCR expression panels TATAA Biocenter has great experience and expertise in high resolution gene expression profiling pathogen de tection and small sample single cell analysis TATAA Biocenter AB Odinsgatan 28 411 03 G teborg Tel 46 31 761 57 00 Fax 46 31 15 28 90 E mail info tataa com Website www tataa com
13. strument calibration If parts of a qPCR study must be measured on a different instrument not recommended but still using the same protocol the TATAA Interplate Calibrator can be used to remove most of the systematic variation 10 Protocol Interplate calibration 1 Design your experiment and plan where to include the TATAA Interplate Calibrator We recommend running minimum of three qPCR technical replicates of the TATAA IPC in every run Recommendation Putting the IPC in the same position on the plate in every run makes analysis more convenient uniformity should not be a problem on a well calibrated qPCR instrument 2 Use in house PCR reagents and recommended primer concentration for qPCR Add 2 ul of TATAA Interplate Calibrator template 2 10 copies in each qPCR replicate Expected C value is 10 15 Recommendation Prepare for a slightly larger number of reactions to avoid run ning out of master mix during pipetting Add all components vortex gently spin down and dispense in replicates The primer stock concentration is 2 uM note the different concentration compared to other TATAA primer products This to achieve more accurate liquid handling for such a low number of replicates We advise add ing 2 ul of IPC per sample as pipetting of larger volumes is more accurate It is not necessary to include a non template control NTC for IPC 3 Perform qPCR with the protocol recommended for your reagents and as optimized for
14. ves of all the assays in all the samples compared in the experiment Figure 3 To achieve that all assays should be validated and any inhibited reaction should be excluded MIQE guidelines Bustin 2009 Given these requirements any baseline subtraction and threshold setting method can be used with the IPC If many different assays are used amplification curves are rarely all parallel Figure 6 The thresholds should be set at a level where the assay and the IPC response curves are parallel Figure 5 6 TATAA Interplate Calibrator SYBR Figure 5 Blue amplification curves are Figure 6 Blue amplification curves are TATAA Interplate Calibrator The curves TATAA Interplate Calibrator The thresh are parallel in complete range olds should be set at a level where the assay and the IPC response curves are parallel Different threshold settings 2nd derivative threshold common threshold manual or automatic best fit SD of noise TATAA Interplate Calibrator can be used if all the assays are well optimized and show similar amplification curves at least up to threshold Assay dependent threshold If different thresholds are set for different assays eg because of very different probe fluorescence a single TATAA Interplate Calibrator can still be used for all assays measured in the same instrument channel For every threshold setting an IPC C value is read and used for correction Inter in
15. x 400 nM primer 60 C 57 65 Biorad SsoFast EvaGreen Supermix 300 nM primer 60 C 55 61 Finnzymes DyNAmo ColorFlash SYBR Green qPCR Kit 400 nM primer 60 C 59 65 Finnzymes DyNAmo Flash SYBR Green qPCR Kit 400 nM primer 60 C 59 65 Invitrogen Express SYBR Greener 200 nM primer 60 C 57 65 KAPA SYBR FAST qPCR Kit 200 nM primer 60 C 57 63 Qiagen QuantiTect SYBR Green PCR Kit 300 nM primer 60 C 57 61 Quanta PerfeCTa SYBR Green Fastmix 300 nM primer Quanta PerfeCTa SYBR Green SuperMix 300 nM primer Roche FastStart Universal SYBR Green Master 300 nM primer 60 C 57 65 TAKARA SYBR Premix Ex Taq II Perfect Real time TAKARA SYBR Premix Ex Taq II Tli RNaseH Plus 400 nM primer 400 nM primer 60 C 59 65 60 C 59 65 60 C 55 62 TATAA SYBR GrandMaster Mix 300 nM primer 60 C 56 62 Thermo Scientific ABSOLUTE QPCR SYBR 400 nM primer 60 C 55 62 60 C 57 63 Concentration of each primer per qPCR Table 1 Recommended primer concentrations and annealing tempera tures in selected commercial master mixes Acceptable ranges of anneal ing temperatures to synchronize TATAA Interplate calibrator assay with other experimental assays are shown within parenthesis TATAA IPC as say perf
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