SybGREEN qPCR Primers and Standards
Contents
1. ion exchange columns linearized by a restriction enzyme and quantified by the Picogreen method The Picogreen method relies upon an ultra sensitive fluorescent nucleic acid stain and has a much higher accuracy than a UV spectrophotometer for determining DNA concentration The process for the preparation of a qPCR standard is illustrated in Figure 1 Figure 1 Preparation of qPCR Standard A B 230000 220000 210000 200000 hd 190000 180000 170000 160000 150000 140000 130000 120000 110000 100000 90000 80000 70000 60000 50000 40000 30000 20000 10000 A An EcoRI linearized qPCR template standard is run on a 1 agarose gel B Plot of a template DNA and PicoGreen standard from a PicoGreen assay The concentration of the template DNA is converted from ng per ul to copy number per ul using the following formula C 10 MW Na C template concentration ng ul MW template molecular weight in Daltons Na Avogadro s constant 6 022 x 107 Figure 2 Preparation of qPCR Standard dilution 10 ul 10 ul 10 ul 10ul 10 ul 10 ul E AANAND 1x 10 ul 90 ul 1 2 3 4 5 6 10 108 10 10 10 10 copy ul Experimental Procedures qPCR protocol Preparation of the qPCR template standard 1 The qPCR template standard is provided as a dried pellet Add 50 ul of d H20 to the tube and vortex briefly The resuspended template is 102. proportionally The recommended reaction volume for 384 is 10 ul SYBR Green method Prepare the cocktail as follows 64X solution 2 x Master mix 800 ul Primer mix 64 ul H20 416 ul 1 300 ul Taqman probe method Probe method 2 x Master mix 800 ul 20 x Taqman Probe 80 ul with the gene specific primers included H20 420 ul 1 300 ul Figure 3 Suggested Plate Layout 0000080000008 OOOO00O000000O 000000000000 000000000000 0000000000080 000000000000 OOOO0O0O0O000O00O 0000008000080 PCR standard O Unknown C Empty well qPCR setup N a Dew oo N Transfer 5 ul of each of the six qPCR Template Standard dilutions to Row A in duplicate Add 5 ul of each unknown sample to row C D E and F The amount of cDNA in each reaction is ideally around 1 to 10 ng diluted with the dilution buffer included Add 20 ul of PCR cocktail to each of well of row A C D E and F Seal the PCR plate with a real time PCR sealer Mount the plate to a real time PCR machine such as ABI 7900HT Set up the PCR run according to the machine s user manual Be sure to input the copy number when setting up the PCR standards using the standard curve method Start the PCR reaction Analyze the data according to the machine s user manual Calculation of the copy number of your gene of interest 1 If the cDNA templates in your samples are single stranded such as cDNA from RT reactions the actual copy number of your gen
3. 000 000 copy ul Thaw the 10 x dilution buffer tube from the kit at room temperature 2 Ifthe SYBR Green method is used reconstitute SyoGREEN primer by adding 200 ul d H20 to the primer tube and vortex it briefly The resuspended primers are 10 pmol ul each Omit this step if Taqman probe method is used 3 Prepare 1 0 mL of 1 x dilution buffer by adding 100 ul of the 10 X buffer to 900 ul H20 4 Label six 6 Eppendorf tubes from 1 to 6 Transfer 90 ul of 1x buffer to each pre labeled eppendorf tube 1 to 6 5 Transfer 10 ul of template standard from the stock tube to eppendorf tube 1 Fig 2 Mix the solution by briefly vortexing Transfer 10 ul solution from tube 1 to tube 2 then mix the solution by vortexing Perform remaining dilutions by repeating steps 5 and 6 Transfer 5 ul of diluted template solution from each tube to a 96 well PCR plate use 2 ul when a 384 well plate is used 0 NO Preparation of PCR mix The qPCR template standard can be used with either the Taqman probe based method or the SYBR Green method Step one calculate the total volume of the PCR mixture based on the number of the total samples The following recipes are for setting up a cocktail for 60 samples 6 template standard dilutions in duplicate and 48 unknown samples The qPCR reaction volume is 25 ul volume in 96 well format for both the SYBR Green method and the Taqman probe method When the 384 well format is adopted reduce all reagents
4. 7 Package Contents and Storage Conditions For SyoGREEN primer only e 1 Vial SyoGREEN qPCR primer mix 2 nmol lyophilized sufficient for 200 reactions Before use reconstitute the primer mix in 200 ul dH20 to make a final concentration of 10 uM e Application Guide For SybGREEN primer and qPCR standard kit e 1 Vial SyoGREEN qPCR primer mix 2 nmol lyophilized sufficient for 200 reactions e 1 Vial Gene Specific qPCR template standard 50 X 10 Copies double stranded DNA lyophilized Add 50 ul of d H20 to the tube and vortex briefly The resuspended template is 10 000 000 copy ul e 1 Vial containing 1 mL 10 x PCR template standard dilution buffer e Application guide The above components are shipped at room temperature but should be kept at 20 C for long term storage If properly stored they have a 12 month shelf life The polymerase chain reaction PCR is protected by patents held by Hoffmann La Roche Purchase of any of OriGene s PCR related products does not convey a license to use the PCR process covered by these patents Purchasers of these products must obtain a license before performing PCR see page 6 on how to calculate the copy number of an unknown sample NOTE FOR RESEARCH PURPOSES ONLY NOT FOR DIAGNOSTIC OR THERAPEUTIC USAGE Introduction Real time PCR is one of the most important approaches in detecting the transcript level of a gene in a particular cell or tissue sample Two types of real ti
5. SybGREEN qPCR Primers and Standards Tools for RT PCR Application Guide Table of Contents Package Contents and Storage Conditions ccc eeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeee 1 Introduction asd cectanpaceeadcadouadsnnsonsdenavonaisdetenatetsborstad decals atangbstseosalsd steeadinsuaesdsaglndebanbons 3 SYOGREEN GPCR Primer Pale wcccccicsscesssavsiersserisantaasanadieesrereaeeenieaws 3 Gene Specific qPCR Template Standards cccccccccecceeeeeeeeeeeeeeeeeeeensseeeeeeess 3 Figure 1 Pr paration of qPCR Standard siciicsssiscceseseranccadisaxetanwiersiatetenandeicianiotnciond 4 Figure 2 Preparation of qPCR Standard dilution eeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeees 4 Experimental Procedures 2 cccccccccccesseeeeeeeeeeceeeeeeesseeeeeeeeeeeeeeauseeeeeeeseeeeeeaaeeees 5 qPCR protocol Preparation of the qPCR template standard ccccceeeeeeeeeeees 5 Preparation of PCR MiX nnnnannnnnnennnnnnnrnnnnnrrrnnnnnrrrnnnrrrrnnnrrrennnrrrnnnnnrnnnnnnrennnnnrennnn 5 Figure 3 Suggested Plate Layout 22 2220 cccccccccenccenecenetenssenetenesenetentsenedestinsetonddonetonene 6 AEC go 1 9 Regeeenete ser cneets E nent Meet ior Ment meet Meer Meo Merten eeremert ra Ter 6 Figure 4 Sample data SYBR Green Real Time PCR on ABI9700HT 7 Trouble s hooting Guide asic ccctisnc cece teenth cnc see een EEEREN 7 Frequently Asked OUCStONS c50 scce cee ee eee eee eee
6. e of interest is two times the number you got by comparing to the qPCR standards For example if the copy number of your gene is 5 copy ul from the standard curve of a qPCR program the actual number is 10 copy ul The reason is that the first cycle for a single stranded sample is to make the complementary strand therefore there is one cycle delay in the PCR reaction compared to the double stranded cDNA template standard s reaction If the templates in your samples are double stranded the copy number of your gene of interest is the same as that calculated according to the qPCR standards Figure 4 Sample data SYBR Green Real Time PCR on ABI9700HT qPCR Template Standard and primer pair for NM_004808 Human N myristoyltransferase 2 NMT2 Arete Nt a Detector free erry Real time PCR data were obtained by using serial dilutions of a PCR standard for NM_004808 as the template with specific primers The PCR was performed on the ABI 7900HT utilizing the SYBR method The plot of Act vs cycle number for qPCR Template Standard is shown on the left with copy numbers from 10 000 000 to 10 per ul and the concentration dilution plot is shown on the right An unknown sample breast cancer tissue cDNA is detected to contain approximately 37 copies ul of NMT2 based on the standard curve results Trouble shooting Guide No qPCR product detected 1 A qPCR component may have been omitted in the reaction Be sure to
7. emplate standard A A gene specific qPCR template standard is a tube of linear DNA made from a full length cDNA plasmid The copy number of a template standard solution is determined by the PicoGreen method and calculation based on MW Q Can a template standard be used in a probe based qPCR A Yes as long as a corresponding probe is used Q In your protocol it is recommended to make six serial dilutions with one log of difference can make more dilutions and with different dilution scheme A Yes as long as it is diluted in the qPCR detection range and each dilution is mixed thoroughly Q Can I use my own buffer to dilute the template standard instead of the buffer in the kit A Yes as long as the buffer has no negative effects on qPCR Q Does OriGene offer custom made template standards A Yes Please contact our Tech Support at techsupport origene com Q What is the OriGene guarantee on qPCR primers and template standards A OriGene qPCR primers and templates are warranted for SYBR Green qPCR experiments If your experimental results are not satisfactory our scientists will work with you to pinpoint the problem and if it is determined that our products are at fault OriGene will refund your money in the form of a credit
8. me PCR protocol are currently used One is probe based and the other is SYBR Green based The two protocols utilize fluorescent probes or dyes that are proportional to the amount of the PCR products generated at the end of each cycle Differences between the two methods involve the types of fluorescent signals and the ways in which the signals are generated In the TaqMan protocol a pair of gene specific amplification primers and a sequence specific fluorogenic probe is present in the PCR mixture During amplification the probes anneal proportionally to the single strand amplicons and are subsequently removed base by base by the 5 exo nuclease activity of Taq polymerase Consequently the released fluorescence moiety generates fluorescent signals that are proportional to the amount of PCR product generated This method is very sensitive and reliable The SYBR Green protocol on the other hand does not require a sequence specific fluorescent probe SYBR Green binds to double stranded DNA to generate detectable fluorescence and the amount of signal is proportional to the amount of double stranded DNA present Since SYBR Green binds indiscriminately to double stranded DNAs it will generate false signals if non specific DNA contamination exists Nevertheless it is frequently used in many laboratories due to its simple protocol and low cost SybGREEN qPCR Primer Pairs The key components of a successful qPCR are the primers used to amplify
9. the template Only well designed primers can give trustworthy expression data using qPCR Poor primer design usually results in non specific PCR products and or primer dimers These undesired DNA byproducts will interact equally well with SYBR Green reagents and therefore generate a false positive signal To design primers with a high specificity and a low incidence of primer dimer formation OriGene conducted a large scale study of qPCR involving thousands of primers Based on the vast PCR data acquired through this study OriGene scientists were able to develop a superb primer design algorithm With this algorithm OriGene is able to provide our customers with genome wide pre designed ready to use qPCR primers Besides high specificity and high efficiency each primer pair is also selected to span exon junctions whenever possible thus avoiding the amplification of genomic DNA Each primer pair is supplied as 2 nmol lyophilized powder Before use reconstitute the primer mix in 200 ul dH20 to make a final concentration of 10 uM Gene Specific qPCR Template Standards A known qPCR template standard serves two main purposes It functions as a positive control and as a reference for measuring the exact copy number of a transcript in an unknown sample OriGene has a large collection of full length human and mouse cDNA constructs which are ideal PCR templates To increase the accuracy of DNA quantification a full length cDNA is purified using high purity
10. use a checklist when assembling the reaction mix 2 Make sure the master mix is working by using a positive template control 3 The sample used may have very limited qPCR template Add more sample or prepare efficient templates by using a better reverse transcriptase The standard curve generated is not linear The dilution of the Template Standard may have been done incorrectly Use an accurate pipette and mix each dilution sample thoroughly A Ct value is out of the range of the standard curve If the Ct reading for an unknown sample is too small high abundance of a template dilute the sample further If the Ct is too high low abundance of a template then dilute the template standard further or use more unknown sample Frequently Asked Questions Q What are SyoGREEN qPCR Primer Pairs A SyoGREEN qPCR Primer Pairs are pre designed qPCR tested and ready to use primer sets for SYBR Green based qPCR experiments Q Can SybGREEN qPCR Primer Pairs be used in probe based qPCR 7 A No This kit has not been designed to accommodate any commercial probe based qPCR Q What is the Tm of the primer and what is a typical size of the amplicon A The Tm of a SyoGREEN qPCR Primer is around 60 and the amplicon is around 95 to 140 bp Q Does a SybGREEN qPCR Primer Pair amplify an exon junction in a cDNA target A Whenever possible an amplicon by a SyoOGREEN qPCR Primer Pair covers exon junction or junctions Q What is a qPCR t
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