Human Parainfluenza Virus Type 2 Real Time RT-PCR Kit
Contents
1. Liferiver Revision No ZJO003 Issue Date Jul 1 2012 Human Parainfluenza Virus Type 2 Real Time RT PCR Kit C User Manual 20 C Z I For In Vitro Diagnostic Use Only RR 0157 01 rw N ZJ Bio Tech Co Ltd www liferiver com cn Tel 86 21 34680596 For use with LightC ycler1 0 2 0 Instrument trade liferiver com cn Fax 86 21 34680595 pec rer Obelis S A Boulevard G n ral Wahis 53 1030 Brussels BELGIUM Tel 32 2 732 59 54 2 floor No 15 Building No 188 Xinjunhuan road Fax 32 2 732 60 03 PuJiang Hi tech Park Shanghai China E Mail mail obelis net 1 Intended Use Human Parainfluenza Virus Type 2 real time RI PCR kit is used for the detection of Human Parainfluenza Virus Type 2 in nasal and pharyngeal secretions by using real time PCR systems 2 Principle of Real Time PCR The principle of the real time detection is based on the fluorogenic 5 nuclease assay During the PCR reaction the DNA polymerase cleaves the probe at the 5 end and separates the reporter dye from the quencher dye only when the probe hybridizes to the target DNA This cleavage results in the fluorescent signal generated by the cleaved reporter dye which is monitored real time by the PCR detection system The PCR cycle at which an increase in the fluorescence signal is detected initially Ct is proportional to the amount of the specific PCR product Monitoring the fluorescence intensities during Real Time allows the detection of2. e All reagents should be stored at 20 C Storage at 4 C is not recommended e All reagents can be used until the expiration date indicated on the kit label e Repeated thawing and freezing gt 3x should be avoided as this may reduce the sensitivity of the assay e Cool all reagents during the working steps e Super Mix should be stored in the dark 6 Additionally Required Materials and Devices e Biological cabinet e Real time PCR system e Desktop microcentrifuge for eppendorf type tubes RCF max 16 000 x g e Vortex mixer e RNA extraction kit e Real time PCR reaction tubes plates e Cryo container e Pipets 0 5 ul 1000 ul e Sterile filter tips for micro pipets e Sterile microtubes e Disposable gloves powderless e Biohazard waste container e Refrigerator and freezer e Tube racks 7 Warnings and Precaution Carefully read this instruction before starting the procedure e For in vitro diagnostic use only e This assay needs to be carried out by skilled personnel e Clinical samples should be regarded as potentially infectious materials and should be prepared in a laminar flow hood e This assay needs to be run according to Good Laboratory Practice e Do not use the kit after its expiration date e Avoid repeated thawing and freezing of the reagents this may reduce the sensitivity of the test e Once the reagents have been thawed vortex and centrifuge briefly the tubes before use e Prepare quickly the Reaction mix on ic
3. 38 40 Re test If it is still 38 40 report as 1 PCR Inhibition No diagnosis can be concluded For further questions or problems please contact our technical support at trade liferiver com cn i Positive and the software displays the quantitative value
4. e or in the cooling block e Set up two separate working areas 1 Isolation of the RNA DNA and 2 Amplification detection of amplification products e Pipets vials and other working materials should not circulate among working units e Use always sterile pipette tips with filters e Wear separate coats and gloves in each area e Do not pipette by mouth Do not eat drink smoke in laboratory e Avoid aerosols 8 Sample Collection Storage and transport e Collected samples in sterile tubes e Specimens can be extracted immediately or frozen at 20 C to 80 C e Transportation of clinical specimens must comply with local regulations for the transport of etiologic agents 9 Procedure 9 1 RNA Extraction Different brand RNA extraction kits are available You may use your own extraction systems or the commercial kit based on the yield For the RNA extraction please comply with the manufacturer s instructions The recommended Extraction kit is as follows Nucleic Acid Isolation Kit Cat Number RNA Isolation Kit ME 0010 ME 0012 ZJ Biotech 9 2 Internal Control It is necessary to add internal control IC in the reaction mix Internal Control IC allows the user to determine and control the possibility of PCR inhibition Add the internal control IC 1ul rxn and the result will be shown in the 560nm Channel 9 3 Quantitation The kit can be used for quantitative or qualitative real time RT PCR A positive control defined as 1x10 copi
5. es ml is supplied in the kit For performance of quantitative real time PCR Standard dilutions must prepare first as follows Molecular Grade Water is used for dilution Dilution is not needed for qualitative real time PCR detection Take positive control 1x10 copies ml as the starting high standard in the first tube Respectively pipette 36ul Molecular Grade Water into next three tubes Do three dilutions as the following figures Dilution of Standards Aul Aul 4ul Y VY V Y 1X107 1X10 1X10 1X 104 copiesim To generate a standard curve on the real time system all four dilution standards should be used and defined as standard with specification of the corresponding concentrations Attention A Mix thoroughly before next transfer B The positive control 1x10 copies ml contains high concentration of the target DNA Therefore be careful during the dilution in order to avoid contamination 9 4 RT PCR Protocol The Master Mix volume for each reaction should be pipetted as follows 134l 1 yl 1y Super Mix Enzyme Mix Internal Control Sul 15l Extraction RNA Master Mix Reaction Plate Tube i PCR Instrument XPCR system without 560nm channel may be treated with 1ul Molecular Grade Water instead of 1ul IC 1 The volumes of Super Mix and Enzyme Mix per reaction multiply with the number of samples which includes the number of controls standards and sample prepared Molecular Grade Water is used as the negative control For reas
6. ons of unprecise pipetting always add an extra virtual sample Mix completely then spin down briefly in a centrifuge 2 Pipet 15ul Master Mix with micropipets of sterile filter tips to each of the Real time PCR reaction plate tubes Separately add 5ul RNA sample positive and negative controls to different reaction plate tubes Immediately close the plate tubes to avoid contamination 3 Spin down briefly in order to collect the Master Mix in the bottom of the reaction tubes 4 Perform the following protocol in the instrument Fluorescence measured at 60 C 10 Threshold setting Choose Arithmetic as back ground and none as Noise Band method then adjust the Noise band just above the maximum level of molecular grade water and adjust the threshold just under the minimum of the positive control 11 Calibration for quantitative detection Input each concentration of standard controls at the end of run and a standard curve will be automatically formed 12 Quality control Negative control positive control internal control and QS curve must be performed correctly otherwise the sample results is invalid 530nm Molecular Grade Water Positive Contol qualiaiveasayy 35 QS quantitative detection 13 Data Analysis and Interpretation The following sample results are possible Crossing point value l Result Anal O Tam T sam OO Patam 5 1 25 35 Below the detection limit or negative 25 Selection of fluorescence channels
7. the accumulating product without having to re open the reaction tube after the amplification 3 Product Description Human parainfluenza viruses are second to respiratory syncytial virus RSV as a common cause of lower respiratory tract disease in young children Similar to RSV HPIVs can cause repeated infections throughout life usually manifested by an upper respiratory tract illness e g a cold and or sore throat HPIVs are negative sense single stranded RNA viruses that possess fusion and hemagglutinin neuraminidase glycoprotein spikes on their surface There are four serotypes types of HPIV 1 through 4 and two subtypes 4a and 4b Each of the four HPIVs has different clinical and epidemiologic features The most distinctive clinical feature of HPIV 1 and HPIV 2 is croup i e laryngotracheobronchitis HPIV 1 is the leading cause of croup in children whereas HPIV 2 is less frequently detected Both HPIV 1 and 2 can cause other upper and lower respiratory tract illnesses HPIV 2 causes annual or biennial fall outbreaks The Human Parainfluenza Virus Type 2 real time RT PCR kit contains a specific ready to use system for the detection of the Human Parainfluenza Virus Type 2 using RT PCR Reverse Transcription Polymerase Chain Reaction in the real time PCR system The master contains a Super Mix for the specific amplification of the Human Parainfluenza Virus Type 2 RNA The reaction is done in one step real time RT PCR The first step is a re
8. verse transcription RT during which the Human Parainfluenza Virus Type 2 RNA is transcribed into cDNA Afterwards a thermostable DNA polymerase is used to amplify the specific gene fragments by means of PCR polymerase chain reaction Fluorescence is emitted and measured by the real time systems optical unit during the PCR The detection of amplified Human Parainfluenza Virus Type 2 DNA fragment is performed in fluorimeter channel 530nm with the fluorescent quencher BHQ1 In addition the kit contains a system to identify possible PCR inhibition by measuring the 560nm fluorescence of the internal control IC An external positive control defined as 1x10 copies ml is supplied which allow the determination of the gene load For further information please refer to section 9 3 Quantitation 4 Kit Contents HPIV 2 Super Mix 1 vial 350u1 RT PCR Enzyme Mix 1 vial 28ul Molecular Grade Water 1 vial 400u1 Internal Control IC 1 vial 30u1 HPIV 1 Positive Control 1x10 copies ml 1 vial 30ul Analysis sensitivity 1X 10 copies ml LOQ 2X10 1X 10 copies ml Note Analysis sensitivity depends on the sample volume elution volume nucleic acid extraction methods and other factors If you use the RNA extraction kits recommended the analysis sensitivity is the same as it declares However when the sample volume is dozens or even hundreds of times greater than elution volume by some concentrating method it can be much higher 5 Storage
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