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Instruction for Use HISTO TYPE Rainbow QS6 

Version: 02/2021 

Page 7 of 16 

 

Please note:

 When pipetting into the PCR wells it is important not to allow the pipette tip to contact 

the dried mix (dyed blue) in the bottom of the well. It is advisable to pipette to the side of the well to 
allow the 10 µl to mix by gravity with the dried mix (see Figure 1). 
 

 

Figure 1 

 
 

 

 

Figure 2: 

HISTO TYPE Rainbow QS6 plate. In wells A1 to G12 are the dried specific mixes (blue coloured). In well H12 
there is the dried NTC (also blue). 

 
Seal the PCR plate with the supplied qPCR seal and briefly spin the liquid down. Make sure that the 
plate  is 

completely  sealed

,  particularly  at  the  edge  of  the  plate.  Make  sure  that  the  liquid  has 

contacted  the  dried  mix  and  there  are 

no  bubbles

  or  air  gaps  in  the  reaction  wells.  If  bubbles 

appear,  gently  tap  the  tubes  on  the  laboratory  bench  to  remove them, or  preferably  careful spin it 
down (10 sec). 
 
Place  the  sealed  PCR  plate  in  the  QS6  instrument.  Please  use  the  correct  plate  holder  and 
orientation as per the notes below. 

 
Note:

  Please make sure that you place the reaction plate into the cycler in the correct orientation 

as shown in Figure 2 above where the NTC well is in the bottom right corner, position H12. 

Note:

  For  the  HISTO  TYPE  Rainbow  plates  a  special  plate  holder  for  the 

QuantStudio™  6  Flex 

System  is  required,  which  is  included  in  the  first  starter  package  (REF  726321).  For  more 
information please contact BAG Diagnostics. 

 

 
 
 
 

Содержание HISTO TYPE Rainbow QS6

Страница 1: ...ample information into PlexTyper Software 5 6 4 Amplification 5 6 5 Export of results from QuantStudio 6 Flex System 9 6 6 Evaluation and interpretation of the results 10 6 7 Import of the results fil...

Страница 2: ...s amplified in a real time PCR with sequence specific primers SSP The primers were specially developed for the selective amplification of segments of specific HLA alleles or allele groups The amplicon...

Страница 3: ...2 Real time PCR Cycler validated cycler see 4 3 Plate holder QS6 REF 726321 Variable pipettes 0 5 1000 l and pipette tips Application spatula for qPCR Seal Molecular grade DNAse free water Suitable pl...

Страница 4: ...amplification detection use two separate rooms if possible Use devices and other materials only at the respective workplaces and do not exchange them 6 2 DNA Isolation The specimen material for the i...

Страница 5: ...entity This Run ID should be used when setting up the file identity in the PCR machine If the PCR excel export file is not pre labelled with the RUN ID the file can be manually prefixed with the corre...

Страница 6: ...te the test DNA with other concentrations For DNA of different stock concentrations use the dilution table below to adjust the DNA to working concentration Add 8 l Molecular grade water and 2 l Plex M...

Страница 7: ...ely sealed particularly at the edge of the plate Make sure that the liquid has contacted the dried mix and there are no bubbles or air gaps in the reaction wells If bubbles appear gently tap the tubes...

Страница 8: ...Flex System Block type Fast 96 Well 0 1mL Experiment type Comparative Ct Ct Reagent type TaqMan Reagents Run properties Standard Define Targets Please note Custom dye instrument calibration must be p...

Страница 9: ...rt the raw data in excel format with the following steps 1 Select the eds file double click on a eds file If the QuantStudio RealTime PCR software is installed the software will automatically open the...

Страница 10: ...s required for the evaluation are available from the BAG Diagnostics download server www service bag diagnostics com Please make a note of the lot number of the kit The interpretation kit files are pr...

Страница 11: ...s possible contamination by the PlexTyper software and a warning message is generated Amplification signals above Cq 36 in the NTC are regarded as PCR artefacts and are disregarded If PCR contaminatio...

Страница 12: ...No results at an HLA locus 7 WARNINGS AND DISPOSAL INSTRUCTIONS HISTO TYPE Rainbow QS6 is designed for in vitro diagnostic use The kit should only be used by specially trained qualified personnel All...

Страница 13: ...t is checked for each lot with control specimens with known HLA alleles The kit determines the HLA Loci A B C DRB1 DRB3 DRB4 DRB5 DQA1 DQB1 DPA1 and DPB1 8 1 SPECIFIC PERFORMANCE CHARACTERISTICS 8 1 1...

Страница 14: ...n to avoid contamination of kit reagents and other laboratory materials with amplicons or DNA The performance of a negative control without DNA in well H12 is strongly recommended No fluorescence sign...

Страница 15: ...ll of the tube Careful pipetting Spin down PCR plate User error Ensure all wells receive the required volume of reagents Evaporation of the reagents due to incorrect closing of the PCR tubes Make sure...

Страница 16: ...ue number RTU Ready to use 14 LITERATURE 1 Mack S J et al 2013 Tissue Antigens 81 194 203 2 Beutler E et al 1990 BioTechniques 9 166 15 REVIEW HISTORY Version 01 2021 Issue 2021 04 Initial version Ver...

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