BIO RAD QX200 Instruction Manual Download Page 19

10 | QX200 Droplet Reader and QuantaSoft Software Instruction Manual 

QX200 Droplet Reader and QuantaSoft Software Instruction Manual | 11

Chapter 3 Using QuantaSoft Software

Chapter 3 Using QuantaSoft Software

3.1.1 Using the Well Editor

Use the well editor to define the settings (samples, experiment type, and detection type) for the plate. Sample 
and experiment types are color-coded and can be customized for easy reference in the plate map.

1. To open the well editor, double-click on the well(s) you wish to edit. Selected wells are highlighted in gray, 

and the well editor appears across the top of the interface.

To select multiple wells, hold 

Ctrl

 and select the wells

To select wells in a continuous series (horizontal or vertical), hold 

Shift

 and select the first and last wells

To select all wells in the plate, double-click in the top left corner of the plate

To select a row or column, double-click the letter or number for that row or column

2.  In the Sample panel, enter the sample 

Name

 and select the 

Experiment

 from the dropdown menu. 

All saved experiments appear in the dropdown menu, along with the option to

 add experiment... 

The sample name is case sensitive; only wells with identical sample names can be treated as merged 
wells during data analysis

To create or edit an experiment, use the experiment editor (see Section 3.1.2)

3.  Select the 

Supermix

 from the dropdown menu (required; selection cannot be changed after data collection).

Fig. 9. Assay type options.

Unused 

— channel unused

Unknown

 —

 

unknown experimental sample

Reference 

—  reference gene or target (required for CNV, RED, or  

ratio calculations)

Positive 

— positive control

Negative 

— negative control

Blank 

— no sample; use for wells that will not be analyzed

NTC 

— no-template control

Fig. 8. Well editor. 

Settings for absolute quantification of two unknowns in a single sample are shown.

Reset 

— restore default settings

Apply

 —

  

apply settings without exiting 
well editor

Cancel 

— close without saving changes

OK 

— save changes and close well editor

Summary of Contents for QX200

Page 1: ...QX200 Droplet Reader and QuantaSoft Software Instruction Manual Catalog 1864001 1864003...

Page 2: ......

Page 3: ...ive owner EvaGreen is a trademark of Biotium Inc Bio Rad Laboratories Inc is licensed by Biotium Inc to sell reagents containing EvaGreen dye for use in real time PCR for research purposes only The QX...

Page 4: ...ruction manual may cause harmful interference to radio communications Operation of this equipment in a residential area is likely to cause harmful interference in which case the user will be required...

Page 5: ...in the Code of Federal Regulations CFR at 29 CFR 1910 132 General requirements 29 CFR 1910 138 Hand protection 29 CFR 1926 95 Criteria for standard personal protective equipment Any gloves with impai...

Page 6: ...iv QX200 Droplet Reader and QuantaSoft Software Instruction Manual...

Page 7: ...2 Using the Experiment Editor 12 3 1 3 Using the Advanced Options 13 3 2 Run 13 3 3 Analyze 14 3 3 1 Viewing Channel Data 16 3 3 2 Viewing Scatter Plots 18 3 3 3 Viewing Concentration Data 19 3 3 4 V...

Page 8: ...vi QX200 Droplet Reader and QuantaSoft Software Instruction Manual vi QX200 Droplet Reader and QuantaSoft Software Instruction Manual...

Page 9: ...following PCR for downstream applications such as sequencing or cloning The ddPCR System lets you Detect rare DNA target copies with unmatched sensitivity Determine copy number variation with unrivale...

Page 10: ...be different Component Description Catalog QX200 Droplet Generator QX200 Droplet Generator Instrument used for droplet generation 1864002 DG8 Droplet Generator Microfluidic cartridge used to mix sampl...

Page 11: ...rol for Probes 1863052 Reagents for EvaGreen detection PCR supermix QX200 ddPCR EvaGreen Supermix 1864033 1864034 1864035 1864036 Droplet generation oil Droplet Generation Oil for EvaGreen 1864005 186...

Page 12: ...ad after thermal cycling and four will not be read Analyze results the droplet reader connects to a laptop computer running QuantaSoft Software The software provides a complete set of tools for settin...

Page 13: ...he lights are flashing amber the run cannot be started replace the oil or waste bottle see Section 4 2 2 Table 2 1 Status indicator lights on the QX200 Droplet Reader Solid green Power on Bottle level...

Page 14: ...lid again to close the cover Confirm the first three indicator lights are green Table 2 1 Fig 2 Placing the 96 well plate into the plate holder Base of plate holder 96 well PCR plate Top of plate hol...

Page 15: ...te holder lid is flat on top of the plate and the clamps are locked down Failure to do so could cause the sampling needle to run into the lid damaging the instrument Fig 4 Correct and incorrect placem...

Page 16: ...8 QX200 Droplet Reader and QuantaSoft Software Instruction Manual 8 QX200 Droplet Reader and QuantaSoft Software Instruction Manual...

Page 17: ...see Section 3 1 Run start the run and control the instrument if needed see Section 3 2 Analyze compute nucleic acid concentration see Section 3 3 QuantaSoft Software uses the following file types Tem...

Page 18: ...te click Template New To overwrite the setup information for a plate that is open experiment type and name sample name etc click Template Load In the Load Template window click Overwrite Fig 5 QuantaS...

Page 19: ...In the Sample panel enter the sample Name and select the Experiment from the dropdown menu All saved experiments appear in the dropdown menu along with the option to add experiment The sample name is...

Page 20: ...n the experiment editor select Experiment add experiment in the well editor or select New or Edit double click on an experiment name in the Experiments window under Setup Three types of experiments ar...

Page 21: ...ross the top navigation area Once the run is complete all data are reanalyzed for the final data file 3 2 Run 1 Click Run in the left navigation bar to start the run 2 In the Run Options window select...

Page 22: ...election of wells for targeted analysis Processed data graphical display allows visualization of graphical data from selected wells Fig 13 Interface during an active run Data for both detector channel...

Page 23: ...ual analysis tools To get more details of an error hover over the check tab with the mouse arrow Multi data automatically analyzed as part of a multi well selection Manual droplets analyzed manually F...

Page 24: ...processed data plots show where droplet data from each well start and end and the assigned threshold appears as a horizontal pink line Use the multi well threshold tool to change the threshold in all...

Page 25: ...nt tool single well Reset automatic threshold settings Y axis log scale toggle Threshold settings Fig 18 Viewing channel data for multiple wells Processed data from both channels of multiple wells are...

Page 26: ...he whole plot the clustering tool is disabled when viewing the plot in heat map mode Use the ellipse rectangle or lasso threshold adjustment tool to classify a region of the plot Click the tool then c...

Page 27: ...oisson confidence limits Solid data points shown indicate merged data open data points not shown indicate data from single wells Toggle y axis log scale Display data from single wells merged data or b...

Page 28: ...reaction Chapter 3 Using QuantaSoft Software Toggle well name or label display Fig 21 Viewing copy number data Hover over data points to reveal well identity concentration and Poisson confidence limi...

Page 29: ...the desktop Open this mode from the Start menu otherwise files automatically open in the regular version of QuantaSoft Simulation mode allows you to perform functions from the top right menu that are...

Page 30: ...22 QX200 Droplet Reader and QuantaSoft Software Instruction Manual 22 QX200 Droplet Reader and QuantaSoft Software Instruction Manual...

Page 31: ...ree 2 indoor use Installation category II external power supply plugs into standard AC receptacle Ventilation requirements 5 12 cm left and right of machine and 10 25 cm behind should be unobstructed...

Page 32: ...ader fluids are based on fluorinated hydrocarbon chemistry and should be disposed of in accordance with institutional state and local regulations These nonflammable fluids are inert and have low envir...

Page 33: ...roducts which will serve as a substrate for microbial growth mold and fungus To avoid instrument damage always be sure to add 50 ml of 10 bleach to the empty waste bottle to prevent microbial growth F...

Page 34: ...ice You should contact Technical Support All other error codes Since the computer directly controls the instrument s fluidics problems with computer performance can trigger instrument errors The first...

Page 35: ...for use in nucleic acid sample preparation with the QX200 Droplet Generator 1863024 ddPCR Supermix for Probes No dUTP 5 ml 5 x 1 ml 2x supermix for use in nucleic acid sample preparation with the QX2...

Page 36: ...leic acid sample preparation with the QX200 Droplet Generator 1864035 QX200 ddPCR EvaGreen Supermix 25 ml 5 x 5 ml for use in nucleic acid sample preparation with the QX200 Droplet Generator 1864036 Q...

Page 37: ...Pkg 1 000 rxns 12003805 ddPCR HDR Ref Assay Predesigned 100 rxns 12003806 ddPCR HDR Ref Assay Predesigned 500 rxns 12003793 ddPCR HDR Ref Pkg Predesigned 1 000 rxns 12002314 ddPCR NHEJ Gene Edit Assa...

Page 38: ...30 QX200 Droplet Reader and QuantaSoft Software Instruction Manual...

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Page 40: ...ungary 36 01 459 6190 India 91 124 4029300 Israel 972 03 963 6050 Italy 39 02 49486600 Japan 81 3 6361 7000 Korea 82 2 3473 4460 Mexico 52 555 488 7670 The Netherlands 310 318 540 666 New Zealand 64 9...

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