qTOWER 2.0 /qTOWER 2.2: Real-Time PCR Thermal Cycler
qTOWER 2.0 /qTOWER 2.2: Real-Time PCR Thermal Cycler
Operating manual
Service: Analytik Jena AG
Customer Services
Konrad-Zuse-Str. 1
07745 Jena
Germany
This publication describes the state of this product at the time of publishing. It need not necessarily
agree with future versions of the product.
Modifications reserved!
© Copyright 2012 Analytik Jena AG
Contents
Table of Contents
1 Basics.................................................................................................... 3
1.1 Intended Use .................................................................................................. 3
1.2 Notes on the manual ...................................................................................... 4
1.3 Warranty and liability ...................................................................................... 4
2 Safety instructions ............................................................................... 5
2.1 Symbols and signal words used ..................................................................... 5
2.2 Safety markings at the qTOWER 2.0/2.2 ....................................................... 5
2.3 Technical condition ......................................................................................... 6
2.4 Requirements for the operating personnel ..................................................... 6
2.5 Safety instructions, transport and installation................................................. 7
2.6 Safety instructions - operation ........................................................................ 7
2.6.1 General ........................................................................................................... 7
2.6.2 Safety instructions - Protection against explosion and fire ............................ 8
2.6.3 Safety instructions - electrical equipment....................................................... 8
2.6.4 Handling of samples, auxiliary and operating materials ................................. 8
2.6.5 Safety instructions - service and repair .......................................................... 9
2.7 Behavior during emergencies ........................................................................ 9
2.8 Standards and directives .............................................................................. 10
3 Technical data .................................................................................... 11
4 Device description and principle of operation................................. 13
5 Commissioning .................................................................................. 15
5.1 Site requirements ......................................................................................... 15
5.2 Connections and controls at the qTOWER 2.0/2.2 ...................................... 16
5.3 Installation and commissioning .................................................................... 18
5.4 Switching the qTOWER 2.0/2.2 on and off .................................................. 19
6 Inserting samples / Starting the PCR run ......................................... 21
7 Maintenance and care ........................................................................ 22
7.1 Cleaning the housing.................................................................................... 22
7.2 Cleaning the sample block ........................................................................... 22
7.3 Cleaning the lens array ................................................................................ 23
7.4 Installing color modules ................................................................................ 23
7.5 Replacing the fuses ...................................................................................... 27
8 Transport and storage ....................................................................... 28
8.1 Transport ...................................................................................................... 28
8.2 Returns ......................................................................................................... 28
8.3 Moving the qTOWER 2.0/2.2 within the laboratory ...................................... 29
8.4 Storage ......................................................................................................... 29
9 Decontamination certificate .............................................................. 30
10 Disposal .............................................................................................. 32
Index of Figures
Fig. 1 Structure of the qTOWER 2.0/2.2 ........................................................................... 13
Fig. 2 Schematic structure of the Epi fluorescence photometer in the qTOWER 2.0/2.2 14
Fig. 3 qTOWER 2.0/2.2 front view .................................................................................... 16
Fig. 4 qTOWER 2.0/2.2 opened ....................................................................................... 16
Fig. 5 qTOWER 2.0/2.2 backplate .................................................................................... 17
Fig. 6 Voltage selection switch at the bottom of the qTOWERs 2.0/2.2 ........................... 17
Fig. 7 Connection and power supply cables for the qTOWER 2.0/2.2 ............................. 18
Fig. 8 Schematic representation of the position of additional vessels in case of low
sample numbers ..................................................................................................... 21
Fig. 9 Position A1 on the sample block ............................................................................ 21
Fig. 10 Fuse holder at the qTOWER 2.0/2.2 ...................................................................... 27
1 Basics
1.1 Intended Use
qTOWER 2.0/2.2 is a thermal cycler for amplifying DNA by way of the polymerase chain
reaction (PCR) licensed for real-time PCR experiments. The license is limited to applications
outside of vitro diagnostics (research use only).
The integrated detector enables the measurement of the sample fluorescence in up to six
spectral channels during the PCR, with the filters used in the color or FRET modules being
exactly matched to the properties of the most frequently used fluorescence dyes, thereby
permitting a sensitive and selective detection of fluorescent PCR products.
Analytik Jena offers a number of color or FRET modules of which up to six can be installed
simultaneously in the device. Replacement and retrofit of color or FRET modules can be
easily accomplished.
qTOWER 2.0/2.2 is an open platform for real-time PCR and supports both intercalating dyes
as well as individual samples and kits of various manufacturers. qTOWER 2.0/2.2 can be
used in different applications, such as expression analyses, genotyping and the detection of
pathogens.
qTOWER 2.0/2.2 is fully controlled from the PC using the program qPCRsoft. qPCRsoft pro-
vides the following functions
Device control and monitoring
User Management
Context-sensitive help functions
Design of real-time PCR experiments and their evaluation
Storage of methods (templates) and measuring results (projects)
Planning and evaluation of
− Absolute quantifications
− Relative quantifications
− ΔΔCt analyses
− DNA melting curves
− Genotyping
Results printout
Results export to MS EXCEL or as CSV file
Results export to extended programs for the analysis of real-time PCR data (e.g.
qBASE, REST etc.) in preparation
Conventions
Instructions for action which occur in chronological order are numbered and combined into
action units and furnished with the corresponding results.
Lists which are not in chronological order are shown as itemized lists, sub-listings as bullet
points.
Safety notes are indicated by pictographs and signal words. The type and source of the
danger are stated together with notes on preventing the danger. The meaning of the picto-
graphs and signal words used is explained in section "Symbols and signal words used" p. 5.
The elements of the control and analysis program are indicated as follows:
Menu command, buttons, options etc. are indicated by small caps.
Menu commands of a command sequence are separated by slashes ( / ), e.g. FILE /
NEW.
Buttons are marked with square brackets, e.g. [ADD].
2 Safety instructions
2.1 Symbols and signal words used
The user manual uses the following symbols and signal words to indicate hazards or instruc-
tions. The safety instructions are always placed before an action.
WARNING
Indicates a potentially hazardous situation.
If it is not prevented death or most serious injuries (incapacitation) can result.
CAUTION
Indicates a potentially hazardous situation.
If it is not prevented light or minor injuries and material damage can result.
IMPORTANT
Indicates application hints and other especially useful information without any resulting haz-
ardous or damaging situations.
Warning against hot surface General warning sign Before opening the device
always disconnect the plug!
Auxiliary and operating materials as well as their containers may not be disposed in
domestic waste or enter the sewage system or the soil. The applicable regulations
for disposal of these materials must be meticulously observed.
Ensure good room ventilation in working rooms.
If only a few samples are treated, an (empty) vessel of the same height must addi-
tionally be placed at each corner position of the block. If the number of samples in
the block is too low, there is a risk of the vessels being damaged.
Device safety
The qTOWER2.0/2.2 complies with the safety standards
DIN EN 61010-1:2002
EMC compatibility
The qTOWER 2.0/2.2 has been tested for radio interference suppression and interference
resistance and meets the requirements of
DIN EN 61326-1 (2006-10)
DIN EN 61326-2-6 (2006-10)
Environmental compatibility
The qTOWER 2.0/2.2 has been tested for environmental compatibility and meets the re-
quirements of
DIN ISO 9022-2:2003-01
DIN ISO 9022-3:2000-09
DIN EN 60068-2-64:2009-04
DIN EN 60068-2-29:1995-03
DIN EN 60068-2-31:2009-04
EC directives
The qTOWER 2.0/2.2 is built and tested according to standards that fulfill the requirements
stipulated by the EC directives 2006/95/EC and 2004/108/EC. Each device leaves the manu-
facturer in a pristine and technically safe state. To maintain this condition and to ensure safe
operation, the operator must strictly observe the safety and operating instructions contained
in this manual. For accessories which have also been supplied, and system components
from other manufacturers, their operating instructions should be referred to.
Information regarding safety corresponds to the currently valid regulations of the European
Union. In other countries the applicable laws and country specific regulations have to be
complied with.
Besides the safety instructions in this user manual and the local safety regulations that apply
to the operation of the qTOWER 2.0/2.2 the general applicable regulations regarding acci-
dent prevention, occupational health and safety and environmental protection have to be
observed and complied with.
References to potential dangers do not replace the work protection regulations which must
be observed.
3 Technical data
Block format 96 wells
Sample volume 10 – 60µl
Lid temperature 30 – 110°C
Temperature gradient for 40°C
qTOWER 2.2
Max. heating rate* up to 5.5 °C/s
Max. cooling rate* up to 4.0 °C/s
Heating rate adjustment min. 0.1°C/s
Temperature uniformity ± 0.15°C at 55°C
(15 sec. after starting the ± 0.25°C at 72°C
clock) ± 0.50°C at 95°C
Temperature range 3 °C – 99 °C
Control accuracy ± 0.1 °C
Temperature increments min. 0.1°C/cycle
Time increments min. 1 s/cycle
Heated lid Manual opening mechanism, automatic contact pressure
Heated lid contact pressure 10 kg, automated
Dimensions (H x W x D) 59 cm x 27.5 cm x 33 cm
70 cm x 27.5 cm x 53 cm when opened
Mass 24 Kg
Energy supply
Operating voltage 100V, 110V, 230V
Line frequency 50 – 60 Hz
Power consumption (max.) Base unit max. 600 W
Device fuse 2 x TT 4.0 A H 250 V
1 x T 630 mA L 250 V
Operating conditions 15°C to 35°C, max. 70% rel. humidity,
max. 2000 m NN
Supported plastic products 96 well micro titer plates with optical film
8-place strips 0.2 ml with optical lids
0.2 ml individual vessels with optical lids
Sensitivity 1 nmol/l FAM at 30 µl sample volume in a 96 well PCR
plate
Test time 96 well plate (single measurement, 6 colors) approx. 6 s
Measuring range +/- 130,000 (+/-17 bit)
Dynamic range 9 log stages
Light source Three longlife high intensity LEDs (blue, white, red)
Detector High-sensitivity Channel Photo Multiplier (CPM)
Optimum signal/noise characteristics through efficient
noise suppression (decreased SNR (signal/noise ratio)
technology)
Color filter modules 6 color modules for all frequently used real-time PCR dyes
Color module 1 (470 nm/520 nm)
Color module 2 (515 nm/545 nm)
Color module 3 (535 nm/580 nm)
Color module 4 (565 nm/605 nm)
Color module 5 (630 nm/670 nm)
Color module 6 (660 nm/705 nm)
4 FRET filter combinations:
FRET module 1 (470 nm/580 nm)
FRET module 2 (470 nm/670 nm)
FRET module 3 (470 nm/705 nm)
FRET module 4 (515 nm/670 nm)
Software and PC
qPCRsoft Control and analysis program
Analysis methods Absolute quantification, relative quantification, ΔΔCt
method
Allelic discrimination, efficiency calculation
Export functions Excel, (REST, qBASE in preparation)
Data connection USB
PC software requirements Minimum Pentium IV, > 1 GHz
Operating system Windows XP (SP2) / VISTA / 7
Fluorescence spectrometer
An 8 channel Epi fluorescence photometer with fiber multiplexer and mechanical scanning
device is used as detector.
Light for exciting the dyes is emitted by three longlife LEDs in blue, white and red. The light
is passed through high performance optic fibers to collimator lenses, bundled and then trans-
ferred to the excitation filter of the color modules fitted to a rotating filter wheel. The light is
deflected via a beam divider and passed through additional optic fibers to a lens array in a
shuttle system scanning the sample block in columns. The light excites the fluorescence
dyes in the reaction mix. The fluorescence dyes then emit a light of higher wavelength that is
bundled through the lenses in the shuttle system and passed via the optic fibers back to the
color modules. In the color modules the light passes the beam divider followed by two emis-
sion filters and is then transferred for detection to the Channel Photomultiplier (CPM).
The filter wheel of the photometer can be populated freely with a choice of color filter mod-
ules. In addition, the system can be retrofitted with filters at any time, extending the applica-
tion spectrum of the device. A total of 10 color filter modules are available, including filter
modules having been optimized specifically for FRET applications, covering the absorption
spectra of all commonly used fluorescence dyes from the blue through to the red excitation
range.
Fig. 2 Schematic structure of the Epi fluorescence photometer in the qTOWER 2.0/2.2
5 Commissioning
5.1 Site requirements
Installation conditions
The following requirements are placed on the climatic conditions in the operating room of the
qTOWER 2.0/2.2:
Temperature range: +15 °C to +35 °C
max. humidity: 90 % at 30 °C
Air pressure: 0.7 bar to 1.06 bar
The laboratory atmosphere should be free of draft, corrosive vapors and vibration.
The site for the qTOWER 2.0/2.2 must meet the following requirements:
Do not locate the device directly near a door or window.
Place the device on a heat-resistant and acid-resistant surface.
Do not locate the device near sources of electromagnetic interference.
Avoid direct sunlight and radiation from heaters onto the analyzer; if necessary en-
sure air conditioning.
Never cover the air vents of the backplate of the device with other equipment or in-
stallations!
Keep a safety distance of at least 10 cm to other equipment or walls!
Space requirement
IMPORTANT
When opening the qTOWERs 2.0/2.2 the upper device hood tilts back. Allow adequate
space for this.
Energy supply
WARNING! ELECTRIC SHOCK!
The qTOWER 2.0/2.2 must only be connected to a properly grounded mains outlet in accord-
ance with the voltage specifications on the type plate!
1 heated lid
2 sample block
3 twistlock
The qTOWER is opened by folding back the upper part and the cover for the sample block
and fluorescence photometer it contains. To this end the handle is pressed in until the lock
disengages with a click and the upper part gently snaps open. The upper part can then be
folded back from the handle.
In addition to the mains switch on the equipment backplate the qTOWER 2.0/2.2 features a
touch-sensitive sensor (touch sensor) (3 in Fig. 3) on the equipment front for switching the
device into sleep mode and switching it back on again. During sleep mode the communica-
tion with the PC and the software is interrupted. During a PCR process the touch sensor is
disabled. To trigger a switching operation touch the sensor for eat least 3 seconds. A green
illuminated touch sensor indicates the operational readiness of the qTOWER 2.0/2.2, a red
illuminated one indicates the sleep mode. The touch sensor can be switched off using the
bridging switch. To this end the bridging (8 in Fig. 5) must be moved to "1". The qTOWER
2.0/2.2 is then only switched off and on via the mains switch.
1 mains cable
2 connection cable for data transfer
3 cable for the power supply of the
fluorescence spectrometer and the
sample block lid
4 USB cable for PC connection
Fig. 7 Connection and power supply cables for the qTOWER 2.0/2.2
1. Remove the qTOWER 2.0/2.2, connection cable and operating manual with the in-
stallation CD from the transport packaging and wait until the device has reached
room temperature.
2. If the color modules have not yet been installed, assemble the color modules in ac-
cordance with section "Installing color modules p. 23".
6. Connect the USB cable to the "USB" port of the qTOWER 2.0/2.2 and the PC.
7. Connect the mains cable to the qTOWER 2.0/2.2 and plug the connector into the
mains outlet.
8. Switch on the PC and install the qPCRsoft software on your PC. Observe the notices
in the software manual.
Note:
The qTOWER 2.0/2.2 is only supported from qPCRsoft program version 1.1.80.
9. Switch on the qTOWER 2.0/2.2 at the mains switch.
During first startup the qTOWER 2.0/2.2 is detected as a USB device. After success-
ful automatic driver installation you can work with the qTOWER. If the drivers are not
installed automatically, you can complete the installation via the Windows routine.
The drivers are on the installation CD.
10. Start the qPCRsoft software.
11. If you have installed the color modules, specify them in the qPCRsoft software (→
see section "Installing color modules" p. 23).
12. Retain the transport packaging for subsequent transports.
The qTOWER 2.0/2.2 is now ready for use. Its operation is software-
controlled using qPCRsoft. Additional configurations for the measuring or
temperature program can be found in the software component of the oper-
ating manual.
Alternatively to completely shutting down the qTOWER 2.0/2.2 from the mains switch, it can
also be put into sleep mode. This interrupts the communication with the PC and the soft-
ware.
Touch the touch sensor at the front of the qTOWER 2.0/2.2 until it illuminates red.
This interrupts the communication to the PC.
Caution:
In sleep mode the qTOWER 2.0/2.2 is not switched off completely and continues to draw
current.
IMPORTANT
If sleep mode is not desirable, it can be disabled with the "standby" bridging switch on the
backplate of the device. To this end move the "standby" switch to the "1" position.
The qTOWER 2.0/2.2 will then only be switched off and on via the mains switch.
Fig. 8 Schematic representation of the position of additional vessels in case of low sam-
ple numbers
1. Prepare a real-time PCR project with complete details about the PCR run, fluorescence
measurements and the sample layout of the PCR plate (see qPCRsoft manual).
2. Open the lid by pressing in the red handle on the front until the lock opens with a click.
Fold back the upper part of the device.
3. Place the PCR plates onto the thermal block in such a way that well A1 is on the left-
hand side (arrow in the figure below). This position also corresponds to the well alloca-
tion in the qPCRsoft program.
4. Fold the lid forward and press it down from the handle until the lock engages with a
click.
5. Start the PCR run in the qPCRsoft program.
CAUTION
The use of solvents can damage the paintwork.
Proceed as follows:
1. Switch off the qTOWER 2.0/2
2. Open the lid and remove the four external
screws on the inside of the lid.
3. Close the lid again.
16. Switch on the qTOWER 2.0/2.2 and start the qPCRsoft software.
17. Open the menu command EXTRAS / EDIT COLOR MODULES.
The window with the same name opens.
On the left-hand side all color modules available for your device are displayed.
18. From the list select the module you have installed in the device, enable the checkbox
PROPERTIES and select the position on which you have installed the module in the de-
vice. If necessary, add dye names, if these have not yet been included in the list.
Click on [ACCEPT].
19. Proceed in accordance with the instructions in item (16) for each color module you
have installed.
20. If you want to define a new color module which is not included in the list of available
color modules, click on [ADD]. A new color module with the name COL-
OR.000.000.00.0 is created whose properties you can define on the right-hand side
of the dialog.
21. You can remove a color module from the list by highlighting it with the cursor and
then clicking on [DELETE].
22. You can modify the properties of a color module as follows:
− Enable the PROPERTIES checkbox.
− In the list POSITION select the position of the color module on the carrier in the
fluorescence measuring head.
− In the input field CODE OF MODULE enter the code noted on the color module.
− Enter the dye to be detected by the color module.
Click on [+].
The dye is added to the list below.
You can remove a dye by highlighting it in the list and clicking on [-].
23. Click [ACCEPT] to assign the properties to the marked color module.
IMPORTANT
The qTOWER 2.0/2.2 is only protected against transport damage if the packaging instruc-
tions are adhered to and the device is secured between the plastic sheets. Analytik Jena is
not liable for transport damage due to incorrect packaging.
8.2 Returns
CAUTION! PERFORM PROFESSIONAL DECONTAMINATION!
Before returning your device to Analytik Jena AG perform a professional decontamination!
Please clean all device components from biologically hazardous, chemical and radi-
oactive contamination.
Copy the decontamination declaration in section "Decontamination certificate" p.30,
complete it and attach the decontamination declaration to the outside of the ship-
ment.
Only use the original packaging for the shipment. If this is no longer available, please
contact Analytik Jena AG or your local dealer.
Please attach the warning note "CAUTION! SENSITIVE ELECTRONIC DEVICE!" to
the packaging.
Please include a sheet containing the following data:
− Name and address of the sender
− Name and telephone number of a contact for inquiries
− A detailed description of the fault, the precise conditions and situations under
which the fault occurs
IMPORTANT
If a contaminated device arrives at Analytik Jena AG, we must refuse acceptance. The
sender of the item may be liable for any damage caused by inadequate decontamination of
the device.
Observe the following when moving the device within the laboratory:
Disconnect the mains connection and the PC from the device.
To prevent health damage the following must be observed when moving the device
in the laboratory (lifting and carrying):
− For reasons of safety 2 persons are required to transport the device and must
position themselves on both sides of the equipment.
− Since the device does not have handles, grip the device firmly with both hands at
the lower end, lifting it simultaneously.
Observe the guide values and adhere to the legally mandated limits for lifting and
carrying without auxiliary means!
For installation at the new location observe the notes in section "Site requirements" p. 15.
8.4 Storage
CAUTION
Environmental influences and condensation can destroy individual components of the
qTOWER 2.0/2.2!
The device must only be stored in air-conditioned rooms. The atmosphere must be low in
dust and free from aggressive vapors.
If the device is not installed immediately after delivery or not required for prolonged periods,
it should be stored in its original packaging. A suitable desiccant should be added to the
equipment to prevent damage from moisture.
The following requirements are placed on the climatic conditions in the storage room of the
analyzer:
Temperature range: +5 °C to +55 °C
max. humidity: 10 % to 30 %
Air pressure: 0.7 bar to 1.06 bar
9 Decontamination certificate
To prevent endangering employees during repair or maintenance please complete and con-
firm the following. We make specific reference to
article 71 radiation protection ordinance, article 17 hazardous substances ordinance and
article 19 Law on chemical substances.
COMPANY / INSTITUTE
_________________________________________________________________________
ADDRESS
_________________________________________________________________________
EMAIL __________________________________________________________________
_____________________ _____________________
This signature confirms that the product is free from contamination. If the decontamination has been performed
insufficiently, this signature confirms acceptance that the resulting consequential costs (e.g. decontamination by a
specialist company or disposal of the product as radioactive waste by a specialist company) is borne by the origina-
tor.
Send this form together with the product to Analytik Jena AG or your field representative of
Analytik Jena AG.
Attach this completed form to the outside of the packaging. Products without this
form are returned to the sender at his own cost.
10 Disposal
The operator of the qTOWER 2.0/2.2 must dispose the waste materials arising during meas-
urements (sample materials) in accordance with the statutory and local regulations.
Dispose of the device and its electronic components in accordance with the applicable regu-
lations as electronic waste after its service life has expired.