QuantStudio™ 6 Flex Real-Time PCR System, 96-well, laptop
QuantStudio™ 6 Flex Real-Time PCR System, 96-well, laptop
Applied Biosystems™

QuantStudio™ 6 Flex Real-Time PCR System, 96-well, laptop

The Applied Biosystems® QuantStudio™ 6 Flex Real-Time PCR System facilitates real-time PCR based applications with an upgradable block selection, allowingMás información
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44856891 system
Número de catálogo 4485689
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1 system
The Applied Biosystems® QuantStudio™ 6 Flex Real-Time PCR System facilitates real-time PCR based applications with an upgradable block selection, allowing you to plan for experiments today and grow with tomorrow’s needs. With a simplified workflow, intuitive software, and touch-screen interface, the QuantStudio™ 6 Flex system offers exceptional reproducibility at a price you can afford.

Features of the QuantStudio™ 6 Flex Real-Time PCR System include:

• Affordable price allows you to obtain a high performance instrument with minimal upfront capital investment
• Compatible with over 8 million TaqMan® assays for gene expression, genetic variation, gene regulation, or protein expression experiments
• The intelligent design of the QuantStudio™ platform combined with Applied Biosystems® instrument reliability and accuracy
• Easy-to-use software, responsive touch-screen, and effortless block exchange without the need for any tools

Thermo Fisher Cloud
Thermo Fisher Cloud provides scientists with a secure place to store, analyze, and share data. Applied Biosystems qPCR Analysis Modules within the Thermo Fisher Cloud are web browser-based software tools that are flexible, fast and easy to use. These software tools are compatible with Mac or PC as well as most Applied Biosystems instrument file types.

>> Download a 90-day trial of the QuantStudio™ 6 software

The QuantStudio™ 6 Flex system accommodates the interchange of a 96-well, 96-well Fast, or 384-well block. The system is delivered with one block type (a 96-well block in this case); other block types may be purchased separately. For a system that also supports TaqMan® array cards, as well as automation, please see our QuantStudio™ 7 Flex system. The QuantStudio™ 6 Flex system can also be upgraded to a QuantStudio™ 7 Flex system at a later date, as your needs change. For the ultimate in productivity, consider the QuantStudio™ 12K Flex system, which also accommodates TaqMan® OpenArray® plates.

Upgrade Capabilities When You Need Them

The QuantStudio™ 6 Flex system can be seamlessly upgraded to a QuantStudio™ 7 Flex system by a field service engineer to give you additional automation, throughput, and multiplexing capabilities.

Results You Can Trust
Improved well-to-well and instrument-to-instrument data accuracy is achieved with the OptiFlex® system, which features 5 coupled excitation and emission filter channels.

Sensitive Data Analysis
Detect changes in target quantity as small as 1.5-fold in single-plex reactions and obtain 10 logs of linear dynamic range.

Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.

Especificaciones
DescripciónQuantStudio™ 6 Flex Real Time PCR System, 96-well
Tipo de pantallaTouchscreen
Para utilizar con (equipo)QuantStudio™
Formato96-well Plate
Línea de productosQuantStudio
Cantidad1 system
Formato de bloqueIntercambiables
Unit SizeEach
Contenido y almacenamiento
Ordenador portátil

Preguntas frecuentes

How do I activate or renew my software license in the QuantStudio 6 or QuantStudio 7 Real-Time PCR System?

Please follow the instructions found in the Software Licensing Quick Reference Guide at https://fnoclient.gss.tf/quick-start-guide to activate or renew a license for the QuantStudio 6 or QuantStudio 7 Real-Time PCR System. If you have a license key associated with a computer that is no longer in use, please follow the instructions to "Transfer a license to a different user or computer" in the above guide.

Find additional tips, troubleshooting help, and resources within our Real-Time PCR and Digital PCR Instruments Support Center.

What should I do if the software will not connect to the QuantStudio 6 or QuantStudio 7 Real-Time PCR System?

After launching the QuantStudio software, go to the Maintenance Manager. Check if the QuantStudio system icon is present in the “On the Network” window. If not, click on the ‘Refresh' button to the left of ‘Remove from My Instruments'. If you still do not see the QuantStudio system icon for the following reasons:

- There is an icon but you cannot add it into the "My Instruments" area
- There is a red “X” on the instrument
- A message says "Disconnected" at the bottom of the window with a red “X” in it
then you will need to add the Instrument into the ‘My Instruments' area. Click on the wrench icon in the upper right-hand corner of the icon as pictured below. You may get a message that says the firmware is older than the one you're trying to run. If appropriate, choose to download the new firmware and let it progress to finish. Do not turn off the instrument during this update. After the firmware update is completed, restart the instrument and check for the QuantStudio system icon in ‘On the Network' area.

Find additional tips, troubleshooting help, and resources within our Real-Time PCR and Digital PCR Instruments Support Center.

What can I do when I get an error message related to "...JVM..."?

This error can occur due to allocation of the computer's virtual memory. If you see this message, try the following:

1. Click ‘OK' to the error, close any unnecessary programs, and re-launch the software (you may have to do this several times).
2. Using the Task Manager (Control+Alt+Delete), look for a process called ‘javaw.exe'. Select this line and end the process. Then re-launch the software.

Find additional tips, troubleshooting help, and resources within our Real-Time PCR and Digital PCR Instruments Support Center.

On the QuantStudio 6 and 7 Flex instruments, what does the error “Calibration file already exists” mean?

The calibration files are stored on the QuantStudio 6/7 Flex instrument itself; therefore, when you need to perform a new calibration, you will have to delete the old calibration files. From the instrument console, go to the QuantStudio 6/7 Flex instrument touchscreen and select ‘Collect Results'. You should then see a list of files stored on the instrument. Manually select a calibration file such as “Fast-96-cal”, and press the ‘Delete' button to remove the old calibration file. Occasionally, users cannot delete the file off the instrument and may encounter this error: “Some experiments did not collect results therefore cannot be deleted.”. In these situations, launch the software, go to ‘maintenance', manage files, and download the calibration file. The status of the experiment should be displayed as ‘complete'. Next, delete the old calibration file and rerun the calibration.

Find additional tips, troubleshooting help, and resources within our Real-Time PCR and Digital PCR Instruments Support Center.

Is it possible to see the traces in an allelic discrimination experiment on the QuantStudio 6 and QuantStudio 7 Flex Real-Time PCR Systems?

The ‘reveal traces' feature for genotyping runs allows you to trace the clusters throughout the PCR process. For some assays you may find better cluster discrimination at, say, cycle 40, as opposed to cycle 50. To use this feature, the amplification data needs to have been collected for the run.

- Go to ‘Analysis Settings'
- Under the default ‘Call Settings' tab, Choose ‘Analyze Real-Time Rn Data'
- Click ‘Apply Analysis Settings'
- Under the Allelic Discrimination Plot, check the box next to ‘Reveal Traces'. You can then move the slide bar to see how the data changes with the cycles number.
In the example below, the image on the left shows the data at a full 40 cycles. The image on the right is the same data after revealing traces (grey lines). The clusters can be traced back by moving the cycle bar. Notice that one point is no longer called at the earlier cycle set point.

Find additional tips, troubleshooting help, and resources within our Real-Time PCR and Digital PCR Instruments Support Center.

Citations & References (3621)

Citations & References
Abstract
Identification of pathogenic TRAIL-expressing innate immune cells during HIV-1 infection in humanized mice by scRNA-Seq.
Authors:Cheng L,Yu H,Wrobel JA,Li G,Liu P,Hu Z,Xu XN,Su L
Journal:JCI insight
PubMed ID:32406872
Depletion of CD4(+) T cells during HIV-1 infection is mostly mediated by inflammatory cells via indirect but not clearly defined mechanisms. In this report, we used single-cell RNA-Seq (scRNA-Seq) technology to study HIV-induced transcriptomic change in innate immune cells in lymphoid organs. We performed scRNA-Seq on hCD45(+)hCD3(–)hCD19(–) human leukocytes isolated ... More
Development of a peptide drug restoring AMPK and adipose tissue functionality in cancer cachexia.
Authors:Ji H,Englmaier F,Morigny P,Giroud M,Gräsle P,Brings S,Szendrödi J,Berriel Diaz M,Plettenburg O,Herzig S,Rohm M
Journal:Molecular therapy : the journal of the American Society of Gene Therapy
PubMed ID:37408309
Cancer cachexia is a severe systemic wasting disease that negatively affects quality of life and survival in patients with cancer. To date, treating cancer cachexia is still a major unmet clinical need. We recently discovered the destabilization of the AMP-activated protein kinase (AMPK) complex in adipose tissue as a key ... More
Long noncoding RNA ENST00000455974 plays an oncogenic role through up-regulating JAG2 in human DNA mismatch repair-proficient colon cancer.
Authors:Lao Y,Li Q,Li N,Liu H,Liu K,Jiang G,Wei N,Wang C,Wang Y,Wu J
Journal:Biochemical and biophysical research communications
PubMed ID:30473216
Precisely controlling endogenous protein dosage in hPSCs and derivatives to model FOXG1 syndrome.
Authors:Zhu W,Zhang B,Li M,Mo F,Mi T,Wu Y,Teng Z,Zhou Q,Li W,Hu B
Journal:Nature communications
PubMed ID:30804331
Dosage of key regulators impinge on developmental disorders such as FOXG1 syndrome. Since neither knock-out nor knock-down strategy assures flexible and precise protein abundance control, to study hypomorphic or haploinsufficiency expression remains challenging. We develop a system in human pluripotent stem cells (hPSCs) using CRISPR/Cas9 and SMASh technology, with which ... More
Scrutiny of NolA and NodD1 Regulatory Roles in Symbiotic Compatibility Unveils New Insights into Bradyrhizobium guangxiense CCBAU53363 Interacting with Peanut (Arachis hypogaea) and Mung Bean (Vigna radiata).
Authors:Shang JY,Zhang P,Jia YW,Lu YN,Wu Y,Ji S,Chen L,Wang ET,Chen WX,Sui XH
Journal:Microbiology spectrum
PubMed ID:36475917
Bradyrhizobium guangxiense CCBAU53363 efficiently nodulates peanut but exhibits incompatible interaction with mung bean. By comparing the common nod region with those of other peanut bradyrhizobia efficiently nodulating these two hosts, distinctive characteristics with a single nodD isoform (nodD1) and a truncated nolA were identified. However, the regulatory roles of NodD1 ... More