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

Applied Biosystems® QuantStudio™ 6 Flex Real-Time PCR System은 업그레이드 가능한 블록 선택을 통해 real-time PCR 기반 어플리케이션을 용이하게 하므로, 현재자세히 알아보기
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카탈로그 번호수량
44856891 system
카탈로그 번호 4485689
제품 가격(KRW)
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수량:
1 system
Applied Biosystems® QuantStudio™ 6 Flex Real-Time PCR System은 업그레이드 가능한 블록 선택을 통해 real-time PCR 기반 어플리케이션을 용이하게 하므로, 현재 실험에 대해 계획하는 것은 물론, 미래의 요구사항도 충족시킬 수 있습니다. 단순한 workflow, 직관적인 소프트웨어, 터치스크린 인터페이스를 지원하는 QuantStudio™ 6 Flex 시스템은 저렴한 가격과 더불어 우수한 재현성을 제공합니다.

>> QuantStudio™ 6 소프트웨어의 90일 평가판 다운로드

QuantStudio™ 6 Flex 시스템은 96-well, 96-well Fast 또는 384-well 블록의 교환이 가능합니다. 이 시스템에는 한 가지 블록 유형(이 경우에 96-well 블록)이 제공되며, 다른 블록 유형은 별도로 구입할 수 있습니다. 자동화뿐 아니라 TaqMan® 어레이 카드도 지원하는 시스템은 QuantStudio™ 7 Flex 시스템을 참조하십시오. 또한, QuantStudio™ 6 Flex 시스템은 이후 사용자 요구사항 변경에 따라 QuantStudio™ 7 Flex 시스템으로 업그레이드할 수 있습니다. 최고의 생산성이 필요하다면, TaqMan® OpenArray® 플레이트를 수용하는 QuantStudio™ 12K Flex 시스템이 가장 적합합니다.

QuantStudio™ 6 Flex Real-Time PCR System의 특징:

• 가격이 저렴하여 최소의 선불 설비투자로 고성능 기기 구입 가능
• 유전자 발현, 유전적 변이, 유전자 조절 또는 단백질 발현 실험을 위한 800만개 이상의 TaqMan® 분석에서 사용 가능
• Applied Biosystems® 기기 안정성 및 정확성과 QuantStudio™ 플랫폼의 지능형 설계가 결합된 제품
• 사용이 쉬운 소프트웨어, 즉시 응답하는 터치스크린, 다른 장비가 필요하지 않은 간편한 블록 교환

필요에 따라 업그레이드할 수 있는 기능

QuantStudio™ 6 Flex 시스템은 추가 자동화, 처리량 및 멀티플렉싱 기능을 지원할 수 있도록 현장 서비스 엔지니어를 통해 QuantStudio™ 7 Flex 시스템으로 완벽하게 업그레이드될 수 있습니다.

신뢰할 수 있는 결과
5개의 결합된 여기 및 방출 필터 채널이 장착된 OptiFlex® 시스템을 통해 웰 간 및 기기 간 데이터 정확성이 보장됩니다.

민감한 데이터 분석
Single-Plex 반응에서 1.5배만큼 적은 표적 양의 변화를 검출하고 10 log의 선형 동적 범위를 확보합니다.
For Research Use Only. Not for use in diagnostic procedures.
사양
설명QuantStudio™ 6 Flex Real Time PCR System, 96-well
디스플레이 유형Touchscreen
용도(장비)QuantStudio™
형식96-well Plate
제품라인QuantStudio
수량1 system
블록 형식Interchangeable
Unit SizeEach
구성 및 보관
Laptop Computer

자주 묻는 질문(FAQ)

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.

인용 및 참조 문헌 (3621)

인용 및 참조 문헌
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