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, allowing詳細を見る
製品番号(カタログ番号)数量
44856891 system
製品番号(カタログ番号) 4485689
価格(JPY)
-
見積もりを依頼する
数量:
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.
研究用途にのみご使用ください。診断目的には使用できません。
仕様
概要QuantStudio™ 6 Flex Real Time PCR System, 96-well
ディスプレイタイプTouchscreen
使用対象 (装置)QuantStudio™
フォーマット96-well Plate
製品ラインQuantStudio
数量1 system
ブロックフォーマットInterchangeable
Unit SizeEach
組成および保存条件
Laptop Computer

よくあるご質問(FAQ)

QuantStudio 6 and QuantStudio 7の違いはなんですか

主な違いは、使用可能なブロックとフィルターの種類です。

QuantStudio 6 ブロック: 96, 96 Fast, 384
QuantStudio 7 ブロック: 96, 96 Fast, 384, 384 well TaqMan® Array Card
QuantStudio 6 フィルター: 5 色
QuantStudio 7 フィルター: 6 色 (組み合わせ21 通り)

ライセンスが切れているかどうか、どこで確認ができますか?

ソフトウェアを開き、Tools --> License Centralから、ライセンスステータスおよび、有効期限が確認できます。

ライセンスの更新はどのように行えばよいでしょうか?

ライセンス更新手順が以下のサイトに掲載されております。
ライセンス更新手順 
手順に従い、更新作業を行ってください。ご不明点がございましたら、テクニカルサポートまでお問い合わせください。

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.

引用および参考文献 (3621)

引用および参考文献
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