Any cell or particle in size from 0.2-50 µm can be assayed on the system.
The NovoCyte is available in four different models which have 1, 2, or 3 lasers and from 3 to 13 fluorescence channels.
Innovations in the optical layout, electronic signal processing and the obscuration bar design result in high sensitivity and resolution for both scattered light signals and fluorescence signals:
Forward/side scatter resolution: FSC: 0.5 µm; SSC: 0.2 µm
Fluorescence sensitivity: FITC < 75 MESF; PE < 50 MESF
<3% CV for chicken erythrocyte nuclei DNA content analysis.
The sample flow rate can be adjusted continuously in the range of 5-120 µL/min. The maximum sample processing rate is 35,000 events per second.
The flow core diameter can be varied 4.6 to 22.7µm, corresponding to the flow rate range of 5 to 120 µL/min. The software indicates the altered flow core diameter as you modify the flow rate.
The NovoCyte is able to record up to 10 million events (either total or within a gate of interest), up to 5 mL of sample volume, and/or up to 120 min for each sample acquisition.
The syringe pump aspirates from 10 to 100 µL for each sample acquired plus 20 µL of void volume.
The NovoCyte uses advanced electronics and data processing algorithms to provide 7 decades of dynamic range. This high dynamic range eliminates the need for laborious PMT adjustment before each experiment.
Startup and shutdown cleaning routines are performed automatically, eliminating the need for time-consuming manual cleaning or decontamination protocols.
Also, the NovoCyte utilizes sensors in the fluidic pathway to monitor the system status in real time. Abnormal working conditions are reported on the NovoExpress software and one-click automated procedures can be executed, including routines that will backflush, debubble, unclog, prime, rinse, or clean the fluidics system.
Finally, fluidics system filters and tubing components may easily be changed on a recommended schedule (bi-monthly or bi-yearly, depending on the component) using kits available from ACEA.
No. The NovoCyte can do direct absolute counting with no need for expensive reference counting beads. The high precision syringe pump guarantees an accurate volume of sample is dispensed.
The precision of the direct absolute counting is < 5% CV.
The sample injection probe (SIP) is washed automatically after each sample collection, minimizing the possibility of sample carryover (<0.1%).
All of the necessary reagents to QC and run the instrument are available from ACEA, including NovoCyte Instrument QC Particles, NovoFlow sheath fluid, NovoRinse solution and NovoClean solution.
The sheath fluid consumption rate is 6.25 mL/min.
• NovoCyte: W × D × H: 60 × 45 × 39 cm (23.6 × 17.7 × 15.4 in.)
• Fluidics Station (including reagent containers): W × D × H: 25 × 29 × 42 cm (10.0 ×11.4 × 16.5 in.)
• NovoSampler: W × D × H: 31 × 26 × 28 cm (12.2 ×10.2 × 11.0 in.)
The NovoExpress software includes an automatic QC function. Just prepare the QC beads and click the QC test button on the NovoExpress software. A QC report is automatically generated and the results are displayed after about 2 minutes. A Levey-Jennings plot for the mean and CV of specific parameters is provided to track the performance of the instrument over time. This simple procedure may be done on a daily basis.
The NovoExpress software contains all the tools you expect for collecting and analyzing your flow data, including a variety of plot types (dot, density [grey or pseudo-color], contour, and histograms). In addition, a drag-and-drop software templating function allows for rapid application of settings and analysis across multiple samples. A built-in cell cycle analysis function (Watson pragmatic model with customizable constraints) eliminates the need for third party software.
The NovoCyte is a digital system, allowing for compensation after data acquisition. The NovoExpress software allows for direct editing of the compensation matrix as well as a simple-to-use Quick Compensation sliding bar to quickly achieve proper compensation. Also, NovoExpress provides an Auto Compensation function: after collection of data for single-stained samples, the software automatically calculates the compensation matrix for you.
The NovoExpress software generates .ncf files by default. It includes the data, compensation matrix, acquisition settings and analysis templates.
Yes, NovoCyte data may be exported in FSC3.0 format for analysis on third party software such as FlowJo. Also, NovoCyte data may be exported as a CSV file for analysis with programs such as Microsoft Excel.
Yes, the NovoExpress software is able to import and analyze FCS3.0 files.
Yes. Simply right click on a dot plot/histogram, select “edit overlays”, and then choose the sample or gate of interest.
Yes, the NovoExpress software is provided with a cell cycle module based on the Watson pragmatic model. To use it, just click on the corresponding icon on the tool bar.
Autosampler / NovoSampler
The optional NovoSampler allows for use of standard 24- or 96-well microtiter plates (U/V/flat-bottom) as well as a 24 tube rack (provided by ACEA) for use with standard 12X75 mm tubes. The modular design of the NovoCyte autosampler allows for convenient installation and calibration without the need for special tools.
A 96 well plate can be processed automatically in less than 60 minutes, using a 10 uL acquisition volume from each well.
Yes. Mixing is performed by agitating the plate using customizable, user-defined cycles.
A user-defined rinse program (0-3 cycles) for cleaning the fluidic system and the sample injection probe ensures that carryover is negligible (<0.1% with 1 rinse cycle per well).
Videos: Product Overviews
Videos: Research Presentations
About this Webinar
DNA content analysis using flow cytometry is a powerful tool that can determine the effect of treatments on cell cycle and ploidy in particular relevance to tumours. However, how do you determine which DNA-binding dye to use? How do you accurately differentiate the different phases in the cell cycle in your population of cells? This webinar will teach the methods for cell cycle analysis with the following topics:
During this webinar, we will cover:
- Phases of a typical mammalian cell cycle
- Characteristics of Nucleic Acid Stains
- How to choose the right fluorochromes and properly prepare your cells
- DNA ploidy & tumours
Date: Thursday, December 21, 2017
Time: 8 AM SINGAPORE | 9 AM TOKYO | 4 PM PST (Dec. 20)
Date: Thursday, December 21, 2017
Time: 7 AM PST | 10 AM EST | 4 PM PARIS
About the Presenter
Stephanie Ting, M. Eng
Field Application Scientist – SE Asia, ANZ, HK&Macau, India,
ACEA Biosciences Inc.
Stephanie received her Masters in Mechanical Engineering from the University of Tokyo, Japan where she studied the effects of mechanobiological stimuli on the production of cartilage-like tissues using mesenchymal stem cells. Currently, she is the Field Application Scientist for SE Asia, ANZ, HK&Macau, and India.
Accurate measurements of intracellular Ca2+ concentrations allows for a more comprehensive understanding of Ca2+ regulated cell functions and signaling pathways. Ca2+ is an important molecule that affects a wide range of physiological and pathological processes. Unlike other secondary messengers, Ca2+ is not synthesized or metabolized, but stored and rapidly released by channels/pumps that maintain Ca2+ concentrations in distinct cellular compartments. Flow cytometry allows real time measurement of a calcium flux response utilizing fluorescent Ca2+ indicators which exhibit an increase in fluorescence upon binding to Ca2+. In this webinar we will discuss the basics of calcium flux measurements by flow cytometry, providing specific details on experiment setup, acquisition, and analysis on the NovoCyte flow cytometer.
Key topics to be covered:
1. Essentials of calcium measurements by flow cytometer
2. Calcium flux experimental setup and acquisition on the NovoCyte
3. Detailed analysis of calcium flux in a T cell line using calcium indicator dye Fluo-4/AM
Lauren Jachimowicz, Ph.D.
Application Development Scientist, ACEA Biosciences, Inc.
Lauren Jachimowicz received her PhD in Biological Science from the University of California, San Diego where she studied the role of the circadian clock genes in T cells. Currently, she is the Application Development Scientist for flow cytometry at ACEA Biosciences advancing flow cytometry into new fields of research.
At the CYTO 2017 meeting Dr. Adriano Rossi and Dr. Calum Robb from the University of Edinburgh described the development of a new flow cytometry-based assay for studying NETosis, a cell death process that occurs when stimulated neutrophils cast an extracellular web containing DNA, histones, and anti-bacterial proteins that ensnare/neutralize invading organisms. Using the NovoCyte® flow cytometer, they demonstrate the detection and quantification of neutrophil extracellular traps (NETs), as well as analysis of the regulatory mechanisms involved.
About this Webinar
Researchers and flow cytometry users spend a significant amount of time designing flow assay panels and analyzing their samples.
In this webinar, viewers will have the chance to learn about tools and recent developments in flow cytometry that simplify assay design and workflow. Our speakers will explore the capabilities of benchtop and cost-effective flow cytometry systems and the easiest way to design flow panels.
- Design and capabilities of a NovoCyte flow cytometer
- New features that simplify setup, acquisition, and analysis
- How to design multicolor fluorescent panels using FluoroFinder’s experiment design platform
- Tips for building better panels in less time
Garret Guenther, Ph.D.
Jeff Jensen, Ph.D.
Flow cytometry remains an essential tool for cell analysis. Although often relegated to specialized core facilities, flow cytometry instruments are in fact becoming increasingly commonplace in life science labs.
In this special webinar, viewers will have the chance to learn about recent developments in flow cytometry technology, including the emergence of lower cost, smaller flow cytometry options with the capability of analyzing multiple fluorescent colors. Our speakers will explore the design, development, and uses for smaller, more cost-effective flow cytometry systems in research labs. In this webinar, you will gain insights on:
- Design and development of the latest multicolor flow cytometry instruments
- Application of flow cytometry techniques for different experimental needs
- How analyzing multiple cellular parameters using different fluorescent colors can extend experimental possibilities
- How to effectively analyze and interpret your flow cytometry data sets
Paul K. Wallace, PhD
Roswell Park Cancer Institute
Paul Wallace has served since 2003 as Director of the Flow and Image Cytometry Department at the Roswell Park Cancer Institute (RPCI) in Buffalo, NY, where he is a Professor of Oncology. He is also an Associate Professor of Biotechnical and Clinical Laboratory Sciences at the University at Buffalo. His primary expertise and board certification is in the flow cytometric diagnosis of hematological malignancies.
Christopher Groves is a Senior Manager at MedImmune Inc., where he heads a keystone technology group challenged with expanding knowledge of disease mechanisms while also delivering innovative solutions in drug discovery and manufacturing that provide scientists access to cutting-edge technological capability.
William Telford, PhD
Experimental Transplantation and Immunology Branch, NCI-NIH
William Telford is the Head of the NCI-NIH Flow Cytometry core facility, which provides state-of-the-art flow cytometry as well as imaging technology and instrumentation to users in the research community.
Patrick C.H. Lo, PhD
Senior Editor, BioTechniques