Cytomètre de flux CytoFLEX

Le cytomètre de flux CytoFLEX, première version de la plate-forme CytoFLEX, est facile à utiliser et apporte les performances indispensables permettant de se concentrer sur l’analyse et pas sur l'instrumentation. Sa sensibilité et sa haute résolution, quelle que soit la configuration, lui donnent un avantage considérable sur des cytomètres quatre fois plus gros.

La série Violet-Bleu-Rouge (V-B-R), entièrement activée pour 13 couleurs ou seulement active pour quatre couleurs mais avec la possibilité d’activer des canaux supplémentaires ultérieurement
13 filtres passe-bande: 450/45, 525/40 (2), 585/42, 610/20 (2), 660/10 (2), 690/50, 712/25, 780/60 (3)
Un chargeur de plaques est disponible en option pour les applications à débit plus élevé, et pour une utilisation dans des environnements réglementés, le logiciel contient des outils de conformité 21 CFR Part 11.

Fonctionnalités

Sensibilité excellente

Conçu à partir de technologies innovantes, il offre des capacités de détection exceptionnelles
Large dynamique permettant de résoudre les problèmes de populations faiblement et fortement positives dans le même échantillon
Utilise la dispersion latérale violette pour détecter les nanoparticules

Polyvalence de la plateforme

Achetez le nombre de paramètres nécessaires maintenant
Ajouter davantage de paramètres en achetant une clé d'activation
Comprend une gamme complète de filtres passe-bande repositionnables, des filtres non standard sont également disponibles pour encore plus de flexibilité

Faible entretien

Les lasers, l’optique et la cellule de flux sont tous montés sur un socle isolé des vibrations, qui maintenant l’alignement optique.
Système fluidique basse pression
La maintenance préventive peut être effectuée par l'utilisateur, aucune visite de maintenance n'est requise.

Automatisation

Chargeur d'échantillons de plaque à 96 puits en option
API (Application Programming Interface) permet à un logiciel externe de contrôler l’instrument
Intégration de l’instrument Biomek i-Series pour le traitement automatisé des échantillons et l’acquisition de données

Caractéristiques

Detection	Photodiodes
Resolution	<300 nm particles (488 nm side scatter), <80 nm polystyrene particles (405 nm side scatter), rCV 3%
Performance	<30 MESF for FITC, <10 MESF for PE
Flow Cell	Patent-pending, alignment-free integrated optics quartz flow cell (420 μm x 180 μm ID) design with >1.3 numerical aperture
Signal Processing	Digital system with 7-decade display

Power Requirements	100-240 VAC, 50/60 Hz
Item Specifications Referenced	B53000

Documentation

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Title	Description
BeckmanConnect Installation and Activation Instructions {B14306BD-BB46-4B27-BF3E-B11862085BC7}	A step-by-step guide to help you successfully install BeckmanConnect.
Tech Note: Violet Side Scatter Use in Nanoparticle Detection {749D68FB-4893-4B2D-BD6C-C662F0520F64}	How to Use Violet Side Scatter to Detect Nanoparticles on the CytoFLEX Flow Cytometer
CytoFLEX System Performance Evaluation {C00ACFAF-8661-4DF6-8BA5-A7A099A7BA9C}	Authors: James Tung, Dan Condello, Albert Donnenberg, Erika Duggan, Jesus Lemus , John Nolan, Kathy Ragheb, Jennifer Sturgis, J Paul Robinson, Zhao, Jing, Domenic Fenoglio, Yijun, Huang, Paul Scibelli \| Beckman Coulter, Miami FL, Purdue University Cytometry Laboratories, La Jolla Bioengineering Institute, University of Pittsburgh Cancer Center, Sun Yat-Sen University, School of Medicine, Guangzhou, China
Quality Assurance for your CytoFLEX Flow Cytometer {A0D0EF0B-43F2-431C-BEB0-69F98765BDC4}	Paramount for any lab is consistent accurate data. Proper instrument performance is central to achieving this.
Fully-Automated Cellular Analysis by Flow Cytometry Poster {C00ACFAF-8661-4DF6-8BA5-A7A099A7BA9C}	The Biomek i7 Automated Workstation was used to automate the complete cellular workflow for induction and analysis of apoptosis in two cancer lines
Manufacturing Processes for Engineered T-Cell Therapy – CAR-T	Brochure presenting the CAR-T cell therapy workflow and associated product portfolio
Complete Solutions for your Specific Exosome Workflow from Preparation to Analysis {749D68FB-4893-4B2D-BD6C-C662F0520F64}	Beckman Coulter provides solutions customized for each step in your specific exosome research workflow – from sample preparation to sample analysis – and can also help improve processes and assist with related challenges.
Advanced Analysis of Human T Cell Subsets on the CytoFLEX Flow Cytometer using a 13 Color Tube Based on DuraClone Dry Reagent Technology {749D68FB-4893-4B2D-BD6C-C662F0520F64}	Authors: Nicole Weit, Michael Kapinsky, and Andreas Böhmler \| Beckman Coulter GmbH, Krefeld, Germany and Beckman Coulter Immunotech S.A.S, Marseille, France \| Published 2015
BeckmanConnect Security Highlights {749D68FB-4893-4B2D-BD6C-C662F0520F64}	This document highlights the privacy and security features in the BeckmanConnect remote management solution.
High Content DuraClone Reagents on the CytoFLEX Flow Cytometer: Instrument Setup using the CytoFLEX Compensation Library {E588CF40-730C-4137-A5DC-8DDEAB7CF7D9}	Authors: Dr. Nicole Weit, Dr. Andreas Böhmler, Dr. Michael Kapinsky \| Published 2015
CytoFLEX System Performance Evaluation {E588CF40-730C-4137-A5DC-8DDEAB7CF7D9}	Performance testing of cytometry instruments is utilized to characterize the capability of the cytometer to perform high complexity applications
Protection Plan for your Workflows in Flow Cytometry {9E29D7A5-B5EC-470A-A5C1-4EF9BFAE9959}	Maintenance service plan for Beckman flow analyzers.
Flow Cytometry Training {9E29D7A5-B5EC-470A-A5C1-4EF9BFAE9959}	Real-world training programs to maximize the value of your flow cytometer investment.
CytoFLEX Flow Cytometer Platform Brochure {A7DF4F56-8AF9-4BF1-88BE-766AB73FBC6B}	Provides an overview of all three models and describes the unique collection of technologies that contribute to the sensitivity of the platform
CytoFLEX Instrument Evaluation Using Biological Specimens {C00ACFAF-8661-4DF6-8BA5-A7A099A7BA9C}	Authors: James Tung, Dan Condello, Albert Donnenberg, Erika Duggan, Jesus Lemus, John Nolan, Kathy Ragheb, Jennifer Sturgis, Paul Scibelli, J Paul Robinson, Domenic Fenoglio \| Beckman Coulter, Miami FL, Purdue University Cytometry Laboratories, La Jolla Bioengineering Institute, University of Pittsburgh Cancer Center
Specification Sheet: CytoFLEX S Series N-V-B-R {B14306BD-BB46-4B27-BF3E-B11862085BC7}	Technical Specifications for the CytoFLEX S Near UV-Violet-Blue-Red (N-V-B-R) Series of flow cytometers
Specification Sheet: CytoFLEX Series V-B-R {B14306BD-BB46-4B27-BF3E-B11862085BC7}	Technical Specifications for the CytoFLEX Violet-Blue-Red (V-B-R) Series of flow cytometers
Specification Sheet: CytoFLEX S Series V-B-R-I {B14306BD-BB46-4B27-BF3E-B11862085BC7}	Technical Specifications for the CytoFLEX S Violet-Blue-Red-Infrared (V-B-R-I) Series of flow cytometers
Specification Sheet: CytoFLEX LX Series N-V-B-Y-R-I {B14306BD-BB46-4B27-BF3E-B11862085BC7}	Technical Specifications for the CytoFLEX LX Near UV-Violet-Blue-Yellow Green-Red-Infrared (N-V-B-Y-R-I) Series of flow cytometers
Specification Sheet: CytoFLEX LX Series U-V-B-Y-R-I {B14306BD-BB46-4B27-BF3E-B11862085BC7}	Technical Specifications for the CytoFLEX LX UV-Violet-Blue-Yellow Green-Red-Infrared (U-V-B-Y-R-I) Series of flow cytometers
Specification Sheet: CytoFLEX S Series V-B-Y-R {B14306BD-BB46-4B27-BF3E-B11862085BC7}	Technical Specifications for the CytoFLEX S Violet-Blue-Yellow Green-Red (V-B-Y-R) Series of flow cytometers
Specification Sheet: CytoFLEX S Series N-V-B-Y {B14306BD-BB46-4B27-BF3E-B11862085BC7}	Technical Specifications for the CytoFLEX S Near UV-Violet-Blue-Yellow Green (N-V-B-Y) Series of flow cytometers
【カタログ】コンパクトフローサイトメーター CytoFLEX Family {A7DF4F56-8AF9-4BF1-88BE-766AB73FBC6B}	CytoFLEXファミリーは、最適なレーザー励起と蛍光検出系により最小の光ロスと高感度を実現した革命的なコンパクトフローサイトメーターです。電気通信の先進技術を採用し、進化を続けるCytoFLEXファミリーは、研究者の細胞解析における選択肢を拡げます。
Whitepaper: Support for Compliance with 21 CFR Part 11 Electronic Records: CytoFLEX Flow Cytometers with CytExpert 2.3 Software {E588CF40-730C-4137-A5DC-8DDEAB7CF7D9}	Provides a table referencing the regulation along with the specific software features that facilitate compliance with that section of the law
CytExpert for CytoFLEX Gain Independent Compensation Flyer {9E29D7A5-B5EC-470A-A5C1-4EF9BFAE9959}	Gain Independent Compensation, a feature of CytExpert acquisition software, is enabled by Avalanche Photodiode detectors and facilitates simplified workflows for immunophenotyping
CytExpert 2.3.0.84 Software Release Notes {749D68FB-4893-4B2D-BD6C-C662F0520F64}	CytExpert 2.3.0.84 Software Release Notes
Flow Cytometric Analysis of Auto-fluorescent Cells in Marine Demosponge Application Note {442DF88C-CA7F-4B78-AF75-9D2B985534C0}	Natural autofluorescence of marine organisms can be detected in flow cytometers. Utilizing this, an assay to assess aggregation and reorganization of the sponge is described.
Calcium Flux Assay by Flow Cytometry Application Note {442DF88C-CA7F-4B78-AF75-9D2B985534C0}	The unique peristaltic sample delivery system of the CytoFLEX analyzer enables optimized measurements of transient changes in intracellular calcium in cells following agonist activation.
Measuring Proliferation in Leukemia Cell Lines Using CFSE Application Note {442DF88C-CA7F-4B78-AF75-9D2B985534C0}	Carboxyfluorescein succinimidyl ester (CFSE) is a fluorescent cell staining dye which is cell permeable. It binds covalently to intracellular proteins. Fluorescence decreases over time as the dye is divided between daughter cells at each division. In this application note a detailed protocol for using this assay to assess cytotoxic effects of a pharmacologic agent is described.
Using Flow Cytometry to Assess Protein Aggregation in Bacterial Overexpression Systems Application Note {442DF88C-CA7F-4B78-AF75-9D2B985534C0}	Describes the use of Proteostat dye in a flow cytometric assay for detection of aggregated protein in bacteria inclusion bodies. This assay can be used to assess bacterial culture conditions that favor production of soluble protein. This method reduces the amount of sample preparation required compared to gel electrophoresis-based methods.
Competitive Mouse Bone Marrow Transplantation Reconstitution Assay Application Note {442DF88C-CA7F-4B78-AF75-9D2B985534C0}	Using primary-conjugated antibodies against CD45.1 and CD45.2, we measure competitive bone marrow transplantation success by quantifying the proportion of donor cells (marked by CD45.1/Ly5.1 expression) and recipient cells (marked by CD45.2/Ly5.2 expression) in the peripheral blood of irradiated recipient mice post-transplantation.
Identifying Brain Tumor Initiating Cells Using Flow Cytometry Application Note {442DF88C-CA7F-4B78-AF75-9D2B985534C0}	Tumors represent a heterogenous population. Enumerating cells with stem cell like properties via co-expression of markers provides insight into the evolution of the tumor over time and throughout treatment. Detailed procedure for processing brain tissue for culture and flow cytometric analysis is provided.
Characterizing T Helper Cells Populations by Intracellular Cytokine Expression Using Flow Cytometry Application Note {442DF88C-CA7F-4B78-AF75-9D2B985534C0}	T helper cells are distinguished functionally by their cytokine profile, their major effector molecules. This application note provides a procedure for assessing the cytokine profile using flow cytometry and demonstrates T Helper cell subtypes Th1, Th2, Th17 and a non-classic Th1 type.
Using Cell Impermeant DNA Binding Dyes for Viability Assessment in Multicolor Flow Cytometry Application Note {442DF88C-CA7F-4B78-AF75-9D2B985534C0}	Compares viability staining using DRAQ7, DAPI, and 7-AAD in a multicolor immunophenotyping panel. Attributes of each dye are evaluated to aid in selection during panel design.
Phenotypic Characterization of Human Natural Killer Cell Populations in Peripheral Blood Application Note {442DF88C-CA7F-4B78-AF75-9D2B985534C0}	Describes a 10 color, 13 marker panel to investigate the NK cell population, both phenotypically and functionally in human PBMC samples. The panel includes the use of an exclusion markers on a dump channel used to gate out non-NK cells. Deep phenotyping markers for the NK cell compartment are included and a comprehensive gating strategy is defined.
Identifying Discrete Mouse Splenocyte and Peripheral Blood Cell Subpopulations Using Surface Markers Application Note {442DF88C-CA7F-4B78-AF75-9D2B985534C0}	Flow cytometry is extremely useful for detecting cell surface antigen expression, and thereby facilitates the characterization, identification, and isolation of discrete cell populations within heterogeneous samples. We describe a method to rapidly isolate and delineate CD3ε-positive T cell and CD19-positive B cell populations from murine spleen and peripheral blood samples.
Plant Genome Analysis by Flow Cytometry {442DF88C-CA7F-4B78-AF75-9D2B985534C0}	Provides a detailed protocol for preparing nuclei from plant tissues. DNA in the nuclei is then stained with propidium iodide and the flow cytometer is used to assess DNA content. Values obtained are then correlated with the Kew Database to assess ploidy. This assay can be used to investigate the role of endoreplication in plant development across species.
Flow Cytometric Approach to Probiotic Cell Counting and Analysis Application Note {442DF88C-CA7F-4B78-AF75-9D2B985534C0}	Describes a staining procedure and instrument set up for absolute counting of probiotic bacterial culture. A workflow comparison with the traditional plate-based assay as well as correlated cell counts are provided.
Identification of Natural Killer Cells in Rat Placenta Model of Preeclampsia Using Flow Cytometry Application Note {442DF88C-CA7F-4B78-AF75-9D2B985534C0}	A special population of natural killer cells (uNK) has been implicated in preeclampsia. uNK cells have contact with the trophoblast, modify uterine arteries to promote blood flow, and modulate trophoblast invasion in a dose-dependent manner. In this application note a detailed method for preparing resident NK cells from tissue and an assay to access NK cell activation is provided.
Phagocytosis of Bacteria in a Whole Blood Assay Application Note {442DF88C-CA7F-4B78-AF75-9D2B985534C0}	Describes an opsonization assay which can be used to assess the phagocytic capabilities of immune cell in whole blood. The benefits of using multicolor flow cytometry for the assay is that different phagocytic potential across various immune cell types can be determined in the same sample.
Thirteen Color Immunophenotyping T Cell Subsets in Whole Blood Application Note {442DF88C-CA7F-4B78-AF75-9D2B985534C0}	Contains a comprehensive overview of T cell biology and the implications for multicolor immunophenotyping panel design. Includes a detailed gating strategy for deep immunophenotyping of T cell populations including rare cell types. Also includes step-by-step instructions for setting up the CytoFLEX for multicolor immunophenotyping including use of the Compensation Library.
Red Blood Cell Microparticle Analysis by Flow Cytometry Application Note {442DF88C-CA7F-4B78-AF75-9D2B985534C0}	Discover how to stain microparticles for flow cytometric analysis. The assay describes sample preparation, staining, and gating steps to distinguish red blood cell-derived microparticles from microparticles from other tissue origins. Representative data from several replicates are provided in order to report out precision obtainable from this approach.
How to use VSSC on CytoFLEX Technical Note {749D68FB-4893-4B2D-BD6C-C662F0520F64}	The purpose of this paper is to demonstrate how to setup the CytoFLEX flow cytometer to detect small particles by Violet Side Scatter (VSSC). A bead mixture is defined to assist in demonstrating the detection capabilities. Using VSSC, the CytoFLEX was able to clearly discriminate 80 nm polystyrene and 150 nm silica nanoparticles from background noise.
Single Cell Analysis of Autophagy Application Note {442DF88C-CA7F-4B78-AF75-9D2B985534C0}	Provides a detailed procedure for using the Cyto-ID Autophagy kit in a flow cytometry assay. Contains background information on the physical and chemical hallmarks of autophagy and the benefits of a single cell assay versus bulk analysis of this biological process.
Assessing T Cell Subpopulations by TCR Expression in PBMCs Application Note {442DF88C-CA7F-4B78-AF75-9D2B985534C0}	We outline a protocol using DURAClone™ IM panels, which are unitized, dry format, room temperature stable reagent cocktails, to delineate and quantify T cell subpopulations from a heterogeneous sample of isolated normal PBMCs based on TCR composition.
Nano- and Microparticle Bead Mix for Use as a Sizing Standard in Flow Cytometry {C00ACFAF-8661-4DF6-8BA5-A7A099A7BA9C}	The CytoFLEX platform is distinguished for not only its fluorescence sensitivity but also its ability to detect in the nanoparticle range using Violet Side Scatter. This poster, presented at Cyto in 2016 describes a NIST-traceable bead mix for use in standardizing flow cytometry experiments.
Resolving Dyes with Identical Emission Wavelengths on the CytoFLEX {C00ACFAF-8661-4DF6-8BA5-A7A099A7BA9C}	Compensation in flow cytometry is a special case of spectral deconvolution. In this poster we demonstrate that the CytoFLEX can deconvolute highly overlapping fluorophores using the compensation algorithm.
Preparing a CytoFLEX for Nanoscale Flow Cytometry {C00ACFAF-8661-4DF6-8BA5-A7A099A7BA9C}	In this poster, we will demonstrate how to properly setup and clean a CytoFLEX flow cytometer for NP analyses
Twenty-seven Markers on a 3-laser Flow Cytometer {C00ACFAF-8661-4DF6-8BA5-A7A099A7BA9C}	This poster was presented at Cyto in 2018 and demonstrates a technique to maximize the usage of channels on a flow cytometer. The method relies on stacking biomarkers that are not expressed on the same cell and a gating technique to interrogate the populations of interest.
CytoFLEX Instrument Set-up for Measuring Extracellular Vesicles Application Note {442DF88C-CA7F-4B78-AF75-9D2B985534C0}	Describes the instrument set up and verification steps required for measuring extracellular vesicles by flow cytometry. Instructions for reducing background particles found in buffers and reagents to enhance small particle detection.
A Prototype CytoFLEX for High-Sensitivity, Multiparametric Nanoparticle Analysis {C00ACFAF-8661-4DF6-8BA5-A7A099A7BA9C}	In this poster, we will demonstrate the VSSC-based size resolution and fluorescence sensitivity of our prototype using a variety of NIST-traceable size standards and fluorescent nanoparticles
Characterizing the Light-Scatter Sensitivity of the CytoFLEX Flow Cytometer {C00ACFAF-8661-4DF6-8BA5-A7A099A7BA9C}	The CytoFLEX is so sensitive that the SSC detector actually has an attenuation filter to reduce 95% of the scatter signal, adjusting it to a range useful for cells
Using Violet Side Scatter to Detect and Resolve Nanoparticles on the CytoFLEX Flow Cytometer {C00ACFAF-8661-4DF6-8BA5-A7A099A7BA9C}	This poster provides detailed instructions for setting up the CytoFLEX flow cytometer Violet Side Scatter for nanoparticle detection. Experimental considerations for nanoscale flow cytometry and illustrated with data from the instrument.
Identification of Circulating Myeloid Cell Populations in NLRP3 Null Mice Application Note {442DF88C-CA7F-4B78-AF75-9D2B985534C0}	In this case study, using the surface markers Ly6C (hematopoietic precursor cells, monocytes), Ly6G (granulocytes/neutrophils), and CD115 (macrophage colony-stimulating factor [M-CSF] receptor; macrophages), we examined and identified the differences in circulating cell populations in fresh blood samples.
Eight Color Immunophenotyping Unlysed Whole Blood Application Note {442DF88C-CA7F-4B78-AF75-9D2B985534C0}	This whole blood assay does not involve harsh lysis or centrifugation steps, minimizing any cell perturbations from sample handling. This 8-color panel provides a broad survey of peripheral blood leukocytes.
Flow Cytometric Quantification to Assess Doral Endocytosis Application Note {442DF88C-CA7F-4B78-AF75-9D2B985534C0}	This application note demonstrates the use of flow cytometry to examine the phagocytosis of collagen type I-coated fluorescent microspheres by rat embryonic fibroblasts. Cellular uptake can be assessed quickly in a large number of cells using flow cytometry.
Ten Color Immunophenotyping of Mouse NK Cells Application Note {442DF88C-CA7F-4B78-AF75-9D2B985534C0}	Surface-marker expression is critical to the delineation of NK cell maturity, function, and localization. We present a protocol and gating strategy for the identification of splenic murine NK cell populations via the CytoFLEX flow cytometer using a 10-color screen.
CytoFLEX Quick User Guide {B14306BD-BB46-4B27-BF3E-B11862085BC7}	This document gives step by step instructions on how to operate CytoFLEX
Absolute Counting using the CytoFLEX {E588CF40-730C-4137-A5DC-8DDEAB7CF7D9}	In this whitepaper we compare and contrast syringe-based and peristaltic pump-based fluidics system for the application of beadless absolute counting. Topics important to the validation of a counting assay are discussed.