Citómetro de flujo CytoFLEX LX

El citómetro de flujo CytoFLEX LX es una expansión de la plataforma CytoFLEX. Este modelo amplía las posibilidades de investigación, con hasta seis láseres y 21 parámetros de color. Seis láseres separados espacialmente permiten que los paneles se distribuyan a lo largo del espectro, reduciendo la interferencia y el solapamiento espectral.

Hay dos series disponibles, UV-violeta-azul-amarillo verde-rojo-IR (U-V-B-Y-R-I) y UV cercano-violeta-azul-amarillo verde-rojo-IR (N-V-B-Y-R-I)
Están disponibles instrumentos con tan solo cuatro láseres activados y 14 parámetros del color, con la opción de activar láseres y colores adicionales en el futuro con la compra de una clave de activación
Para aplicaciones de mayor productividad está disponible un módulo cargador de placas opcional y para su uso en entornos regulados, el software contiene herramientas para el cumplimiento de la norma 21 CFR Parte 11

Características del citómetro de flujo CytoFLEX LX

Sensibilidad exquisita

Una combinación única de tecnologías innovadoras proporciona capacidades de detección excepcionales
Gran intervalo dinámico para resolver poblaciones tenues y brillantes en la misma muestra
Utilice la dispersión lateral violeta para detectar nanopartículas

Versatilidad de la plataforma

Compre el número de parámetros que necesita ahora
Añada más parámetros con la compra de una clave de activación
Incluye el juego completo de filtros de paso de banda reposicionables, filtros no estándar también disponibles para aún mayor flexibilidad

Escaso mantenimiento

Los láseres, ópticas de dirección y cubetas de flujo están todos montados en un tablero aislado de la vibración, manteniendo la alineación óptica
Sistema fluídico a baja presión
El mantenimiento preventivo puede ser realizado por el usuario, sin necesidad de visitas de servicio

Automatización disponible

Cargador de muestras opcional para placas de 96 pocillos
Una API (Interfaz de programación de aplicaciones) permite que software externo controle del instrumento
Para el procesamiento automatizado de muestras y la adquisición de datos, intégrelo con el instrumento Biomek i-Series

Especificaciones del citómetro de flujo CytoFLEX LX

Detection	Fotodiodos
Resolution	<300 nm particles (488 nm side scatter), <80 nm polystyrene particles (405 nm side scatter), rCV 3%
Actuación	<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	C00445

Documentación del citómetro de flujo CytoFLEX LX

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Title	Description
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.
Protection Plan for your Workflows in Flow Cytometry {9E29D7A5-B5EC-470A-A5C1-4EF9BFAE9959}	Maintenance service plan for Beckman flow analyzers.
BeckmanConnect Installation and Activation Instructions {B14306BD-BB46-4B27-BF3E-B11862085BC7}	A step-by-step guide to help you successfully install BeckmanConnect.
Flow Cytometry Training {9E29D7A5-B5EC-470A-A5C1-4EF9BFAE9959}	Real-world training programs to maximize the value of your flow cytometer investment.
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
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 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
Automating Flow Cytometry Brochure {A7DF4F56-8AF9-4BF1-88BE-766AB73FBC6B}	Mitigating sources of variability begins during assay design, continues during analytical method development, and through process monitoring
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
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.
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.
Specifications: CytoFLEX Platform Plate Loaders {A7DF4F56-8AF9-4BF1-88BE-766AB73FBC6B}	Technical Specifications for the Plate Loader options for CytoFLEX platform flow cytometers
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.
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.
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.
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.
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.
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.
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.
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 LX WDM Beam Splitter Technical Note {749D68FB-4893-4B2D-BD6C-C662F0520F64}	Increase the number of UV, Near UV, or Violet excitable dyes that can be detected on the CytoFLEX LX instruments
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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
Manufacturing Processes for Engineered T-Cell Therapy – CAR-T	Brochure presenting the CAR-T cell therapy workflow and associated product portfolio
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.
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.
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.
Use Machine Learning Algorithms to Explore the Potential of Your High Dimensional Flow Cytometry Data Example of a 20–color Panel on CytoFLEX LX {442DF88C-CA7F-4B78-AF75-9D2B985534C0}	Understand how to perform machine learning algorithms like viSNE and FlowSOM to identify phenotypes of populations/subsets present in the 20–color CytoFLEX LX flow cytometry data
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.
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.
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.
BeckmanConnect Security Highlights {749D68FB-4893-4B2D-BD6C-C662F0520F64}	This document highlights the privacy and security features in the BeckmanConnect remote management solution.
a_technical-cytoflex-wdm-beam-splitter_jp {611E05FD-FC41-4E23-9498-DA5662F8D4F9}
フローサイトメトリーによる簡単な17 マーカー、 18カラーのヒト血液フェノタイピング {442DF88C-CA7F-4B78-AF75-9D2B985534C0}	CytoFLEXとDURACloneを用いて18カラーパネルを迅速にデザインし、テストを行う方法を説明します。
【テクニカルノート】フローサイトメーターCytoFLEXを用いた、バイオレットレーザー側方散乱光を利用してナノ粒子を検出する方法 {611E05FD-FC41-4E23-9498-DA5662F8D4F9}	バイオレットレーザー側方散乱光（Violet Side Scatter, VSSC）を用いてナノ粒子を検出する際のフローサイトメーターCytoFLEXの設定方法をご説明します。
【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。