Guava easyCyte 8HT Base System from EMD Millipore

Description

The Guava easyCyte 8HT System provides absolute cell counts and offers other high-demand features, such as eight parameters (6 fluorescent colors, 2 light scatter) and has a blue laser and red laser for access to commonly used fluorescent dyes.

It also offers a built-in 96-well autosampler, which allows researchers to obtain even more data while performing more complex biological studies such as white blood cell phenotyping, cell signaling, cytokine production, activation marker analysis, and multiplex compound screening. Monitoring the interplay of up to eight different biological mechanisms simultaneously improves the efficiency of experimental outputs. Not only does this shorten the number of iterations for any one experiment, it also comes that much closer to mimicking the complex biological responses within the body.

The Guava easyCyte 8HT System runs all Guava Assays and uses Guava InCyte software for data acquisition and analysis. Guava InCyte offers drag and drop gating, pre and post acquisition compensation, heat map display and IC50/EC50 curve generation.

  • Detailed Specifications
  • ItemGuava easyCyte 8HT Base System
  • CompanyEMD Millipore
  • PricePricing InfoGet QuoteGet Quote for this Product
  • Catalog Number0500-4008
  • QuantityEach
  • ApplicationsStem Cell Research
    Signaling
    QC and Maintenance
    Chemokine Analysis
    Cell Tracking
  • Detection5 Colors
  • Absorbance / Excitation488 nm
    640 nm
  • Sample Type96 Well Plates
    1.2 or 1.5 mL Tubes
  • Volume125 µL
  • Throughput12 to 60 µL/min
EMD Millipore
EMD Millipore
EMD Millipore is the Life Science division of Merck KGaA of Darmstadt, Germany Millipore Corporation 290 Concord Road
Billerica, Massachusetts 1821
United States
Phone: (800)-645-5476
(800)-645-5439
Company Profile
Website: www.emdmillipore.com/

  • Cell Sorting Based on RNA Detection in Living Cells Using SmartFlare™ RNA Detection Reagents

    Cell sorting enables the isolation of highly pure cell subpopulations, increasing the statistical significance of observed relationships between gene expression and phenotype, especially for rare events. Live cell sorting has traditionally been accomplished by detecting the presence of unique cell surface proteins, which have been identified through the use of fluorescently labeled antibodies. However, live cells cannot be sorted based on endogenous intracellular protein markers, because cells have to be fixed and permeabilized for antibody staining. Sometimes cells can be sorted on the basis of transfected reporter constructs; however, this treatment also compromises cell integrity and may perturb cellular pathways, confounding downstream analyses. Read More

  • Rapid Counting of Somatic Cells in Dairy Milk Using the Scepter™ 2.0 Cell Counter, Following Spin-Wash Sample Preparation

    Mastitis is an inflammatory change in the mammary gland characterized by pathological changes in mammary tissue. This potentially fatal infection is the most common and most costly disease facing the United States dairy industry1. Read More

  • Immuno-monitoring using the Scepter™ 2.0 Cell Counter and Software Pro

    Biological samples such as primary isolates or cultured cells are often heterogeneous mixtures of cells that differ by type and/or function. Such differences in cellular attributes are most commonly determined by multicolor fluorescent antibody detection of cell typespecific surface marker(s) using flow cytometry. Notably, in addition to variations in protein expression, many cell types and physiological states are also uniquely distinguishable on the basis of size alone. The ability to identify population subsets on the basis of phenotypic differences and further determine their relative frequencies (and concentrations) is critical to many aspects of research. Read More