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Molecular Probes™ Cell Sorting Set-up Beads (for green-yellow lasers)

Catalog No. 501121515
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501121515 3 mL
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Catalog No. 501121515 Supplier Molecular Probes™ Supplier No. C16509
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Cell Sorting Set-up Beads (for green-yellow lasers)

Molecular Probes™ Cell Sorting Set-up Beads are reliable standards for flow cytometry sorter instrument setup and calibration. The Cell Sorting Set-up Beads approximate the size, emission wavelength, and intensity of many biological samples, and so can be used to calibrate a flow cytometer’s cell sorting system, including laser source, optics, and stream flow. The beads are optimized for checking cell sorter settings such as drop delay and efficiency (cell loss during sorting).

View information for all flow cytometry calibration and size reference beads.

Cell Sorting Set-up Beads are available for use with UV, blue, green/yellow, and red lasers.These 6.0μm beads for green/yellow lasers are fluorescent-dye infused microspheres that are ideally excited at 570 nm with emission of 575 nm, but may also be exited at 488 nm.

Cell Sorting Set-Up Beads provide:

  • Consistency in production, creating ideal reference standards
  • Confidence through reliable, optimal instrument performance
  • Compatibility—use with any instrument

    Bead Labeling
    As with all of our flow cytometry standard microspheres, the Cell Sorting Set-up Beads are stained internally rather than on the surface. The dyes are therefore insulated from environmental interactions that could cause variable fluorescence output, resulting in excellent signal stability. These 6.0μm fluorescent polystyrene microspheres are supplied as suspensions packaged in dropper vials for convenient dispensation and are available in a choice of four colors (UV, blue, green/yellow, red) to match your laser.

    The dyes used in the manufacture of the Cell Sorting Set-up Beads have been carefully selected to provide emission peaks coincident with cells labeled with commonly used fluorescent dyes. The emission profiles for these standards are intentionally narrow in comparison to cells labeled with a corresponding fluorescent dye. Due to their narrow emission profiles, beads of two different fluorescent colors exhibit minimal spectral overlap, and little or no color compensation is needed when setting up for multicolor experiments.

    Notes:
    These beads are an alternative to PeakFlow™ flow cytometry reference beads.

    For optimal verification of the laser alignment of a cell sorter cytometer, please see our selection of Alignflow™ Flow Cytometry Alignment Beads.
  • Specifications

    Diameter (Metric) 6 μm
    Content And Storage Contains 2 vials Cell Sorting Set-up Beads (1.5 mL per vial). Store in refrigerator (2–8°C) and protect from light.
    Format Suspension
    For Use With (Equipment) Flow Cytometer
    Quantity 3 mL
    Detection Method Fluorescence
    Excitation Wavelength Range 532 or 561⁄575
    Stain Configuration Core
    Shipping Condition Room Temperature
    Product Type Cell Sorting Set-up Beads
    What are Cell Sorting Set-up Beads used for?

    Cell Sorting Set-up Beads (Cat. Nos. C16506, C16507, C16508, and C16509) are reliable standards for flow cytometry cell sorter instrument setup and calibration. The Cell Sorting Set-up Beads approximate the size, emission wavelength, and intensity of many biological samples, and so can be used to calibrate a flow cytometer's cell sorting system, including laser source, optics, and stream flow. The beads are optimized for checking cell sorter settings such as drop delay and efficiency (cell loss during sorting). Cell Sorting Set-up Beads are available for use with UV, blue, green/yellow, and red lasers.

    What is the smallest size that I can detect with the Attune NxT Acoustic Focusing Cytometer?

    The smallest size that you can detect with the Attune NxT Acoustic Focusing Cytometer is 0.5 µm.

    What is the Attune NxT Autosampler?

    The Attune NxT Autosampler, an optional accessory for the Attune NxT Acoustic Focusing Cytometer, enables rapid processing of up to 384 samples. It has broad compatibility with different plate formats, both 96- and 384-well plates. It has an intelligent probe designed to minimize clogging and carryover (<0.5%) and to prevent damage to the instrument. It mixes by aspiration rather than shaking to ensure homogeneity of the sample and maintain cell viability. Is performs automated cleaning as part of the shutdown process of the Attune NxT Cytometer. It provides consistent data regardless of sampling method (tube vs. plate) and collection rate.

    What are the advantages of acoustic-assisted hydrodynamic focusing in flow cytometry?

    -Modular design - Multiple configurations available - field upgradable.
    -Save time - 10X faster speeds with no loss in data quality.
    -Simplified sample prep - No wash, no lyse options, non-clogging fluidics.
    -Enables unique applications - Complex protocols on a broad range of cell types and samples.

    How is the Attune NxT Acoustic Focusing Cytometer different from traditional flow cytometers?

    With the option to be configured with up to 4 lasers and 14 colors for multi-parameter analysis the Attune NxT Acoustic Focusing Cytometer was designed as a modular system to fit most experimental needs and lab budgets. The novel design of the optical path helps ensure precise fixed alignment of four spatially separated lasers onto the sample stream enabling consistency in data over time, superior performance, and superior reliability. The instrument can be configured with up to 4 solid-state lasers (405 nm, 488 nm, 561 nm, and 637 nm) with flat top beam profiles.

    The Attune NxT Flow Cytometer's acoustic focusing uses ultrasonic radiation pressure (> 2 MHz) to transport particles into the center of the sample stream. This pre-focused stream is then injected into the sheath stream, which supplies an additional hydrodynamic pressure to the sample. The combination of these two forces- termed acoustic-assisted hydrodynamic focusing-results in a narrow core stream and uniform laser illumination, regardless of the sample input rate. In traditional cytometers that rely solely on hydrodynamic focusing, the sample core widens to accommodate the increases in flow rate, which results in less uniform laser light illumination.

    What is flow cytometry?

    Cytometry is the measurement of physical or chemical characteristics of cells or particles. Flow cytometry measures these characteristics of cells or particles as they individually pass lasers in a flow cytometer instrument. Flow cytometry is performed on single cells, providing discrete measurements for each cell in the sample. It also provides a statistical distribution of the measured characteristics of the sample.

    A flow cytometer is made up of three subsystems: fluidics, optics, and electronics. Fluidics moves the cells and introduces them for interrogation. Optics generates and collects the light signals. Electronics converts the optical signals to proportional electronic signals for computer analysis.


    For Research Use Only. Not for use in diagnostic procedures.