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Sphero™ Blank Calibration Particles, 6.0 - 6.4 µm


Rainbow Particle peak separation based on FL1 fluorescence intensity expressed in relative channel numbers. The Blank Calibration Particles correspond to peak 1 in the Rainbow Calibration Particles depicted in the figure.

Sphero™ Blank Calibration Particles, 6.0 - 6.4 µm
Regulatory Statusの凡例
Becton, Dickinson and Companyの書面による明示的な許諾を得た使用以外での製品の使用は固く禁じられています。
説明
The vial contains a single population of Blank Calibration Particles that are dyed to a single fluorescent intensity. The intensity of this particle corresponds to the dimmest intensity. The intensity of this particle corresponds to the dimmest intensity peak in the Rainbow Calibration Particles, 6.0 - 6.4 µm (Cat. No. 556288). Every Rainbow Particle contains a mixture of fluorophores that are excited at any wavelength from365 - 650 nm. The Rainbow Particles have emission spectra compatible with many common fluorophores used for immunofluorescent staining with flow cytometric analysis.
調製と保管タイトルテキスト
推奨アッセイ手順
This particle mixture (~10x10^6 particles/ml) is useful for routine calibration of flow cytometers. Before use, resuspend the particles by vortexing. Dilution of 3 - 5 drops of particles to 1 ml of sheath fluid will provide an adequate number of particles for flow cytometric analysis.
製品通知
- Since applications vary, each investigator should titrate the reagent to obtain optimal results.
- Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
- Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
- Please refer to http://regdocs.bd.com to access safety data sheets (SDS).
Please refer to Support Documents for Quality Certificates
Global - Refer to manufacturer's instructions for use and related User Manuals and Technical data sheets before using this products as described
Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims. Comparisons are not made against non-BD technologies, unless otherwise noted.
For Research Use Only. Not for use in diagnostic or therapeutic procedures.