56969
Micro particles based on polystyrene, dark red
size: 100 μm
Sinonimo/i:
Latex beads from PS, dark red
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About This Item
Prodotti consigliati
Livello qualitativo
Stato
aqueous suspension
Crosslinking
2 % cross-linked
Concentrazione
5% (solids)
Densità
1.05 g/cm3 (density of particles)
Temperatura di conservazione
2-8°C
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Categorie correlate
Applicazioni
Micro particles based on polystyrene, dark red, 100 μm (latex beads) may be used for flow cytometry calibration.
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
Eyeshields, Gloves, type N95 (US)
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I clienti hanno visto anche
Clare L Walker et al.
Cytometry. Part B, Clinical cytometry, 70(3), 154-162 (2006-03-31)
We have previously reported a flow rate calibration method for the determination of absolute CD4(+) T-lymphocyte counts that removes the need for the addition of latex beads to each sample. However, a limitation with this approach is that a calibration
Ethan Schonbrun et al.
Lab on a chip, 12(2), 268-273 (2011-11-01)
The combination of microscopy and flow cytometry enables image based screening of large collections of cells. Despite the proposition more than thirty years ago, adding high resolution wide-field imaging to flow cytometers remains challenging. The velocity of cells in flow
Márta Simon et al.
Water research, 142, 1-9 (2018-05-29)
This paper presents a method for microplastic (MP) mass quantification using a Focal Plane Array-based Fourier Transform Infrared imaging technique. It discusses the issue that particle number is not a conserved base quantity and hence less suited than mass to
K Vorauer-Uhl et al.
Cytometry, 39(2), 166-171 (2000-02-19)
An essential parameter that describes the quality of liposome suspensions is the mean size, respectively the size distribution. Currently several analytical methods including laser light scattering techniques (LLST) are being employed. Here we present an alternative technique using flow cytometry
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