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56969

Sigma-Aldrich

Micro particles based on polystyrene, dark red

size: 100 μm

Synonym(s):

Latex beads from PS, dark red

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About This Item

MDL number:
UNSPSC Code:
12352116
NACRES:
NA.32

Quality Level

form

aqueous suspension

crosslinking

2 % cross-linked

concentration

5% (solids)

density

1.05 g/cm3 (density of particles)

storage temp.

2-8°C

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Application

Micro particles based on polystyrene, dark red, 100 μm (latex beads) may be used for flow cytometry calibration.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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
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
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

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