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Merck
모든 사진(1)

주요 문서

56969

Sigma-Aldrich

Micro particles based on polystyrene, dark red

size: 100 μm

동의어(들):

Latex beads from PS, dark red

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모든 사진(1)

About This Item

MDL number:
MFCD06202081
UNSPSC 코드:
12352116
NACRES:
NA.32

Quality Level

100

형태

aqueous suspension

교차

2 % cross-linked

농도

5% (solids)

density

1.05 g/cm3 (density of particles)

저장 온도

2-8°C

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관련 카테고리

애플리케이션

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

개인 보호 장비

Eyeshields, Gloves, type N95 (US)

시험 성적서(COA)

제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.

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문서 라이브러리 방문

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
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
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

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