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L1273

Sigma-Aldrich

Latex beads, deep blue dyed

0.24 μm mean particle size, aqueous suspension, solids 10 %

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About This Item

MDL number:
UNSPSC Code:
12162002
NACRES:
NA.56

form

aqueous suspension

Quality Level

composition

solids, 10%

technique(s)

cell based assay: suitable

mean particle size

0.24 μm

application(s)

cell analysis

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Application

Latex beads have been used to study the regulation of primary mesenchyme cell migration in the sea urchin embryo and to gain a better understanding of the role of ecto-NAD+ glycohydrolase, an enzyme predominantly associated with phagocytic cells. Latex beads have also been used to develop a new technique for measuring the plaque-forming cell (PFC) responses to bacterial antigens.

Features and Benefits

Dye incorporated into beads, not surface-linked

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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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C A Ettensohn et al.
Developmental biology, 117(2), 380-391 (1986-10-01)
After their ingression, the primary mesenchyme cells (PMCs) of the sea urchin embryo migrate within the blastocoel, where they eventually become arranged in a characteristic ring-like pattern. To gain information about how the movements of the PMCs are regulated, a
Fan Mao et al.
Scientific reports, 10(1), 6577-6577 (2020-04-22)
Phagosomes are task-force organelles of innate immune systems, and evolutionary diversity and continuity abound in the protein machinery executing this coordinately regulated process. In order to clarify molecular mechanisms underlying phagocytosis, we studied phagocyte response to beads and Vibrio species
C D Muller et al.
Biology of the cell, 68(1), 57-64 (1990-01-01)
In order to gain a better understanding of the role of ecto-NAD+ glycohydrolase, an enzyme predominantly associated with phagocytic cells, we have studied its fate in murine macrophages (splenic, resident peritoneal and Kupffer cells) during phagocytosis of opsonized on mannosylated
O Bagasra et al.
Journal of immunological methods, 49(3), 283-292 (1982-03-26)
A new latex bead technique for measuring the plaque-forming cell (PFC) responses to bacterial antigens is described. This technique has been designed for the study of antigens that cannot be readily coated onto SRBC but may also used for antigens

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