L1273
Latex beads, deep blue dyed
0.24 μm mean particle size, aqueous suspension, solids 10 %
Product Name
Latex beads, deep blue dyed, 0.24 μm mean particle size, aqueous suspension, solids 10 %
form
aqueous suspension
composition
solids, 10%
technique(s)
cell based assay: suitable
mean particle size
0.24 μm
application(s)
cell analysis
Quality Level
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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
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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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
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 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
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