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Merck

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號碼:
分類程式碼代碼:
12162002
NACRES:
NA.56

形狀

aqueous suspension

成份

solids, 10%

技術

cell based assay: suitable

平均粒徑

0.24 μm

應用

cell analysis

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應用

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.

特點和優勢

Dye incorporated into beads, not surface-linked

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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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
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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