ライフサイエンスコーパス: latex particle

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1 as not detected in phagolysosomes containing latex particles.

2 ingest both fibronectin and collagen-coated latex particles.

3 ntaining either silica particles or nontoxic latex particles.

4 phagocytosis but not during phagocytosis of latex particles.

5 olayer coverage of the surface by individual latex particles.

6 structures are controlled by the size of the latex particles.

7 .1 were exposed to immune complexes or sized latex particles (0.8 or 3.2 micron in diameter).

8 After 24 hrs, 4-microm-diameter fluorescent latex particles (2 x 10(8)) were infused into the pulmon

9 ted with nanosized (20 nm) carboxyl-modified latex particles (20nCL) and carboxyl-modified CdSe/ZnS q

10 to internalize LPS-coated, but not uncoated, latex particles and because MD2/TLR4-transfected human e

11 C57BL/6 mice were given injections of latex particles and prepared for intravital hepatic micr

12 perimental setup, data analysis, and data on latex particles and yeast cells are presented.

13 ococcus aureus, (b) serum- and IgG-opsonized latex particles, and (c) synthetic soluble and insoluble

14 of monodisperse, highly charged polystyrene latex particles are polymerized within lightly cross-lin

15 Spherical latex particles are uniformly deposited on glass slides

16 n by using the RNA-oligo(dT)30 hybrid on the latex particles as the template and primer, and (ii) PCR

17 solution by oligo(dT)30 covalently linked to latex particles, buffer exchange, and continuous RT and

18 abilized polystyrene latex; remarkably, such latex particles can be readily prepared by aqueous emuls

19 assay requires a flow cytometer, two sets of latex particles coated with pneumococcal polysaccharides

20 Fluorescently labeled core-shell latex particles composed mainly of the thermoresponsive

21 d (1 mum) sulfate-functionalized polystyrene latex particles (designated as 20 nSL and 1 mSL, respect

22 solution environment for a light-scattering, latex-particle-enhanced, homogeneous immunoassay of C-re

23 ynamic volume from calibrations with polymer latex particles in flow-FFF are compared to calibrations

24 onocyte phagocytosis of complement-opsonized latex particles, indicating that B. pertussis infection

25 Microscopic latex particles, modified with a mixed monomolecular fil

26 The magnetic label consists of a latex particle of mean diameter 441+/-6 nm, bearing magn

27 Latex particles of 50-170-nm sizes were covalently coupl

28 ified through film-formation of soft polymer latex particles on the surface of the polymersome, hereb

29 respiratory burst nor phagocytosis of either latex particles or serum-opsonized Staphylococcus aureus

30 Exposure of cells to sized latex particles resulted in a graded, stepwise decrease

31 Using latex particles, silica particles and carbon nanotubes a

32 croscopy was used to prepare digital maps of latex particle trapping patterns (eight per lung).

33 s effect was more pronounced for the smaller latex particles used in this study and highlighted possi

34 In the second method, latex particles were codeposited with the silica by spin

35 Embedded 2.1 microm polystyrene latex particles were displaced 10-100 nm using a near-in

36 C-albumin, Lsr-F, or fluorescent polystyrene latex particles were electrosprayed from aqueous buffer

37 lector interface; namely, on bare Al2O3, the latex particles were rigidly attached as compared to the

38 Macromolecules (40 kDa dextran and 20 nm latex particles) were deposited into the skin using a ph

39 tudied using streptavidin-coated polystyrene latex particles with diameters between 0.944 and 0.090 m

40 onstrated for a mixture of three polystyrene latex particles with different sizes as well as for the

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