ライフサイエンスコーパス: latex microsphere

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1 colloidal gold nanoparticles and fluorescent latex microspheres.

2 ctive Fab domains of an antibody attached to latex microspheres.

3 ctin ligand, sialyl Lewis(x), was coupled to latex microspheres.

4 44 rats was instilled with rhodamine-labeled latex microspheres.

5 grade transport of red and green fluorescent latex microspheres.

6 ducted with bromide and carboxylate-modified latex microspheres (20, 200, and 500 nm diameter).

7 Latex microspheres and ac cells were visualized as refle

8 d to distinguish between the cell types were latex microspheres and carmine particles.

9 rogradely labeled with rhodamine fluorescent latex microspheres and subsequently intracellularly fill

10 long-circulating liposomes (100-400 nm) and latex microspheres (approximately 800 nm) were determine

11 ripping analysis of gold nanoparticle-loaded latex microspheres as a signal-amplified hybridization t

12 eased phagocytic activity toward fluorescent latex microspheres as well as apoptotic cells, thus unco

13 ptake of colloidal gold particles as well as latex microspheres by HeLa cells.

14 OCT latex microsphere concentration measurements were highly

15 nitors expressing these markers, fluorescent latex microspheres covalently coupled to VC1.1 antibodie

16 Latex microspheres (diameter, 8 microm) were coated with

17 othelium of the vasa recta by perfusion with latex microspheres enabled imaging of the pericytes.

18 apacity of iron-oxide coated sands to remove latex microspheres from water revealed that microsphere

19 s migration, we labeled SVZ cells with inert latex microspheres immediately post-injury.

20 nocytes were labeled and traced by uptake of latex microspheres in skin.

21 by retrograde transport of rhodamine labeled latex microspheres injected into target nuclei.

22 ng stereotaxic injection of rhodamine-filled latex microspheres into the right PBN of seven rats whil

23 oxin B subunit, Fluoro-Gold, and fluorescent latex microspheres) into the thalamus to estimate the nu

24 After 21 days, latex microspheres labeled with fluorescein isothiocyana

25 small injection of either rhodamine-labeled latex microspheres or a red fluorescent emulsion was mad

26 rete injections of red and green fluorescent latex microspheres or injections of wheat germ agglutini

27 eral injections of red and green fluorescent latex microspheres or of wheat germ agglutinin conjugate

28 -HRP or discrete injections of red and green latex microspheres revealed that the caudal and lateral

29 nterior segment OCT system was used to image latex microsphere suspensions in vitro and the AC of uve

30 We found that while there was at least one latex microsphere that could induce CCK secretion and ca

31 of dodecanoic acid and several varieties of latex microsphere (varying in size and surface charge) t

32 e tracing with rhodamine-labeled fluorescent latex microspheres was used to determine whether the hyp

33 l tracer, fast blue dye or rhodamine-labeled latex microspheres, was instilled into the guinea pig tr

34 l retrogradely subplate neurons, fluorescent latex microspheres were injected into primary visual cor

35 Rhodamine latex microspheres were injected into the hypoglossal nu

36 c targets, distinct green or red fluorescent latex microspheres were injected into the PGi and the CN

37 eutrophils assessed by uptake of fluorescent latex microspheres were lower in 24-hr cecal ligation an

38 Iron oxide surface patches on latex microspheres were selectively wetted with liquid l

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