ライフサイエンスコーパス: fluorescein isothiocyanate dextran

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1 llary density (FCD), plasma was labeled with fluorescein-isothiocyanate-dextran.

2 Diffusion coefficients for fluorescein isothiocyanate-dextrans (10-2000 kDa) determ

3 ng transepithelial resistance and passage to fluorescein isothiocyanate-dextran 4 kDa (FD4).

4 electrical resistance, paracellular flux of fluorescein isothiocyanate-dextran 4 kDa, and mRNA expre

5 ferrin in perinuclear endosomes but not with fluorescein isothiocyanate-dextran, a marker for fluid-p

6 examined by measuring permeability to 4-kDa fluorescein isothiocyanate-dextran and by examining chan

7 e fusion (PL-fusion) was quantified by using fluorescein isothiocyanate-dextran and phase and fluores

8 e demonstrated decreased transferrin uptake, fluorescein isothiocyanate-dextran, and horseradish pero

9 Fluorescein isothiocyanate-dextran angiography, rat anti

10 Microvascular blood flow was assessed by fluorescein isothiocyanate/dextran angiography, with flu

11 HMGB1 levels, ileal mucosal permeability to fluorescein isothiocyanate dextran, bacterial counts in

12 The pH-sensing layer comprised fluorescein isothiocyanate-dextran conjugate immobilized

13 Our results indicate that fluorescein isothiocyanate-dextran enters directly into

14 thylene glycol) (PEG) hydrogel incorporating fluorescein isothiocyanate dextran (FITC-dextran) and te

15 d with water-soluble fluorescent dye (42-kDa fluorescein isothiocyanate dextran (FITC-dextran)), to m

16 orated the fluorescent fluid- phase markers, fluorescein isothiocyanate-dextran (FITC-dex) and Lucife

17 plying a flow cytometric technique to detect fluorescein-isothiocyanate-dextran (FITC-dextran) in aci

18 ithelial electrical resistance and increased fluorescein isothiocyanate-dextran flux (P < .05).

19 th mGluR antagonists significantly decreased fluorescein isothiocyanate-dextran flux across the blood

20 ng transepithelial electrical resistance and fluorescein isothiocyanate-dextran flux.

21 mice (105.9 +/- 13.4 vs 59.6 +/- 10.1 mg/mL fluorescein isothiocyanate-dextran flux; P < .05) and im

22 stance and also reduced paracellular flux of fluorescein isothiocyanate-dextran following a calcium s

23 The SCs of a series of fluorescein isothiocyanate dextrans (four sizes, Mr 16,0

24 sing 376-Da carboxyfluorescein but not 4-kDa fluorescein isothiocyanate-dextran from preloaded liposo

25 ew vessels: high-resolution angiography with fluorescein isothiocyanate-dextran; immunohistochemistry

26 donor cells, previously labeled by injecting fluorescein isothiocyanate-dextran into the zygote, were

27 Mucosal permeability to fluorescein isothiocyanate dextran (molecular weight 400

28 easuring the mucosal-to-serosal clearance of fluorescein isothiocyanate dextran (molecular weight = 4

29 ophores, calcein (molecular weight: 622) and fluorescein isothiocyanate-dextran (molecular weight: 71

30 d that contraction also stimulates uptake of fluorescein isothiocyanate-dextran molecules from the me

31 ns correlated with increased permeability to fluorescein isothiocyanate-dextran molecules.

32 l endothelial cells in culture to a group of fluorescein isothiocyanate dextrans of different molecul

33 Paracellular permeability was assessed by fluorescein isothiocyanate-dextran passage in both lines

34 s assessed by apical-to-basal transport of a fluorescein isothiocyanate dextran probe (FD-4).

35 ty at 12 and 24 hours (as assessed by 70-kDa fluorescein isothiocyanate-dextran transmucosal flux); i

36 Intestinal permeability was investigated by fluorescein isothiocyanate-dextran uptake assay, quantit

37 theter was placed and, 30 mins before death, fluorescein isothiocyanate Dextran was injected.

38 This fluorescence appeared more intense when fluorescein isothiocyanate-dextran was used.

39 fined as the extent of vascular filling with fluorescein isothiocyanate/dextran) was significantly de

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