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1 T pre-treatment had no effect survival (70%, Alamar Blue).
2 es (ROS) production or the ability to reduce Alamar Blue.
3 rved several drawbacks to the routine use of Alamar Blue.
4           Viability was quantified using the Alamar Blue (AB) assay and by direct morphological exami
5 canning electron microscopy (SEM) as well as alamar blue, acridine orange, and alizarin red assays.
6 rease in fluorescence of the redox indicator Alamar blue and by an increase in lactic acid dehydrogen
7 cyte cell viability (24 h) was assessed with Alamar Blue and Neutral Red assays.
8                 We show here the identity of Alamar Blue as resazurin.
9 iability of cells was tested with a modified Alamar Blue assay (ABA) and scanning electron microscopy
10 ndirect colorimetric methods: the microplate Alamar Blue assay (MABA) and the tetrazolium microplate
11             A colorimetric, microplate-based Alamar Blue assay (MABA) method was used to determine th
12 viability index detected with nondestructive Alamar Blue assay and direct cell count were studied.
13                In vitro assessment using the Alamar blue assay demonstrated a significant reduction (
14                                              Alamar blue assay was performed to check the proliferati
15                                          The Alamar blue assay was used to quantify CGN viability, wh
16 cts of different stimuli were confirmed with alamar blue assay, phase contrast and fluorescence micro
17               Cell viability was measured by alamar blue assay.
18 confocal microscopy and AM cell viability by Alamar Blue assay.
19  similar to those obtained with the standard Alamar Blue assay.
20                                              Alamar blue assays and light microscopy indicate that th
21             Also, the extensive reduction of Alamar Blue by metabolically active cells led to a final
22 68-300mugmL(-1) 24h post-exposure, using the Alamar Blue, CDFA and Neutral Red assays.
23 )-2,5-diphenyl tetrasodium bromide (MTT) and Alamar Blue cell viability assays.
24 P significantly enhanced cell survival (88%, Alamar Blue) compared to control, whereas a-T pre-treatm
25                                              Alamar blue conversion was also compared with [3H]-thymi
26 This study was designed to determine whether Alamar blue could be used to evaluate corneal endothelia
27 etermination (conventional and colorimetric [Alamar Blue] evaluation of growth inhibition) on intra-
28 n accumulation of the fluorescent product of Alamar Blue in the medium which could lead to an overest
29                                              Alamar blue incorporates a proprietary redox indicator t
30 he subdiploid peak) or cell viability assay (alamar blue or 3H-thymidine incorporation).
31 anges after labeling were evaluated using an Alamar Blue reagent, doubling time calculations and quan
32                                              Alamar blue reduction demonstrated endothelial cell viab
33                                              Alamar blue reduction measures endothelial cell viabilit
34 ric assay based on the metabolism of the dye Alamar Blue (resazurin) by live cells.
35                  After 12 hours' incubation, Alamar blue was added to each well and absorbance measur
36 on, although the reduced fluorescent form of Alamar Blue was found in the cytoplasm and of living cel