ライフサイエンスコーパス: Alamar Blue

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1 es (ROS) production or the ability to reduce Alamar Blue.

2 rved several drawbacks to the routine use of Alamar Blue.

3 Viability was quantified using the Alamar Blue (AB) assay and by direct morphological exami

4 rease in fluorescence of the redox indicator Alamar blue and by an increase in lactic acid dehydrogen

5 We show here the identity of Alamar Blue as resazurin.

6 iability of cells was tested with a modified Alamar Blue assay (ABA) and scanning electron microscopy

7 ndirect colorimetric methods: the microplate Alamar Blue assay (MABA) and the tetrazolium microplate

8 A colorimetric, microplate-based Alamar Blue assay (MABA) method was used to determine th

9 viability index detected with nondestructive Alamar Blue assay and direct cell count were studied.

10 Alamar blue assay was performed to check the proliferati

11 The Alamar blue assay was used to quantify CGN viability, wh

12 cts of different stimuli were confirmed with alamar blue assay, phase contrast and fluorescence micro

13 Cell viability was measured by alamar blue assay.

14 confocal microscopy and AM cell viability by Alamar Blue assay.

15 similar to those obtained with the standard Alamar Blue assay.

16 Alamar blue assays and light microscopy indicate that th

17 Also, the extensive reduction of Alamar Blue by metabolically active cells led to a final

18 68-300mugmL(-1) 24h post-exposure, using the Alamar Blue, CDFA and Neutral Red assays.

19 )-2,5-diphenyl tetrasodium bromide (MTT) and Alamar Blue cell viability assays.

20 Alamar blue conversion was also compared with [3H]-thymi

21 This study was designed to determine whether Alamar blue could be used to evaluate corneal endothelia

22 etermination (conventional and colorimetric [Alamar Blue] evaluation of growth inhibition) on intra-

23 n accumulation of the fluorescent product of Alamar Blue in the medium which could lead to an overest

24 Alamar blue incorporates a proprietary redox indicator t

25 he subdiploid peak) or cell viability assay (alamar blue or 3H-thymidine incorporation).

26 anges after labeling were evaluated using an Alamar Blue reagent, doubling time calculations and quan

27 Alamar blue reduction demonstrated endothelial cell viab

28 Alamar blue reduction measures endothelial cell viabilit

29 ric assay based on the metabolism of the dye Alamar Blue (resazurin) by live cells.

30 After 12 hours' incubation, Alamar blue was added to each well and absorbance measur

31 on, although the reduced fluorescent form of Alamar Blue was found in the cytoplasm and of living cel

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