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1 ce nitrotetrazolium blue chloride to produce formazan.
2 te via the formation of an intensely colored formazan.
3 -yl)-2,5-diphenyltetrazolium bromide to blue formazan.
4 t cell proliferation (relative absorbance of formazan: 23.4% +/- 7, 44.6% +/- 7.5, 95.8% +/- 2, 100%,
5 t cell proliferation (relative absorbance of formazan: 23.4% +/- 7, 44.6% +/- 7.5, 95.8% +/- 2, 100%,
6  the reduction of nitroblue tetrazolium into formazan, and hydroxyl radicals (OH( *)) were detected b
7 zol-2-yl)-2,5-diphenyltetrazolium bromide to formazan] and apoptotic index (cytoplasmatic release of
8                                              Formazans (Ar1-NH-N[double bond, length as m-dash]CR3-N[
9 hiazol-2-yl)-2,5-diphenyltetrazolium bromide formazan assay (MTT assay) as a reporter of Abeta-mediat
10 r serum-free culture conditions, with both a formazan assay and [3H]thymidine uptake.
11                    Effects were assayed by a formazan-based colorimetric assay, [(3)H]thymidine incor
12                                  The reduced formazans bind as tridentate ligands and stabilize low-s
13 f cancer cells and produce antiproliferative formazan chelators that interfere with cellular iron hom
14 ation assays (tetrazolium salt conversion to formazan colorimetric assay) were performed beginning 2-
15 ium-5-carboxanilide) to water-soluble orange formazan compounds, the intensity of which can then be d
16 els also modulate the trafficking of the MTT formazan-containing vesicles, suggesting that the traffi
17 (MTT formazan), with the formation of unique formazan crystals on the cell surface.
18      Viability was confirmed by formation of formazan crystals, live-dead staining and caspase-3 acti
19 munohistochemical staining co-localized with formazan deposits resulting from nitro blue tetrazolium
20 limit (10 muM in a coupled assay producing a formazan dye) enables accurate kinetic readouts sensitiv
21                                By means of a formazan dye-based spectrophotometric assay of cell viab
22  reduction to a yellow colored water-soluble formazan dye.
23 -dependent reduction of a tetrazolium to the formazan enables the measurement of nanomole quantities
24 he ability of amyloid peptides to induce MTT formazan exocytosis is closely associated with both thei
25                   Cell growth was assayed by formazan formation and 5-bromo-2'-deoxyuridine (BrdU) in
26 beta-diketiminates, the deprotonated form of formazans, formazanates, have received relatively little
27 ligomers to rapidly induce the exocytosis of formazan formed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diph
28              The dark-blue reaction product (formazan) formed a pattern that was consistent with mito
29 in a greater than 50% decline in the rate of formazan generation in the CA1 pyramidal neuronal layer
30 1) and the conversion of tetrazolium salt to formazan in four SCC cell lines (P = 0.01-0.004).
31 r the intracellular release of metal-binding formazan ligands.
32 zo group and the hydrazone group; thus, each formazan may be present in various forms with different
33                                              Formazan molecules exhibit photochromism because isomeri
34  injury by spectrophotometric measurement of formazan produced from 2,3,5-triphenyltetrazolium chlori
35 -yl)-2,5-diphenyltetrazolium bromide, to its formazan product (MA); DNA synthesis reflected as bromod
36 with a tetrazolium salt (NBT(2+)), forming a formazan product that is visible at 530 nm.
37 rsible and irreversible inhibitors decreased formazan production, whereas conventional enzyme assays
38 es (NAD(H)) was the rate limiting factor for formazan production.
39 ogenase, trypan blue uptake, morphology, and formazan production.
40                 Time course analysis using a formazan salt reduction assay to monitor metabolic activ
41 ular reduction and an N-pyridyl donor on the formazan scaffold led to two effective prochelators.
42 itro blue tetrazolium (NBT) resulted in blue formazan staining of the adventitia, and lucigenin chemi
43 ible, insoluble red product called triphenyl formazan, that can be quantified spectrophotometrically.
44 -2-yl)-2, 5-diphenyltetrazolium bromide (MTT formazan), the formation of which is a widely used cell
45 te, NADPH, reduces tetrazolium violet to its formazan, the color of which reflects the number of livi
46           These results suggest that the MTT formazan-transporting vesicles may be involved in cellul
47  by reduction of the tetrazolium compound to formazan, trypan blue dye exclusion, and clonogenic assa
48 tonation of the NH group, a C6F5-substituted formazan undergoes facile cyclization as a result of int
49 sodium salt] to water-soluble yellow-colored formazan with 1-methoxy-5-methylphenazium methylsulfate
50 nation conditions and the environment of the formazan with a most incisive sensibility of the thermal
51 nation conditions and the environment of the formazan with a most incisive sensibility of the thermal
52 l-2-yl)-2,5-diphenyltetrazolium bromide (MTT formazan), with the formation of unique formazan crystal