XTTXML Tunneling Technology
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The cytotoxicity of NSS oil was evaluated using the XTT cell proliferation Kit II according to the method of Zheng et al (2001).
The cytotoxic effect of ISO in HT-29 cells and the concentration of ISO that decreased the cell viability by 50% ([IC.sub.50]) were determined using trypan blue dye exclusion test and XTT assay based on the kit protocol.
2,3-bis(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide (XTT) reduction assay is based on the reduction of XTT tetrazolium formazan by active mitochondria in Candida cells (28).
The cytotoxic effects of gemcitabine and combination of gemcitabine and FA were determined using the XTT assay.
The multiparametric cytotoxicity assay kit used allows the evaluation of the material toxic effects in the same cells through three different parameters: mitochondrial metabolism and respiratory toxicity (XTT); lysosomal integrity and membrane permeability (NR); and cell proliferation and presence of DNA (CVDE).
Viability was measured by XTT assay (a) and the levels of TGF-[beta]1 (b) and [PGE.sub.2] (c) in culture medium were measured by ELISA.
Cerca, "Comparative assessment of antibiotic susceptibility of coagulase-negative staphylococci in biofilm versus planktonic culture as assessed by bacterial enumeration or rapid XTT colorimetry," Journal of Antimicrobial Chemotherapy, vol.
The viability of macrophages was determined using the Cytotoxicity Detection Kit (Roche) based on the measurement of lactate dehydrogenase (LDH) released from damaged cells and the XTT cell proliferation assay (Life Technologies) based on a conversion of the tetrazolium dye XTT to reduce colored form by transplasma membrane electron transport system.
Cell viability was measured with the help of a cell proliferation assay kit (Welgene Inc., Korea), using 2,3-bis-(2-methoxy-4-nitro-5-sulfophenyl)-2H- tetrazolium-5-carboxanilide (XTT).
###homogenized in a###antibacterial agent###observed using XTT