Notes: The authors used the CellTiter 96^® AQueous Non-Radioactive Cell Proliferation Assay to determine the number of viable oral mucosal cells in tests to measure the effects of components leached out of three glass ionomer cements used as bases and liners for tooth cavity preparations. (2103)

Notes: The MTS tetrazolium in combination with PMS was used to detect different catabolic activities of bacterial cells grown with different carbon sources. The effect of repression of metabolic pathways was demonstrated in Escherichia coli, Bacillus subtilis, and Pseudomonas stutzeri. Results comparable to the production of [14C]CO₂ from [14C]oleate by E. coli demonstrated the MTS assay is an alternative to the use of radiolabeled compounds. (2102)

Notes: The CellTiter 96^® AQueous Non-Radioactive Cell Proliferation Assay was used to determine that acinar formation on laminin and Matrigel involved cell proliferation of the human submandibular gland cell line (HSG) at a similar rate to cells cultured on plastic. (2124)

Notes: The CellTiter 96^® AQueous System was used to determine that acinar formation on laminin and Matrigel involved cell proliferation of the human submandibular gland cell line (HSG) at a similar rate to cells cultured on plastic. (2912)

Notes: The effect of the phosphorothioate oligodeoxynucleotide S-dC28 on the proliferation of vascular smooth muscle cells in the presence or absence of PDGF was assessed using the CellTiter 96® AQ_ueous Non-Radioactive Cell Proliferation Assay. Additionally, LDH release was monitored using the CytoTox 96® Non-Radioactive Cytotoxicity Assay to determine if S-dC28 was directly cytotoxic to vascular smooth muscle cells. (2549)

Notes: The CellTiter 96^® AQ_ueous Non-Radioactive Cell Proliferation Assay was used to measure the effects of TGF-β, IL-10 and IL-4 on proliferation of human vascular endothelial cells (HUVEC). The authors were able to rule out the possibility that inhibitory effects of TGF-β on TNF-α-induced IL-6 and IL-8 expression was due to inhibition of cell proliferation. (1499)

Notes: The CellTiter 96^® AQ_ueous Non-Radioactive Cell Proliferation Assay was used to determine proliferation of rat aortic smooth muscle cells treated with thrombin or thrombin plus hirudin. (2550)

Notes: CellTiter 96^® AQueous MTS Powder and the CellTiter 96^® AQueous Non-Radioactive Cell Proliferation Assay were used to optimize an assay to test the sensitivity of TR146 human buccal epithelial cells treated with a series of beta-adrenoceptor antagonists. Parameters optimized for their screening assay included: initial cell seeding density, PMS concentration, MTS concentration, and stability of the MTS-formazan. (2090)

Notes: A good general review of the use of tetrazolium compounds including MTS for microculture tetrazolium assays. (2071)

Notes: This paper describes the use of MTS (CellTiter 96^® AQueous Non-Radioactive Cell Proliferation Assay) as an indicator for measuring enzymatic activity of dehydrogenase enzymes. (2111)

Notes: The CellTiter 96^® AQ_ueous Non-Radioactive Cell Proliferation Assay (MTS) was used to measure cell growth in a study to identify Mycobacterium avium contamination of cell cultures. In some cases (normal human fibroblasts), the M. avium contamination did not affect growth while in other cases (T47D) cell growth was slowed. (1497)

Notes: CellTiter 96^® AQueous (MTS) was used to determine viability of TPCK and TLCK treated murine macrophage. (2934)

Notes: CellTiter 96^® AQueous Non-Radioactive Cell Proliferation Assay (MTS) was used to determine viability of TPCK and TLCK treated murine macrophages. (2099)

Notes: The authors used MTS (CellTiter 96^® AQueous Non-Radioactive Cell Proliferation Assay) from Promega and reasoned that low levels of cytokine insufficient to induce proliferation and DNA synthesis may be sufficient to maintain the viability of the bioassay cells in culture. They conclude that the tetrazolium assays are: 1) able to detect 2-16-fold lower cytokine levels than methods based on [3H]-thymidine incorporation; and, 2) achieve higher precision with standard deviations of 1-4% for tetrazolium assays vs. 5-15% for thymidine incorporation. (2116)

Notes: The CellTiter 96® AQueous Non-Radioactive Cell Proliferation Assay was used to establish the differences in growth rates of various clones of human colon cancer cells expressing decorin. (1704)

Notes: The CellTiter 96^® AQueous Non-Radioactive Cell Proliferation Assay was used to examine the effects of gliotoxin treatment on P815 cells. (1720)

Notes: These authors used Promega's CellTiter^® 96 AQueous Non-Radioactive Cell Proliferation Assay in this study. (2119)

Notes: The CellTiter 96^® Non-Radioactive Cell Proliferation Assay (MTT) was used to measure the effects of proCRH on proliferation of CHO-K1 fibroblasts. (1498)

Notes: The CellTiter 96^® AQueous Non-Radioactive Cell Proliferation Assay (MTS) was used to measure the survival of PC-12 cells transfected with the TrkB receptor. The effects of NT-4 and BDNF were compared in a serum-free assay system. The data are expressed as percent survival at 72hr relative to cultures treated with 50ng/ml NGF. (2084)

Notes: The CellTiter 96^® AQ_ueous Non-Radioactive Cell Proliferation Assay was used to measure the number of viable cerebellar granule cells in vitro. Direct counts of cell number were unchanged from day 1 to day 4 but the cells demonstrated an increased ability to reduce MTS reagent. The authors attribute the reduced day 1 metabolism to the effects of in vitro culturing. (1533)

Notes: The CellTiter 96^® AQueous Non-Radioactive Cell Proliferation Assay was used to measure proliferation of airway epithelial cells cultured in air/medium interface stimulation of proliferation of airway epithelial cells obtained by cytology brush. After co-culture, the inserts with airway epithelial cells were transferred to fresh medium and the cell number determined using the CellTiter 96^® AQueous Assay system. (2122)

Notes: The CellTiter 96® AQueous Assay was used to measure proliferation of normal human neonatal foreskin keratinocytes. The MTS assay was compared and shown to be equivalent to the 3H-thymidine uptake method. The absorbance with the MTS method was shown to correlate linearly with cell number up to 20,000/well. (2927)

Notes: The CellTiter 96^® AQueous Non-Radioactive Cell Proliferation Assay was used to measure proliferation of normal human neonatal foreskin keratinocytes. The MTS assay was compared and shown to be equivalent to the 3H-thymidine uptake method. The absorbance with the MTS method was shown to correlate linearly with cell number up to 20,000/well. (2093)

Notes: The CellTiter 96^® AQ_ueous Non-Radioactive Cell Proliferation Assay (MTS) was used to measure the proliferation of the apocomplexan oyster pathogen (a protozoan). The authors used the assay to define selected artificial sea water (high salt) culture system parameters to maximize proliferation, assess selected chemosensitivities, and standardize an assay system for quantitation of cell densities and doubling times. (1503)

Notes: The CellTiter 96^® AQ Assay (MTS) and CytoTox 96^® Assays were compared for measuring toxic effects of cationic liposomes on CaSki (human cervical cancer) cells (2882)