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 CellTiter 96^® Non-Radioactive Cell Proliferation Assay (MTT) was used to measure human endometrial cell proliferation. (2085)

Notes: The CellTiter 96^® Non-Radioactive Cell Proliferation Assay was used to measure the inhibitory effects of a monoclonal antibody (DC 101) on VEGF-induced growth of human vascular endothelial cells (HUVEC). (2069)

Notes: The CellTiter 96^® Non-Radioactive Cell Proliferation Assay (MTT) was used to measure the cytotoxicity of SIN-1 on HepG2 cells. SIN-1 is the chemical named in the title that is widely used to generate nitric oxide and superoxide radicles. (2114)

Notes: The CellTiter 96^® Assay (MTT) was used to measure the cytotoxicity of SIN-1 (a chemical which generates nitric oxide and superoxide radicles) on HepG2 cells. (2907)

Notes: This paper compares 3H-thymidine incorporation with the CellTiter 96^® Non-Radioactive Cell Proliferation Assay for measuring lymphocyte proliferation in an assay to detect rabies-specific cell-mediated immunity. The results of both tests were in good agreement; however, the degree of positivity was different and the sensitivity was reported to be greater with the 3H-thymidine incorporation method. (2096)

Notes: The CellTiter 96^® Non-Radioactive Cell Proliferation Assay was used to measure proliferation of human ovarian carcinoma cell line Caov-3. The amount of formazan generated was shown to be directly proportional to the number of living cells by cell counting of trypan blue excluding cells. (2094)

Notes: The CellTiter 96^® Non-Radioactive Cell Proliferation Assay was used to generate growth curves to compare the effects of various steroids on proliferation of primary epithelial cells scraped from human ovaries and subcultured for assay. (2095)

Notes: The authors used the CellTiter 96^® Non-Radioactive Cell Proliferation Assay (MTT) to measure IL-2 stimulated proliferation of CTLL-2 cells. The IL-2 was collected from tissue culture supernatants of cells. (1716)

Notes: The CellTiter 96^® Non-Radioactive Cell Proliferation Assay was used to measure the inhibitory effects of apolipoprotein E or apolipoprotein E dimeric peptide on bovine aortic endothelial (BAE) cells. (1717)

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)

Notes: The CellTiter 96^® Non-Radioactive Cell Proliferation Assay was used to measure viability/cytotoxicity of HuT-78, Jurkat, and Su-4 cells in a study of apoptosis. (0150)

Notes: The CellTiter 96^® Non-Radioactive Cell Proliferation Assay was used to measure proliferation of BaF3 murine lymphoid (pro-B) cells that were engineered to express FGFR-1, FGFR-4 and chimeric receptor containing extracelular domain of FGFR-4 and intracellular domain of FGFR-1. (1719)

Notes: The CellTiter 96^® Assay (MTT) was used to assay cell adhesion on vitronectin or collagen coated plates. (2899)

Notes: The CellTiter 96^® Non-Radioactive Cell Proliferation Assay (MTT) was used to assay cell adhesion on vitronectin or collagen coated plates. (2100)

Notes: The CellTiter 96^® Non-Radioactive Cell Proliferation Assay (MTT) was used to measure cell proliferation. (1732)

Notes: The CellTiter 96^® Non-Radioactive Cell Proliferation Assay (MTT) was used to measure the proliferative effect of follicular fluid (collected from Graafian folicules of 22 ovulatory patients using laparoscopic surgery) on bovine aortic endothelial cells. Intra- and inter-plate coefficients of variation were <9%. (2075)

Notes: CellTiter 96^® Non-Radioactive Cell Proliferation Assay was used to study modulation of endothelial cell proliferation by synthetic peptides. (0227)

Notes: The CellTiter 96^® Non-Radioactive Cell Proliferation Assay (MTT) was used to measure thrombospondin inhibition of bovine aortic endothelial cell proliferation. (1718)

Notes: This CellTiter 96^® Non-Radioactive Cell Proliferation Assay (MTT) was used to assay cell adhesion. A poster with the same title and authors was presented at the 1993 ASCB meeting in New Orleans. (2083)

Notes: The CellTiter 96^® Non-Radioactive Cell Proliferation Assay (MTT) was used to measure inhibition of C-1300 murine neuroblastoma cells. (1730)

Notes: MNB (murine neuroblastoma) cells, containing heat inactivated FBS, were used with the CellTiter 96^® Non-Radioactive Cell Proliferation System. (0087)

Notes: These authors used the CellTiter 96^® Non-Radioactive Cell Proliferation Assay (MTT) to measure toxicity of various agents (including peptides from amyloid beta protein, which accumulate in Alzheimer's disease plaques) on PC12 cells. (1541)

Notes: The CellTiter 96^® Non-Radioactive Cell Proliferation Assay was used to measure proliferation of bovine mammary epithelial cells cultured on plastic or on Matrigel. (2115)