Notes: Various synthetic dinitroanilines were synthesized and evaluated for their potential to inhibit the infection of MDCK Madin-Darby canine kidney cells by Cryptosporidium parvum. The toxic effects of the synthesized dinitroanilines on the MDCK cells was evaluated with the CellTiter 96^® Non-Radioactive Cell Proliferation Assay (MTT). (1437)

Notes: The MTT-based CellTiter 96^® Non-Radioactive Cell Proliferation Assay was used to assess the survival of primary sympathetic neurons from the rat superior cervical ganglion. The effects of NT-4, NGF, BDNF, interaction with the p75 neurotropin receptor were investigated. (1540)

Notes: The CellTiter 96® Non-Radioactive Cell Proliferation Assay (MTT) was used to monitor the toxic effects of uninfected human foreskin fibroblasts after exposure to the naphthoquinones being tested for anti-toxoplasma activities. (0933)

Notes: The affect of the RGD peptidomimetic SC56631 on the ability of human K562 erythroleukemia cells and human embryonic kidney 293 cells to adhere to fibronectin was assessed. Cells were preincubated with the test compound and then plated in 96-well plates coated with fibronectin. Plates were washed, and attached cells were quantitated using the CellTiter 96^® Non-Radioactive Cell Proliferation Assay. (2518)

Notes: The inhibition of proliferation of Saos-2 human osteosarcoma cells was monitored with the CellTiter 96^® Non-Radioactive Cell Proliferation Assay (MTT). (0161)

Notes: The CellTiter 96^® Non-Radioactive Cell Proliferation Assay (MTT version) was used to determine relative cell number in growth inhibition assays using human osteosarcoma cells and murine embryonic fibroblasts lacking endogenous p53 expression. Saos2 cells and (10)1 fibroblast clones were transfected to contain inducible p53as or p53 and demonstrated to be growth inhibited upon expression of those genes. (1727)

Notes: The CellTiter 96^® Non-Radioactive Cell Proliferation Assay was used to measure proliferation of murine MC-38 colon adenocarcinoma cells treated with supernatants from CD4+ T cells activated with anti-CD3 and IL-2. (1705)

Notes: The CellTiter 96® Non-Radioactive Cell Proliferation Assay was used to monitor the in vitro proliferation of SKOV3.ipl human ovarian tumor cells. (1391)

Notes: The CellTiter 96^® Non-Radioactive Cell Proliferation Assay was used to determine if hyaluronic acid (HA) stimulates growth of SKOV3.ipl human ovarian carcinoma cells. (1496)

Notes: The MTT-based CellTiter^® 96 Non-Radioactive Cell Proliferation Assay was used to investigate cell density and cell viability in response to different concentrations of dehydroepiandrosterone, xythiamine, or combinations on MIA PaCa-2 pancreatic carcinoma cells. (1495)

Notes: The Access RT-PCR System was used to demonstrate expression of the transfected cDNAs in cells. The CellTiter 96^® Non-Radioactive Cell Proliferation Assay (MTT) was used to monitor cell survival after diphtheria toxin exposure. (0698)

Notes: The Altered Sites^® II in vitro Mutagenesis System was used to generate a 237 base deletion in the N-terminal portion of the interleukin-3 receptor alpha chain, and to insert a premature stop codon to produce a C-terminal truncation. Mutations were created using the single stranded DNA protocol. Mutants were expressed in FDC-P1 cells and assayed for proliferation in response to rhIL-3 using the CellTiter 96^®  Non-Radioactive Cell Proliferation Assay (MTT). (1463)

Notes: The PolyATtract^® System 1000 was used to isolate polyA+ RNA directly from newborn mouse brains. The RNA was used in RT-PCR for detection of specific TrkB variants. Taq DNA Polymerase and the pGEM^®-T Vector System were used to produce and subclone novel TrkB variants that differ in the extracellular domain. The CellTiter 96^® Non-Radioactive Cell Proliferation Assay was performed on NIH 3T3 cells transfected with the TrkB receptors and challenged with BDNF, NT3 and NT4/5. (0615)

Notes: The CellTiter 96^® System was used to determine the antiproliferative activity of 4HPR on various cell lines including T47D, MCF-7, Hs578T, Calu-6, H661, HeLa, and CV-1. (2880)

Notes: The MTT-based CellTiter 96^® System was used to measure survival of rat primary sympathetic neurons in response to infection with varying titers of adenovirus or HSV-1. TUNEL staining using Promega's TdT also is shown. (2950)

Notes: The CellTiter 96^® Non-Radioactive Cell Proliferation Assay was used to measure the effects of combinations of βFGF and steroids (estradiol or progesterone) on proliferation of Balb/3T3 fibroblasts and bovine aortic endothelial cells (1502)

Notes: The MTT-based CellTiter 96^® Non-Radioactive Cell Proliferation Assay was used to measure proliferation in primary cultures of rat uterine stromal cells stimulated by combinations of steroid hormones and bFGF in serum-free medium. (2082)

Notes: The authors compared MTT (CellTiter 96^® Non-Radioactive Cell Proliferation Assay) and MTS (CellTiter 96^® AQueous Non-Radioactive Cell Proliferation Assay) tetrazolium salts and report that DT-diaphorase inhibitors abolish MTS but not MTT formazan production. The authors conclude that MTT and MTS/menadione resulted in formazan production via a different electron transfer pathway. (2117)

Notes: A CellTiter 96® Non-Radioactive Cell Proliferation Assay was used to determine that dexamethasone treatment did not affect IGF-I induced proliferation of Swiss 3T3 cells. The authors report the use of MTS; however, they describe the use of the Solubilization Solution and recording absorbance at 570nm which implies they were using the MTT-based assay. (2121)

Notes: The MTT-based CellTiter 96^® Non-Radioactive Cell Proliferation Assay was used to measure interferon-enhanced antiproliferative activity of retinoids on MCF-7 breast cancer cells. (2113)

Notes: The CellTiter 96^® Non-Radioactive Cell Proliferation Assay was used to measure growth of NIH 3T3 and the HC11 clone of the mouse mammary COMMA-1D cells. Cells exposed to 20 J/m² UVC in the presence of 50µM suramin were growth inhibited compared to controls without suramin treatment. (2087)

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

Notes: The CellTiter 96® Non-Radioactive Cell Proliferation Assay was used to measure growth effects of N-nitrosonornicotine on hamster oral epithelial cells cultured in keratinocyte serum-free medium. (1708)

Notes: The authors used the CellTiter 96^® Non-Radioactive Cell Proliferation Assay (MTT) and Anti-β-Galactosidase mAb in a TF-1 cell line. (1034)

Notes: In this paper, the CellTiter 96^® Non-Radioactive Cell Proliferation Assay was used to assess cell viability. (1518)