Notes: The ability of human bombesin receptor subtype 3 (hBRS-3) to stimulate cell proliferation in the human lung cancer cell line, NCI-N417 was assessed using the CellTiter 96® AQ_ueous Non-Radioactive Cell Proliferation Assay. (2532)

Notes: The effect of anti-SHP-2 antibody electroporation on ANG II-induced vascular smooth muscle cell proliferation was determined using the CellTiter 96^® AQ_ueous Non-Radioactive Cell Proliferation Assay. (2552)

Notes: Rat aortic smooth muscle cells  were cultured in 96-well plates and growth arrested. The quiescent cells were treated with a variety of concentrations of all-trans retinoic acid with our without endothelin. Cell proliferation of the cells was assessed using the CellTiter 96^® AQ_ueous Non-Radioactive Cell Proliferation Assay. (2551)

Notes: Schwann cells were incubated for 6 days in the absence or presence of heregulin peptide, either with or without forskolin, and cell proliferation was measured using the CellTiter 96^® AQ_ueous Non-Radioactive Cell Proliferation Assay. (2542)

Notes: Chemotaxis in THP-1 human monocytic cells expressing the chemokine receptor 2 was examined using a 96-well chemotaxis chamber. Cell migration was assessed by using the CellTiter 96^® AQ_ueous Non-Radioactive Assay. (2544)

Notes: The CellTiter 96^® AQ_ueous Cell Proliferation Assay (MTS/PMS) was used to monitor cell viability of the Hs27 human diploid fibroblast cell line following treatment with ceramide. (1507)

Notes: The CellTiter 96^® AQ_ueous Non-Radioactive Cell Proliferation Assay was used to monitor the proliferative response of human umbilical vein endothelial cells to VEGF-C. RT-PCR was performed in the presence of RNasin^® Ribonuclease Inhibitor. (0146)

Notes: The CellTiter 96^® AQ_ueous Non-Radioactive Cell Proliferation Assay (MTS/PMS) was used to assess the viability of rat embryonic hippocampal neurons 72 hours after treatment with apoE and CNTF. (1191)

Notes: The CellTiter 96^® AQ_ueous Non-Radioactive Cell Proliferation Assay was used to quantify the cytotoxicity of sodium arsenite in TRL 1215 cells. (2547)

Notes: The MTS-based CellTiter 96® AQueous Non-Radioactive Cell Proliferation Assay was used to measure the effects of soluble IL-5Ra or anti-IL-5 mAb (TRFK-5) on survival of human eosinophils. (2077)

Notes: The CellTiter 96^® AQ_ueous Assay (MTS Reagent) was used to measure the cytotoxic activity of wildtype and mutant soluble Fas ligand (sFasL) on murine B lymphoma A20 cells and human T lymphoblastoma Jurkat cells. (1706)

Notes: The CellTiter 96^® AQueous Assay (MTS reagent) was used to measure the cytotoxic activity of wild type and mutant soluble Fas ligand (sFasL) on murine B lymphoma A20 cells and human T lymphoblastoma Jurkatt cells. (2861)

Notes: The CellTiter 96^® AQ_ueous Cell Proliferation Assay (MTS/PMS) was used to measure the IC₅₀ for anti-MpL ligand. Murine 32D cells that were transfected with the human MpL receptor. (1251)

Notes: Various growth factors were labeled with digoxigenin or biotin. The authors tested the ability of the labeled growth factors to stimulate proliferation of the human megakaryoblastic leukemia cell line, M-07e; the human erythroleukemia cell line, TF1; and the human plasmacytoma cell line T1165. Cell proliferation was assayed using the CellTiter 96^® AQ_ueous Non-Radioactive Cell Proliferation Assay. (2531)

Notes: Both sense and antisense bcl-2 and cytochrome P4502E1 cDNAs were stably expressed in a HepG2 derived cell line using the pCI-Neo Mammalian Expression Vector. Cytotoxicity of arachidonic acid to transfected and control cells was assessed using the CellTiter 96^® Non-Radioactive Cell Proliferation Assay. (1328)

Notes: Fragments of the pp65 protein cDNA were subcloned into a modified pCI-neo Mammalian Expression Vector containing an enterokinase cleavage site and 6XHis tag. These fusion vectors were co-transfected into COS cells with an HLA A*0201 gene-expressing pCI-Neo Vector construct. The transfected cells were assayed for TNFα production. TNFalpha was quantified by its cytotoxicity to WEHI-164 cells using the CellTiter 96^® AQ_ueous Non-Radioactive Cell Proliferation Assay (MTS/PMS). (1231)

Notes: CellTiter96® AQ_ueous Non-Radioactive Cell Proliferation Assay was used to measure proliferative responses in various cancer cell lines: HeLa (cervical carcinoma); Saos-2 (osteosarcoma); ht-1080 (Fibrosarcoma); M2 (melanoma); and HCT116 (colon carcinoma). (0439)

Notes: The CellTiter 96® AQueous Non-Radioactive Cell Proliferation Assay was used to measure suppression of the number of proliferating cells expressing or growing in the presence of decorin. Various cell types were used including Saos-2 osteosarcoma, HL-60 promyelocytic, HT-1080 fibrosarcoma, HeLa cervical carcinoma, M2 mouse melanoma, and HCT116 colon carcinoma cells. (1703)

Notes: The CellTiter 96^® AQ_ueous (MTS/PMS) Non-Radioactive Cell Proliferation Assay was used to measure HCMV-associated suppression of oxidative activity of peripheral blood mononuclear cells (PBMC) from healthy human donors. (2078)

Notes: In this paper, the CellTiter^® 96 AQ_ueous Non-Radioactive Cell Proliferation Assay was used to study TNF-induced toxicity and rescue by TGF-Beta1 of  LNCap, L929, and Mv 1 Lu cells. (1361)

Notes: The MTS-based CellTiter 96^® AQ_ueous Non-Radioactive Cell Proliferation Assay was used to measure viability of rat glial cells treated with antisense oligodeoxynucleotide. (1539)

Notes: This paper reports the characterization of the apoptosis inhibitor protein, FLIP. FLIP-transfected Jurkat and Raji clones were assayed for sensitivity to FasL, sTRAIL, and staurosporine using the CellTiter 96^® AQ_ueous Non-Radioactive Assay. Staurosporine-induced apoptosis was not inhibited by FLIPs. (2517)

Notes: The MTS-based CellTiter 96^® AQueous System was used to assess the proliferative response of T-cells (20,000 per well) to mitomycin C-treated splenocyte antigen-presenting cells (10,000 per well) and Concanavalin A. T-cells isolated from the lung and spleen of normal mice were compared to transgenic mice expressing IL-4 constitutively in lung tissue. The lung T-cells from the transgenic mice proliferated in response to the antigen-presenting cells. (2989)

Notes: The CellTiter^® 96 AQ_ueous Non-Radioactive Cell Proliferation Assay (MTS/PMS) was used to measure cell MDCK cell survival during an anoikis assay. (0938)

Notes: The CellTiter 96^® AQueous (MTS/PMS) Non-Radioactive Cell Proliferation Assay was used to measure dose-response Z-VAD-FMK inhibition of apoptosis of MDCK cells by measuring cell survival. The effect of treatment with Z-VAD-FMK on cell survival in response to detachment (suspension for 12 hours, then re-platting) was measured. (2098)