Cell viability assays are widely used to assess the effect chemotherapeutic drugs and other agents on cell lines and have shown promise for the prediction of tumour chemosensitivity. In this study we have compared two viability assays using Daudi and CCRF-CEM cell lines over a range of 1500-100,000 cells/well of a microplate. The ATP assay was able to detect the lower limit of 1563 cells/well with luminescence values at least 100 x background readings, while the MTT assay could not detect less than 25,000 cells/well above background readings. The ATP assay also showed better reproducibility and sensitivity when cells were grown in microtitre plates over several days, and is particularly useful for the measurement of viability with low cell ...
Objectives. There is no basis for choosing one chemotherapy over another in platinum-resistant epith...
Many cell culture experiments involve large number of samples to be analyzed, either for monitoring ...
Serum-free culturemethods for patient-derived primary glioma cultures, selecting for glioma stem-lik...
Cell viability assays are widely used to assess the effect chemotherapeutic drugs and other agents o...
Cell viability assays are widely used to assess the effect chemotherapeutic drugs and other agents o...
Cell viability assays are widely used to assess the effect chemotherapeutic drugs and other agents o...
Cell viability assays are widely used to assess the effect chemotherapeutic drugs and other agents o...
Cell viability assays are widely used to assess the effect chemotherapeutic drugs and other agents o...
Cell viability assays are widely used to assess the effect chemotherapeutic drugs and other agents o...
Cell viability assays are widely used to assess the effect chemotherapeutic drugs and other agents o...
Cell viability assays are widely used to assess the effect chemotherapeutic drugs and other agents o...
Cell viability is defined as the number of healthy cells in a sample and proliferation of cells is a...
Cell viability is defined as the number of healthy cells in a sample and proliferation of cells is a...
Background. Intrinsic radiosensitivity using the clonogenic assay and the cell surviving fraction at...
Background and Purpose: Measuring the proliferation and survival of cells is very important when stu...
Objectives. There is no basis for choosing one chemotherapy over another in platinum-resistant epith...
Many cell culture experiments involve large number of samples to be analyzed, either for monitoring ...
Serum-free culturemethods for patient-derived primary glioma cultures, selecting for glioma stem-lik...
Cell viability assays are widely used to assess the effect chemotherapeutic drugs and other agents o...
Cell viability assays are widely used to assess the effect chemotherapeutic drugs and other agents o...
Cell viability assays are widely used to assess the effect chemotherapeutic drugs and other agents o...
Cell viability assays are widely used to assess the effect chemotherapeutic drugs and other agents o...
Cell viability assays are widely used to assess the effect chemotherapeutic drugs and other agents o...
Cell viability assays are widely used to assess the effect chemotherapeutic drugs and other agents o...
Cell viability assays are widely used to assess the effect chemotherapeutic drugs and other agents o...
Cell viability assays are widely used to assess the effect chemotherapeutic drugs and other agents o...
Cell viability is defined as the number of healthy cells in a sample and proliferation of cells is a...
Cell viability is defined as the number of healthy cells in a sample and proliferation of cells is a...
Background. Intrinsic radiosensitivity using the clonogenic assay and the cell surviving fraction at...
Background and Purpose: Measuring the proliferation and survival of cells is very important when stu...
Objectives. There is no basis for choosing one chemotherapy over another in platinum-resistant epith...
Many cell culture experiments involve large number of samples to be analyzed, either for monitoring ...
Serum-free culturemethods for patient-derived primary glioma cultures, selecting for glioma stem-lik...