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96 well flat black bottomed polystyrene microplates

Manufactured by Corning
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The 96-well flat black-bottomed polystyrene microplates are designed for laboratory applications that require high-performance microplates. These plates feature a flat black bottom surface that enhances optical clarity and reduces background fluorescence or absorbance. The polystyrene construction ensures durability and compatibility with a wide range of laboratory equipment and assays.

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Lab products found in correlation

M1000 pro microplate reader, by Tecan (2 mentions) Celltiter glo 2.0 assay, by Promega (2 mentions)

2 protocols using 96 well flat black bottomed polystyrene microplates

1

Cell Viability Measurement Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
Cell viability was measured every 3 to 6 days over an 18-day time course using the CellTiter-Glo 2.0 assay (Promega) according to the manufacturer’s protocol. Luminescence was measured in 96-well flat black-bottomed polystyrene microplates (Corning) using a M1000 Pro microplate reader (Tecan) with a 1-s integration time.
Mok B.Y., de Moraes M.H., Zeng J., Bosch D.E., Kotrys A.V., Raguram A., Hsu F., Radey M.C., Peterson S.B., Mootha V.K., Mougous J.D, & Liu D.R. (2020). A bacterial cytidine deaminase toxin enables CRISPR-free mitochondrial base editing. Nature, 583(7817), 631-637.
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2

Cell Viability Measurement Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
Cell viability was measured every 3 to 6 days over an 18-day time course using the CellTiter-Glo 2.0 assay (Promega) according to the manufacturer’s protocol. Luminescence was measured in 96-well flat black-bottomed polystyrene microplates (Corning) using a M1000 Pro microplate reader (Tecan) with a 1-s integration time.
Mok B.Y., de Moraes M.H., Zeng J., Bosch D.E., Kotrys A.V., Raguram A., Hsu F., Radey M.C., Peterson S.B., Mootha V.K., Mougous J.D, & Liu D.R. (2020). A bacterial cytidine deaminase toxin enables CRISPR-free mitochondrial base editing. Nature, 583(7817), 631-637.
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