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Infinite 200 pro nanoquant multimode microplate reader

Manufactured by Tecan
Sourced in Switzerland

The Infinite® 200 PRO NanoQuant Multimode Microplate Reader is a laboratory instrument designed for precise and accurate measurements of sample concentrations in microplates. It is capable of detecting and quantifying various analytes, including proteins, nucleic acids, and small molecules.

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4 protocols using infinite 200 pro nanoquant multimode microplate reader

1

Quantification of Citrullinated Histone H3

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Citrullinated histone H3 (H3Cit) was quantified with a slight modification of the ELISA previously described by Thalin et al. (19 (link)) by using Cell Death detection kit without streptavidin-precoated wells. The optical densities (ODs) were measured at a wavelength of 450 nm with a reference correction wavelength at 620 nm using a microplate photometer (Infinite® 200 PRO NanoQuant Multimode Microplate Reader, Tecan).
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2

Quantifying Circulating Cell-free DNA

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The Quant-it™ PicoGreen assay kit (Invitrogen, San Diego, CA, USA) was used to quantify circulating cell-free double-strand DNA according to manufacturer’s instructions. Fluorescence intensity was measured using a microplate photometer (Infinite® 200 PRO NanoQuant Multimode Microplate Reader, Tecan; 480 nm excitation wavelength/523 nm emission wavelength).
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3

MTT Assay for Cell Viability

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Cell viability was estimated using MTT assay. Briefly, cells were seeded into 96-well plates at a density of 1 × 104 cells/mL. On the following day, cells were incubated with drugs diluted in cell culture medium for an appropriate time. Cells were then incubated with MTT (0.5 mg/mL) for additional 3 h, and the medium was replaced with DMSO (100 μL/well) to dissolve the formazan crystals. The absorbance at 570 nm was measured using Infinite® 200 PRO NanoQuant Multimode Microplate Reader (Tecan Trading AG, Switzerland). Assays were repeated at least three times in quintuplicate.
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4

MTT Assay for Cell Viability

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MTT assay was used to detect cell viability. The cells were inoculated in 96-well plates at a density of 1 × 104 cells/mL. On the second day, after the cells were completely adherent, the drug was diluted to a suitable concentration using the medium, and then it was used to culture the cells for a specified time. After that, 20 uL MTT (0.5 mg/mL) was added to each well, and the culture was continued for 3 h. Finally, the medium was discarded and DMSO (100 μL/well) was added to dissolve the formazan crystal. The absorbance at 570 nm was measured using Infinite® 200 PRO Nano Quant Multimode Microplate Reader (Tecan Trading AG, Männedorf, Switzerland). Each group had 5 replicates. The detection was repeated at least 3 times.
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