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Hard shell 384 well microplate

Manufactured by Bio-Rad

The Hard-Shell 384-well microplate is a high-density polypropylene microplate designed for various laboratory applications. It features 384 individual wells with a well volume capacity of 80 µL. The plate is compatible with automated liquid handling systems and provides a consistent and uniform well depth and bottom for reliable results.

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2 protocols using hard shell 384 well microplate

1

Dilution Series for qPCR Optimization

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This data set created a dilution series consisting of four 10-fold serial dilution points from 15,000 to 15 molecules, using 10 ng / μl yeast tRNA as a carrier (Roche) and created NTC samples of the same dilution. qPCR was done on a CFX 384 instrument (Bio-Rad). QPCR was performed on a CFX 384 instrument (Bio-Rad) using a 96-well pipetting robot (Tecan Freedom Evo 150). Amplification reactions were performed in 8 μl samples containing 0.4 μl forward and 0.4 μl reverse primer (5 μM each), 0.2 μl nuclease-free water, 4 μl iQ SYBR Green Supermix (Bio-Rad) and 3 μl of standard oligonucleotide. In 384-well plates (Hard-Shell 384-well microplate and Microseal B clear using an adhesive seal (Bio-Rad)), for each of the 4 dilution points, a total of 94 replicate reactions were distributed. In addition, the NTC reaction was repeated 8 times [28 (link)]. This dataset will be referred to as ‘94-replicates-4-dilutions set’. And 44 (4 × 11) amplification curves of the MYCN gene with a diluted concentration of 15, 150, 1500,15,000(11 replicated experiments for each group) were used for subsequent analysis.
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2

Dilution Series for qPCR Optimization

Check if the same lab product or an alternative is used in the 5 most similar protocols
This data set created a dilution series consisting of four 10-fold serial dilution points from 15,000 to 15 molecules, using 10 ng / µl yeast tRNA as a carrier (Roche)
and created NTC samples of the same dilution. qPCR was done on a CFX 384 instrument (Bio-Rad). QPCR was performed on a CFX 384 instrument (Bio-Rad) using a 96-well pipetting robot (Tecan Freedom Evo 150). Amplification reactions were performed in 8µl samples containing) 0.4µl forward and 0.4µl reverse primer (5µM each), 0.2µl nuclease-free water, 4µl iQ SYBR Green Supermix (Bio-Rad) and 3µl of standard oligonucleotide. In 384-well plates (Hard-Shell 384-well microplate and Microseal B clear using an adhesive seal (Bio-Rad)), for each of the 4 dilution points, a total of 94 replicate reactions were distributed. In addition, the NTC reaction was repeated 8 times [9] . This dataset will be referred to as '94replicates-4-dilutions set'. Since our system has 96 reaction channels, we select 44 curve data with concentration gradient from data set for analysis.
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