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The materials required for this process can be seen in ref. 83, and the process is as follows: the reaction mixture is incubated at 23 °C for 10 min, then at 42 °C for 30-60 min.
Once the oligonucleotides are modified and reduced, they are added to nanoparticle suspension and the resulting mixture is incubated overnight followed by the addition of phosphate buffered saline and surfactant such as sodium dodecyl sulphate.
Polyethylene glycol (PEG) with the appropriate amount of LiAc is then added to the mixture of DNA and yeast, and the mixture is incubated at 30°C.
Signals are the result of specific and non-specific binding when a complex probe DNA mixture is incubated on the slide surface containing target DNA.
To isolate exosomes, the reagent is added to a biological sample, and the mixture is incubated at 4°C, followed by precipitation through the standard centrifugation at 10,000 g.
In all assays where H2O2 is quantified by employing HVA-HRP system, the reaction mixture is incubated for different time intervals ranging from 5 min to 1 h [ 4, 6, 18].
Similar(51)
This mixture was incubated for 24 h.
The mixture was incubated at 37°C.
The reaction mixture was incubated at 35°C at 200 rpm.
The mixture was incubated on ice for 20 min.
Such mixture was incubated for 4 h at 22 °C.
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