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Standardized cycle threshold (Ct) of each PCR reaction was collected if the dissociation curve indicated no multiple products.
Each mass selective reaction was collected for 50 additive multichannel analyzer scans within 400 to 1,000 atomic mass units (amu).
Each well was filled with 250 mL of resin (3.5% Sephadex G-100, GE Healthcare) and the resin was packed by centrifugation at 3.000 × g for 5'; after addition of 150 mL of resin, the plate was re-centrifuged as above; 10 mL of the PCR template were loaded in each well and the purified reaction was collected by centrifugation as above.
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The products of 10B(n,α)Li nuclear reaction were collected simultaneously giving rise to a single peak.
This raises issues about optimization of the size of a current collector and the area from which the current due to electrochemical reaction is collected [11, 12].
The sodium hydroxide (NaOH) byproduct of the hydrogen producing reaction, is collected within the apparatus for later reprocessing by electrolysis, to recover the Na reactant.
At each temperature, products of the reaction were collected at the point where steady-state conditions were achieved; catalysts were calcined and then re-reduced before proceeding to the next temperature.
Dissociation curves of each reaction were collected to evaluate the quality of the end products.
The sialylated proteins from the reaction were collected on Whatman glass filters.
Photons from the luciferin/luciferase reaction were collected with a CCD camera.
Information regarding any adverse reactions was collected at each follow-up visit.
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