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Data were preprocessed using the standard batch for cross-sectional data as described above (including modulation).
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A standard batch of HeLa cells was used as a positive control and lysis buffer was used as negative control for each run.
(804 g) of kale for a standard batch.
The USP chemical reference standard (Batch No.: F2K133, Cat. No.: 1491300) was used for oxytocin and the European Pharmacopeia Chemical reference standard (Lot No.: 1, Cat. No.: Y000076) was used for the analysis of methylergometrine.
PCR efficiency was determined by obtaining standard curves in triplicate for all primer sets with 4-fold dilutions of a standard batch cDNA.
For both sorption and desorption isotherm experiments, triplicate tests were conducted using the standard batch equilibration method.
In addition, growth rate estimates for individual colonies were generally consistent with population growth rates measured using standard batch culture.
A second standard was used to quantify the exact amount of internal standard in every batch for ongoing assay of experimental variability.
The relative sensitivity and specificity of detection of the HRP-LD5 based assay and the domestic diagnostic kits and Abbott 3.0 kit were above 96%, which is the national standard for batch production quality control.
Two cross-check standards (from a different manufacturer) were included in each batch for standard verification during the run.
It should be noted that the standard fed batch performed here for P. pastoris is rather long at low feed rates, leaving room for optimization.
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