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We divided generic products at random in two groups: Batch Group 1 had 10 products that were allocated to use the same batch for in vitro susceptibility testing and in vivo determination of efficacy, and Batch Group 2 had the remaining 10 products allocated to use different batches in vitro than in vivo.
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This underlines the necessity to use the same batches of prick test allergens in multicentre studies.
When SPT is repeated over a longer period it might not be possible to use the same batches over time.
Using the same batch technique, we examined whether PTCs could enhance the aqueous solubility of TCE.
The dual-functional photocatalytic activity of Pt/GO/TiO2 F was maintained during repeated photocatalysis runs using the same batch of catalyst.
Normalised expressions of the AmSesTPS1 and AmGuaiS1 genes to the housekeeping genes were quantified in the 54 samples using the same batch of cDNAs to minimise experimental variation.
Owing to the good mechanical and electrochemical stabilities of the material within the 0.1 0.9 V (vs. SHE) potential window, all the previous CVs were obtained using the same batch of active material.
A calibration curve for ATP concentrations was obtained for each experiment by using the same batch of luciferin-luciferase reagents.
Parallel samples were processed using the same batch of reagents to minimize overall sample-to-sample variations.
Control studies at 1G were performed using the same batch of preincubated spermatozoa and the same incubator but outside the clinostat (Fig. 1a, arrow).
We performed all assays twice using the same batch of kits in each case.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com