The phrase "assay to remove" is correct and usable in written English.
It can be used in contexts related to testing or analyzing something in order to eliminate or extract a specific component or substance.
Example: "The laboratory conducted an assay to remove impurities from the sample before further analysis."
Alternatives: "test to eliminate" or "analyze to extract".
The use of the MspI control represents an unusual strength of the HELP assay to remove the potentially confounding effect of copy number variation.
Samples in capped "Low Tube Strips, CLR" (Bio-Rad) were spun down immediately before the assay to remove possible air bubbles.
The accurate RNA concentration was determined via a thermal hydrolysis assay to remove effects of hypochromicity, and the labeling efficiency was calculated as previously described.
To control for the effect of cell viability on the respiratory capacity and aerobic/anaerobic flux analyses, plates were gently washed once with assay buffer immediately after each assay to remove dead cells, before the cell plate was frozen at −80 °C.
After two rounds of limited dilutions, three different individual recombinant clones for each protein were selected to run 2 or 3 times plaque assays to remove parent virus contamination.
Commercially available calf thymus histones (Sigma, Deisenhofen, Germany) were passed through a high affinity endotoxin detoxi-gel (Thermo Fisher Scientific, Waltham, Massachusetts, USA) before use in all stimulation assays to remove potential endotoxin contamination.
Wash the young adult F2 progeny from their plates into a 1.5 ml tube with Assay Buffer (5 mM KPO4 (pH6), 1 mM CaCl2, 1 mM MgSO4), rinse twice more with Assay Buffer to remove bacteria and finally resuspend the worms in Assay Buffer containing 400 mM ethanol.
The liquid in the tubes was replaced twice with Assay buffer to remove bacteria and was then replaced with 400 mM ethanol in Assay buffer.
At the end of the invasion assay, medium from the four wells of the assay was harvested (referred to as end-of-assay CM), centrifuged to remove cell debris, and stored at -80°C until use.
Where EDTA was used in the permeability assay, the assay media was changed to remove EDTA before introducing TCs.
Because GTP is necessarily included in standard G addition assays (and is also present in the cell at concentrations similar to those employed in these assays), the ability to remove pyrophosphate from the base-paired G 1 C73 variant tRNA might also be enhanced in the presence of GTP.
