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After pretreatment, the cellulose rich water insoluble components were washed, filtered and refrigerated for long-term storage.
The components were washed and mixed at a ratio 3 5 5, jars were filled with the mixture and sterilised at 160°C for 24 h.
Analytes were preconcentrated using high-performance liquid chromatography on a guard column, and the remaining urine components were washed off, using 10% methanol in 0.1% formic acid, into a waste container.
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When a biological sample is applied to the coated antibody, enzyme is captured and other matrix components are washed away.
Unbound serum components are washed off and bound antibodies are detected after incubations with anti-human IgG conjugated to HRP Horse Radish Peroxidasee) and specific enzyme substrate (TMB) as per manufacturer's protocol.
For localization of microtubules and centriole/centrosomal components, testes were washed for 15 min in PBS and incubated for 1 h in PBS containing 0.1% bovine serum albumin (PBS BSA) to block non-specific staining.
These products were then captured by streptavidin-coated magnetic beads, while the unextended primers and other components in the reaction were washed away.
Inorganic components such as calcium and magnesium were washed out and partially redistributed over the fiber surfaces.
The disaggregated residues were washed through a 0.25-mm mesh screen to separate large components from microscopic components including starch.
Then the cells were washed twice with ice-cold PBS to remove other blood components and the gradient medium.
The evacuolated protoplasts were washed and then disrupted by nitrogen decompression to protect labile cell components from oxidation [ 18].
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CEO of Professional Science Editing for Scientists @ prosciediting.com