Sentence examples for mixture of final from inspiring English sources

Standardised mean differences were selected to make comparisons across studies that used different tools to measure the same outcome, 22 or reported a mixture of final value scores and change from baseline scores.

For comparisons across trials that reported different measurement tools for the same outcome 19 or a mixture of final value scores and change from baseline scores, standardised mean differences were selected.

The mixture (25 μl of final volume) used for monitoring adenylyl sulfate ammonia adenylyltransferase activity during purification of the lupin enzyme contained 500 mM NH4HCO3, 1 mM SO4-pA or 1 mM F-pA and the analysed fraction.

This lipid substrate (6 μM PI5P) and recombinant lipid kinase were added to the reaction mixture (200 μl of final volume) with 10 μCi [γ-P]ATP and incubated at 30°C for 10 60 min.

Hydroquinone dioxygenase was assayed spectrophotometrically by monitoring the change in absorbance between 230 and 330 nm in a reaction mixture of 1 ml final volume containing 0.1 mM hydroquinone, TD buffer, and cell-free extract (0.1 mg of protein).

Nuclear extracts for topoisomerase assays and Western blot analysis were prepared as described before [ 19, 20], except that a mixture of protease inhibitors (final concentrations: 2 μg/ml aprotinin, 2 μg/ml leupeptin, 1 μg/ml pepstatin A, 2 μg/ml antipain, 100 μg/ml PMSF) was added to the extraction buffers.

A fraction of the homogenate was centrifuged at 700× g for 15 min at 4°C and the resulting supernatant was mixed with sucrose (final concentration 250 mM) and Percoll (15% of final mixture).

The volume of final mixture was adjusted to 500 μl.

At the end of incubation, 200  μL of final mixture was transferred in an optically clear 96-well flat bottom microtiter plate.

The optimized IS481 MB assay was performed in a 20 μl of reaction mixture with final concentrations of 1X LightCycler™ FastStart DNA master hybridization probes mix, 3 mM MgCl2, 0.1 μM of each primer, 0.3 μM of the IS481 molecular beacon and 5 μl of extracted template DNA.

The optimized IS1001 MB assay was performed in 20 μl of reaction mixture with final concentrations of 1X LightCycler™ FastStart DNA master hybridization probes mix, 4.5 mM MgCl2, 0.2 μM of each primer, 0.4 μM of the IS1001 molecular beacon and 5 μl of extracted template DNA.