Sentence examples for test buffer from inspiring English sources

In order to quickly test buffer systems if the evaporation of electrophoresis solutions is acceptable, an alternative experimental design without doing CE experiments had to be found.

As the sensitivity of the blood assay might be improved in the same way, this possibility has been examined under both laboratory and field conditions, by adding EDTA to the test buffer or, as an anticoagulant, to the blood samples.

The test buffer (110 μL/well) was applied onto the micro titer plates and the enzyme lysates (40 μL) were added.

Test buffer for 8 plates consisted of acetonitrile (4.4 mL), substrate 1 (121 μL, final concentration in the reactions 10 mM) and potassium phosphate buffer (100 mM, pH 7.4, 83.6 mL).

For pH stability studies, the enzyme samples were incubated in different test buffer solutions with varying pH (pH 2.0, pH 5.0, pH 7.0, pH 9.0, and pH 11.0) for 30 to 60 min at 60 °C, and then the residual enzyme activities were measured in sodium citrate buffer (50 mM, pH 5.0).

The acidic and alkaline partner solutions (each having 10 mM lithium ion) were mixed at room temperature to achieve the desired pH of each test buffer.

Conductivity measurements are generally applicable to quickly test buffers that contain organic solvents.

The enzyme activities were found to be nearly similar in all test buffers with varying pH.

The solubility of the compounds was estimated via the turbidimetric method using standard test buffers (pH 2.0 and pH 6.5) as previously described [23].

Sensitivity and specificity were entered as 95.4% and 99.9% respectively [28], [29] as an imperfect test, Buffered antigen plate agglutination test (BPAT), was initially to be used for this study complemented by competitive enzyme-linked immunosorbent assay (CELISA); however we eventually used the CELISA for all samples.

Herein, GOxNPs, hemin/G-quadruplex and PtNPs could form mimicking bi-enzyme cascade catalysis system to in situ generate dissolved O2 as coreactant in peroxydisulfate solution when the testing buffer contained proper amounts of glucose.