Primer concentrations were adjusted to give balanced amounts of products and peak heights, concentrating on the lineal SBE reaction[54].
The EPN concentrations were adjusted to 10, 20, 30, and 40 IJs/larva.
albicans SRCA4 >128 Protein concentrations were adjusted by the results of colorimetric assay as described in "Materials and methods".
Next, mRNA concentrations were adjusted to 400 ng/μl by diluting the crude total mRNA extracts with RNase-free water.
The nitrate concentrations were adjusted with a sodium nitrate and potassium chloride solution (Na+/K+ weight-ratio of 1 27).
The fungal spores concentrations were adjusted to 5 × 105 spores/mL using a haemocytometer before each test.
Primer concentrations were adjusted specifically for microdevice amplification, resulting in well-balanced short tandem repeat (STR) profiles.
Dietary concentrations were adjusted for each sex on a weekly basis except during gestation and lactation, to provide the intended mg/kg/day PVA levels.
Both fibroblast and bacteria concentrations were adjusted to 1.0 × 105 cells/ml and incubated under static conditions at 37 °C in darkness.
The inoculants were initially prepared in DYGS medium (Rodrigues Neto et al. 1986) and, after growth for 48 h, cell concentrations were adjusted to 108 mL−108
Rumen-degradable protein concentrations were adjusted by varying the supplies of ground vs. steam-flaked corn grains, and untreated vs. heat-treated soybean meals.
