Sentence examples for the samples were achieved using from inspiring English sources

As indicated in Table 1, in El Salvador and Guatemala City, the samples were achieved using two or three seeds and the highest number of waves ranged between 12 15.

Derivatization of the samples was achieved using a 2-step process.

Elution of the sample was achieved using methanol/methyl-tert-butyl ether (1 : 9, v/v).

Further purification of the tumour samples were achieved using trypsinisation until the contaminant mesothelial cells were seen to detach, while the tumour cells remained in situ.

Chromatographic separations of prepared samples were achieved using a Shim-pack XR-ODS column (2.0 mm i.d × 100 mm) maintained at 40°C.

Chromatographic separations of prepared samples were achieved using a phenomenex ® Luna C18 column (5 μm, 2.0 mm i.d × 50 mm) maintained at 40°C.

Chromatographic separations of prepared samples were achieved using a Phenomenex Kinetex 2.6 μm XB-C18 column (2.10 mm i.d × 50 mm) maintained at 40°C and coupled with a 0.5-μm biocompatible inline filter.

Quantification of VTG in the plasma samples was achieved using an established homologous carp enzyme-linked immunosorbent assay (Tyler et al. 1999) that has been validated for use with a wide variety of cyprinid fish (Tyler et al. 1996).

DNA extraction from the Sputolysin-treated sputum samples was achieved using the Puregene DNA isolation kit (Qiagen), according to the manufacturer's instructions.

The best performance for saliva samples was achieved using the Immuno-Rápido HBsAg® assay in the G I and II samples.

The quantification of TOrCs in all samples was achieved using a calibration curve with at least nine points and an R2 no lower than 0.990 and typically above 0.995.