Sentence examples for buffer was determined with from inspiring English sources

The strain related to a reference zone chosen in the GaAs buffer was determined with a spatial resolution better than 1 nm, by means of geometrical phase analysis of the HR-TEM images [13, 14].

The feces of challenged mice were collected prior to challenge (day 0) and daily for 8 d after the challenge, and the presence of RV antigen in fecal samples suspended in TNC buffer was determined with ELISA as previously described.

Salivary mutans streptococci and buffer capacity was determined with Dentocult® SM - Strip mutans and Dentobuff® Strip, respectively.

The yield of sorted nuclei in sort buffer (PBS) was determined with a hemacytometer, and 50 200 K nuclei were used for each ChIP.

Recently, the number of P. ostreatus laccase isoenzymes in buffered and non-buffered media was determined with the initial pH adjusted to 3.5 in both culture media.

Furthermore, total protein was extracted from lumbar CLC-rich NPs from non-chondrodystrophic and chondrodystrophic dogs using radioimmunoprecipitation assay (RIPA) buffer; protein concentration was determined with a Lowry assay.

The integrity of the total RNA was checked by electrophoresis in 1% agarose gel in Tris-acetate-EDTA (TAE) buffer and quantity was determined with a NanoVue™ Spectrophotometer (GE healthcare).

The resulting pellets were homogenized in 500 ul of buffer and protein concentration was determined with a BCA protein assay.

Briefly, cellular protein was extracted from mouse liver using lysis buffer, and protein concentration was determined with a BCA protein assay kit (KeyGEN, China).

Unbound iron and sulfide was removed by desalting on a 10 ml Sephadex G-25 column (GE Healthcare) equilibrated in buffer A. Protein concentration was determined with the Microbiuret method at 545 nm [ 36].

Enzymes peroxidase, lactoperoxidase and alkaline phosphatase in phosphate buffer were tested and activity was determined with commercial reflectometric strips.