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This concentrate was fractionated using a Superose™ 12 (GE Healthcare, UK) gel filtration column (height 40 cm, diameter 3 cm) using ultra pure water as the mobile phase and fractions of 12 ml each were collected.
This concentrate was then re-filtered to 0.2 μM.
This concentrate was incorporated within a resorbable collagen sponge, activated with calcium chloride and autologous thrombin, and clinically implanted into the sinus floor of a patient.
Centrifugation was used to physically concentrate the particles, and then this concentrate was subject to a number of heating and cooling cycles.
This concentrate was mixed with equal volumes of the same buffered glucose solution used to dilute the retentate, filtered and freeze-dried.
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This concentrate is leached with aqua regia, which dissolves the platinum and palladium and leaves the other metals as solids in the leach residue.
Batches of Haemocomplettan P vary slightly in fibrinogen content, since this concentrate is a biological product fractionated from FFP (cryoprecipitate).
This concentrate is prepared in accord with ethnomedical traditions, where a decoction is made from the bark, and the solutes concentrated by freeze drying the decoction.
This protein concentrate was dried at 50 °C for 12 h and used for analysis.
This protein concentrate was characterizedfor proximate composition, colour analysis, water holding capacity, oil-holding capacity, foaming capacity, foam stability, amino acid composition, protein quality and thermal properties.
The number of EBV genome equivalents (geq)/ml of this virus concentrate was determined by semi-quantitative real-time PCR using primers directed to the BALF5 gene [27].
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