Exact(4)
Avery and his research team obtained mixtures from heat-killed virulent bacteria and inactivated either the proteins, polysaccharides (sugar subunits), lipids, DNA, or RNA (ribonucleic acid, a close chemical relative of DNA) and added each type of preparation individually to avirulent cells.
The obtained mixtures were pressed at the pressure of 30 GPa.
The obtained mixtures were taken in a crucible and calcinated in air for 40 h, after every 6 h the products were grounded and recalcinated [31, 32].
The obtained mixtures (clear, transparent and colorless in the absence of sepiolite and light brown in its presence) were introduced in capped polypropylene bottles and allowed to homogenize for 16 hours under magnetic stirring at RT.
Similar(56)
The obtained mixture was separated and purified to examine the decomposed products.
Tigecycline, in a solid state, was mixed with CHA powder and the obtained mixture was compressed into tablets.
Aggarwal, Singh, Sarin, and Husain (2009) considered the case of components assuming equal volume fractions and obtained mixture designs in orthogonal blocks using F-squares.
The composite was prepared through the blending of a PVA gel with SA, and then the obtained mixture was crosslinked by formaldehyde (HCHO) and calcium ion (Ca2+).
Prescott and Draper (2004) obtained mixture component amount designs via projections of standard mixture designs, viz., the simplex-lattice, the simplex-centroid and the orthogonally blocked mixture designs based on latin squares.
The obtained mixture was purified by centrifugation.
The obtained mixture was refluxed for 6 h.
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