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Inhibitors in dried material pose a serious challenge because fresh tissue is often not available.
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This theory enables determination of drying-induced stresses and elastic plastic deformations arisen in dried materials.
Their concentration in crude dried material is 21,76 mg per gram.
They found that freeze-drying samples reduced recoveries of OCPs and PCBs, probably due to tighter binding and occlusion of residues in the dried material.
An extraction of Anethum, prepared from fresh material, amplified and sequenced cleanly, suggesting that secondary metabolites in the dried material (which were not effectively removed with a commercial DNA purification kit), rather than suboptimal PCR parameters (identical for both samples), reduced amplification efficiency and inhibited sequencing.
Less removal capacity of carbonized biomass in comparison to dried material may be due to its inefficient adsorption property with higher Cu II) concentration.
The mass of dried material in extractor, the extraction time and CO2 mass flow rate were kept constant during experiments.
An NMR sample was prepared by lyophilizing 4 mg of purified F. tularensis capsule polysaccharide against 3 changes of D2O and dissolving the dried material in 0.5 mL of 99.96% D2O from a freshly broken ampoule.
Break new reeds in gradually, so the dried material gets used to being wet again.
The dried material was carbonized in muffle furnace in the absence of air at 500°C for about 4 h.
But even on the Kew sheet, it is difficult to make out intact calyx lobes and verify other characters because the dried material is in poor condition and mounted on a sheet.
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