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Samples of kidneys, liver, longissimus lumborum, and triceps brachii were collected and evaluated for concentrations of 1,25- OH 2 1,25- OH 2
Right and left atrial blood samples were evaluated for concentrations of coagulation markers, including intact fibrinogen, fibrinopeptide A, D-dimer, prothrombin fragment 1+2, and thrombin-antithrombin III complex.
The matrix effect was then evaluated for concentrations around those previously obtained, using five matrix-matched 226Ra standards, with increasing concentrations of Ca (1, 2, 5, 10, and 20 μg g−1) and Mg (0.25, 0.5, 1.25, 2.5, and 5 μg g−1), and comparing them with a standard without Ca and Mg, at the same 226Ra concentration (27.5 fg g−1).
In this large epidemiological study, > 2,000 human blood samples were evaluated for concentrations of PCBs, PCDD/PCDFs, and p,p′-DDE (Kočan et al. 2004).
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The quality and quantity of the RNA samples were evaluated for concentration and purity using a NanoDrop ND-1000 Spectrophotometer (NanoDrop; Wilmington, DE), and for integrity by gel electrophoresis using the FlashGel® RNA cassette system (Lonza; Rockland, ME).
After resuspension of RNA in nuclease-free water (Gibco), the samples were measured and evaluated for concentration and purity (260 nm/280 nm ratio) using a BioPhotometer (Eppendorf), in which values between 1.7 and 2.0 for 260/280 nm ratio were considered optimal.
Purified DNA fragments were checked on 1.5-2% agarose gel stained with Gel-Red® dye solution, then evaluated for concentration by detecting absorbance at a 260 nm wave length at a Nano Drop device (Thermo Scientific®).
Its effectiveness was evaluated for the concentration of skim milk and a whey protein concentrate with 80% (w/w) protein on a dry-matter basis (WPC80).
The semen collected by urethral catheterization from eight male cats was evaluated for sperm concentration and motility and subsequently diluted with a TRIS-based extender to the concentration of spermatozoa 10 × 106/mL, 5 × 106/mL, and 1 × 106/mL.
The dose response was evaluated for fixed concentration of mitotic cyclin Clb2. Figure 5 shows the predicted response curve for the fractional Cln1/2 concentration, which varied depending upon the concentration of Clb2.
The tablet was further evaluated for plasma concentration of INF-β in the New Zealand White rabbit, and compared to a known subcutaneous formulation.
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