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The commercial glucometer shows that the blood glucose concentration of mouse is 0.792 g L−1.
Without the injection of glucose solution, the blood glucose concentration of mouse is 0.756 g L−1 (measured by a commercial blood glucometer), and the outputting piezoelectric voltage is around 0.16 V.
This study evaluated the in vitro effect of PHA degradation product 3-HB and its derivatives (collectively called 3-HB derivatives) on cell apoptosis and cytosolic Ca2+ concentration of mouse glial cells.
Results of both PMIDA Fe1−xMnxFe2O4 linked ELISA revealed that the enhancements in absorbance during the catalysis of enzyme substrate were linearly proportional to the concentration of mouse IgG within the range between 0.1 μg/ml and 2.5 μg/ml.
The same concentration of mouse IgG (Chemicon International) was used as a negative control.
The total IgG and IgA concentration of mouse vaginal lavage was determined using a multiplex mouse immunoglobulin isotyping kit (Millipore, Billerica, MA) following the manufacturer's instructions.
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Figure 5 shows the plasma genistein concentration of mice fed these diets compared with that of F344 and S-D rats.
The impedance based response of the two-terminal device revealed a very high sensitivity with low concentrations of mouse monoclonal IgG, sarcosine, cadmium sulphide (CdS) and potassium chloride (KCl) at pico mole levels.
Concentrations of mouse IFN-γ in the supernatants were determined by ELISA (eBiosciences).
Serum IgG concentrations were quantified from a standard curve prepared from known concentrations of mouse IgG (SouthernBiotech).
The plasma concentrations of mouse SAA were measured with an ELISA that showed no cross reactivity towards the hSAA protein (data not shown).
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