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A control native CN sample (i.e., time 0) was also prepared by adding 50 μL of 10 mM HEPES buffer (pH 7.6) to 200 μL of 0.40 μg/μL CN solution in 10 mM HEPES buffer (pH 7.6).
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Bean dregs-based activated carbon/copper ion redox active electrolytes supercapacitors (BDACCIS) were prepared by combining bean dregs-based activated carbon with copper ion redox active electrolytes, which were prepared by introducing NH4NO3 (NN) auxiliary electrolytes into Cu(NO3 2 (CN) solutions.
During sintering WC in the shape of platelets formed in (Ti,W)(CN) solid-solution ceramics, which were synthesized from milled mixtures of oxides with carbon.
In this method, various concentrations of MEPA or standard solutions (1.0 ml) were mixed with 2.5 ml of potassium buffer (0.2 M, pH 6.6) and 2.5 ml of Potassium ferricyanide [K3Fe (CN) 6] (1 %) solution.
The percentage of degradation of CN- aq) has been measured by applying the following equation: %Degradation = (CN- aq)/Co × 100, whase Co is the initial concentration of CN-(aq) and C is the concentration of uncomplexed CN-(aq) in solution.
The effects of the concentration of TPP (CTPP) and NaCl (CNaCl) in the cross-linking solution on CN were studied by infrared spectroscopy, ninhydrin assays and elemental analysis.
For the detection of l-serine, electrochemical studies such as CV, DPV, and LSV studies were performed with the sample solutions in phosphate buffer solution at CN electrode and CV, SWV and LSV studies were performed for l-phenylalanine detection.
A stock solution of CN-A was prepared in absolute ethanol at 20 mg/ml.
A stock solution of CN-A for administration was prepared in dimethyl sulphoxide at 100 mg/ml, and rapamycin was dissolved in ethanol at 1 mg/ml.
Then, CN was mixed with polystyrene solution using mechanical stirrer followed by sonication.
There is one limit cycle in the region where the Hamiltonian,Esay, is positive, i.e., a solution of type cn, and six limit cycles, three double values, in the region whereEis negative, solution type dn.
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