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In each sample, we measured 10 points to obtain average Raman intensity as the reference used in the SERS enhancement factor calculation.
In order to analyze the Fe doping of prepared sample, we measured the magnetization versus applied magnetic field curves for the Zn1 − x Fe x O NDs at with different compositions.
In each sample we measured the abundance of the housekeeping gene RPS16, and normalized the data using the 2̂- ΔΔCt) method [45].
To validate the microRNA expression in each sample, we measured the expression of 171 microRNAs by using a qRT-PCR platform: TaqMan microRNA Assays (Applied Biosystems Inc).
In each blood sample we measured melatonin, cortisol, TRH, TSH, free thyroxine, GH, IGF-1 and IL-2.
In the 2008 2010 cross-sectional sample we measured IgE for the first time and collected additional information on smoking exposure history, household exposures, asthma, eczema and rhinitis.
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To demonstrate the capability of the micro-XRF setup for in-vivo measurement of trace elements in biological samples, we measured cobalt (Co) accumulated in leaves of duckweed floating on a Co solution surface.
To gauge whether our PSRP 91 gene TaqMan qPCR assay provides equivalent expression measurements from both snap-frozen and paraffin-embedded samples, we measured gene expression in the tumor-matched samples of the 18 patients at the Medical College of Wisconsin who had tumor tissue preserved by both snap- freezing and the standard FFPE.
For the layered samples we measured a concentration of strain within the weak layer.
For all samples, we measured the reflectivity of both pristine and grafted layers, as a reference.
For the two powdered samples, we measured emissivity for increasing θ under vacuum (P < 0.8 mbar), at surface temperature of 100 °C. Figure 6 shows the spectra we measured for a Millbillillie sample.
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