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By gradually changing the periods of the plasmonic nanoresonator array, we also design and demonstrate a plasmonic spectroscope for spectral imaging.
In addition to exploring variation in the number of DXZ4 monomers in an array, we also investigated sequence variation between different monomers.
In order to validate the array we also analyzed a sample of threespine sticklebacks from a Danish river that represents a mixture of marine and freshwater morphs.
As these SNPs were of key relevance to this array, we also included at least one or more tagging SNPs to cover those common variants present in the 1KGP database.
Using dual channel technology (measuring two groups of mRNA labelled with different colors simultaneously on the same array), we also pool human and mouse mRNA in equal parts as a control on the green channel.
For example, expression of COX Va mRNA in non-tumorous tissue could still be observed in subject No.3, 4 and 8. Using tissue core array, we also studied the immunoreactivities of COX Va in formalin-fixed, paraffin-embedded specimens and analyzed their pathologic significance in 250 consecutive patients with adenocarcinoma.
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Using two-dimensional protein analysis followed by mass spectrometry, phospho-flow fluorescence-activated cell sorting, and antibody arrays, we also identified changes at the protein level that contributed to MYC-dependent tumor regression.
Moreover, through screening the crRNA arrays, we also found the repression of arcAB expression lead to impaired cell growth even in both rich lysogeny broth (LB) medium and M9 medium (Figure 5a and b, Supplementary Figure S3B), which was consistent with a previous finding.
To further investigate the effect of different length silicon nanowire arrays, we also measured the dark current J V characteristics of the hybrid solar cells, which are shown in Fig. 5a.
In addition to the gene expression arrays, we also studied the impact of infection with recombinant NYVAC mutants on the maturation of DCs.
When comparing the expression levels for each miRNA in each replicate of microarray and qPCR-array, we also observed a higher false positive rate of differential miRNA expression in the microarray assay.
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