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All genotypes were determined clearly by this marker and only Kasalath had the yield-positive TGW6 allele among our breeding materials (Fig. 8a).
Such is the case despite the hypothesis that a broad range of functions mediated by this marker are probably assumed by other Ly6 proteins in humans.
Moreover, the GLS resistant allele discriminated by this marker was conserved within DAS-001 genetic background and not revealed among GLS susceptible lines (Additional file 7E).
We now set out to elaborate on the information provided by this marker in a variety of diseases and larger patient cohorts.
The CT-value of p1B reaches a plateau when less than 50 Mcellsells are present, indicating that a sensitivity of 50 breast tumour cells can be reliably detected by this marker.
The CD3 immunohistochemistry for T cells showed that about 50% of the cells in the WT spleen were positive, whereas in the Tg spleen over 90% of the cells in the infiltrate were labeled by this marker.
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However, some species cannot be unambiguously barcoded by solely this marker due to low evolutionary rates.
Differential diagnosis and antibiotic treatment as well can be improved by using this marker [ 18, 19].
All constructs were cloned while maintaining the HisTag included in the vector, thereby allowing the possibility of identifying these genes by using this marker.
By contrast, this marker for oxidative DNA damage was significantly increased in mtDNA from cells treated with palmitic or stearic acids but not in those treated with the monounsaturated oleic acid.
These strains were generated by insertion of a PCR fragments with a URA3 selective marker to the C-terminus of Med15, followed by looping out this marker through homologous recombination [13].
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