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The Yates χ test and P-value were used to evaluate disparity of staining performance between cytology and histology groups.
In summary, we present a general approach to characterize the brightness and staining performance of nanoparticle SERS tags in the context of a surface binding assay.
When 3 markers are evaluated (last row in Table 2), the triple staining performance in cytology and histology slides is very similar (P=0.92).
The staining performance for cytology and histology slides as shown by sensitivity, specificity, PPV, and NPV are demonstrated in Table 2.
In contrast to class II tetramers using OVA-derived peptides, 2W I-Ab tetramers, which stain CD4+ T cells that are specific for the 2W I-Abide, offer a betetramersning performance.
Many factors, including low expression of cognate proteins, poor binding affinity or specificity of the antisera, and high background signal and other technical factors can complicate immunohistochemical staining performance.
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By applying M3T copolyacrylate, fluorine-free silicone based material to masonry and fabrics, good anti-stain performance was achieved.
Good anti-stain performance has been obtained on the treated substrate, while the copolyacrylate with molecular weight of 80,000 and concentration of 20 wt%, With increase of tris-trimethylsilypropyl methacrylate (M3T) ratio, the coating critic surface energy decreased, better anti-stain performance was achieved.
Research work has been done systematically on the effects of the ratio of M3T unit in the copolyacrylate, copolyacrylate concentration in coating formulation, copolyacrylate molecular weight, and solvents on coating anti-stain performance.
We discuss the impact of different k LSC for staining patterns classification performance.
We would expect Gram staining to increase test performance as found in the analysis.
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