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In order to understand the molecular phenotypes of rhesus spermatogonia in the context of classical descriptions of nuclear morphology (i.e. Adark, Apale, B spermatogonia), expression patterns of GFRα1, PLZF, NGN3 and cKIT were evaluated using colorimetric immunohistochemistry in adult testis sections counterstained by the periodic acid-Schiff method and hematoxylin.
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HDAC inhibition activity of conjugates 1 and 2 was evaluated using a colorimetric assay.
The cytotoxicity of PS-QD micelles on J774A.1 cells was evaluated using a colorimetric MTT assay kit.
In this study, the enzymatic activity of lysozyme in the core of polyion complex (PIC) micelles, which were formed from egg white lysozyme and poly ethylene glycol)–poly(α,β-aspartic acid) block copolymer (PEG-P(Asp)), was evaluated using a colorimetric method.
TSM1 and primary cultures of neuronal cells were incubated in the presence of increasing concentrations of MPP+ iodide (from 0.1 to 2 mM) for 15 h and the cell viability was evaluated using the colorimetric MTS assay (Figure 2A).
Caspase-3 and −8 were evaluated using a colorimetric assay.
Cell viability was evaluated using a colorimetric water-soluble tetrazolium salt (WST-1) cell proliferation assay.
The effects of HHS on cell viability were evaluated using a colorimetric MTT assay.
The inhibitory properties of the analyzed compounds were evaluated using a colorimetric indophenol assay.
Elastase activity, evaluated using the colorimetric assay described, is demonstrated for normal and pancreatic cancer tissue in Figure 5.
Cell viability in a 96-well culture plate was evaluated using the colorimetric MTT assay (Chemicon International , Inc Temecula, CA, USA) according to the manufacturer's instructions.
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