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To identify the localization of OCT1 in tumor tissue, we subsequently evaluated protein expression by fluorescence microscopy.
We evaluated protein expression of 35 candidate markers using immunohistochemistry on a tissue microarray (TMA) composed of an independent set of 249 ccRCC and 25 chRCC.
In this study, we have evaluated protein expression differences to identify potential biomarkers of disease progress from oral leukoplakia to OSCC in order to gain further insight into potential mechanisms underlying these transformations.
Both CD25KO and CD25/IL-17 CD25/IL-17gher expression of IFN-γR at 4 W compareDKOo IL-17KO; but greater mRNA levels were observed in CD25/IL-17 DKO LG compared to CD25KO at 8 and 12 W. Immunostaining evaluated protein expression at 4 and 8 W because thade ages higherexpression differences.
As opposed to the five studies already mentioned, we evaluated protein expression not only irrespective of the cellular localization of the antibody but also on different cellular compartment (membrane or cytoplasm) separately, assuming that this phenomenon might be related to divergent functional properties of the genes.
We next evaluated protein expression levels of AKT/mTOR signal pathway molecules in the 7 SCLC cell lines by Western blot analysis.
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However, it needs to be considered that the present investigation evaluated protein expressions and enzyme activities in whole lung homogenates, but not in single cells.
To determine causes of the abnormal cell cycle found with GIPC1 suppression, we used Western blotting to evaluate protein expression of known cell-cycle check-point regulators found differentially expressed in the microarray analysis.
A quantitative method was performed to evaluate protein expression levels, and to check the origin of common and unique peptides from M. tuberculosis and M. smegmatis GMPS proteins.
To evaluate protein expression profile and to quantify proteins present in seminal plasma from men with spinal cord injury (SCI) and healthy men without SCI.
We expressed full-length (∼170 kDa) HCNCp under its own promoter with a small C-terminal epitope-tag to evaluate protein expression profiles.
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