Exact(15)
Lundh et al. [19] showed in thyroid cells assays that the relative biological effectiveness (RBE) of 123I versus 131I was about 5-fold, resulting in α value for 123I ranging from 1.9 to 4.9 Gy−1.
However, Lundh et al. [19] showed in thyroid cells assays that the relative biological effectiveness (RBE) of 123I was about 5-fold higher than that of 131I, and thus an uptake reduction induced by a low 123I activity cannot a priori be rejected.
Specificity of the clones was confirmed by carrying out T cells assays with Ac1-11 peptide loaded APCs.
Thus, although artificial, the HeLa cells assays suggest a cooperation of the promoter with distant enhancer regions in the expression of the gene.
In the available studies the source of cells, assays used, culture conditions, and the extent and timing of gene expression profiling have been variable, precluding a comparison of the effects of different AML oncogenes.
To determine the effect of EGF4KDEL on malignant mesothelioma cells, assays measuring protein synthesis via H-leucine incorporation were conducted.
Similar(45)
(C) Cell proliferation rate in RNASEH2C-knockdown cells compared to control cells assayed by CCK-8 kit.
Fig. 7 Apoptosis induced by scFv apoptin in Raji and Jurkat cells assayed by Annexin-V/PI staining.
The uptake efficiency of nanoparticles by cells, assayed on 48 h after incubation, was higher at lower nanoparticle concentration.
Three-omics single-cell assays also became possible.
Few in vitro cell assays can be used to represent a particular step of metastasis.
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