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It is shown that the use of anionic marker results in a significantly better analytical parameters, as compared to measurements with cationic marker.
Caspase-3 bring a crucial apoptosis marker; results suggest that surface conjugation of targeting ligand will be detrimental to cancer cells.
These immunohistochemical marker results are similar to conventional DCIS and there were no differences in expression patterns between the columnar epithelial cells and dimorphic cells.
For each marker, results are expressed as a mean number of positive cells per mm2 of epithelium +/− SEM.
This indicates STR locus saturation, which seems to occur more rapidly in case of tri- and tetranucleotide markers (the age estimate for the CF clade based on tri/tetra marker results is 42,200 years, considerably lower than the estimate of 64,700 years based on penta/hexa marker results and the estimate of 68,900 years based on SNP marker results [24]).
Our most interesting finding is that our analysis of an identical set of marker results implicated almost entirely distinct genomic regions under the two methods.
Direct integration in WT haploid strains (BY4741) and selection for the URA3 marker results in yeast colonies that are red following establishment of the selectable marker.
Therefore, we generated haplotypes and tested for association with our outcome measure (peak anti-HBs level) and compared these findings to previous single marker results.
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In each marker result, the yield-positive allele of the genes was shown with a green letter.
Anti-telomere PNAs, transfected into human fibroblasts along with a selectable marker, resulted in a significant reduction in colony size and elicited cell death by apoptosis.
To obtain this goal, yhcS was replaced by a chloramphenicol resistance marker resulting in strain SZ59 (yhcS::cat) and ywpE by an erythromycin resistance marker (SZ60: ywpE::erm) as shown in Figure 2A and 2B.
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