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The number of double-labelled cells was calculated relative to the number of cells positive for a comparative marker and expressed as a percentage.
The results are presented as vertical bars showing the low and high densities of each marker and expressed as the median ± standard error.
We assumed that each CySC contributes equally to the total Zfh1-positive pool and counted the number of Zfh1-positive cells (N) that were labeled with the clone marker and expressed this as a fraction N/43 where 43 was the average number of Zfh1-positive cells found per testis (see above).
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We generated double-heterozygous transgenic flies that harbor the xbp1-EGFP marker and express the wt-MYOC and each of the four mutants (R342K, Q368X, D380N and K423E) using the gmr-Gal4/UAS system [21].
We found in our model that the most powerful DCs that stimulate T cells were also positive for the Ly-6C and F4/80 markers and expressed MHC II strongly (Figure S5B).
A fourth, double-negative population - dubbed stromal - lacked epithelial markers and expressed PDGFRβ (CD140b).
The outgrowths generated were positive for both luminal and basal markers and expressed the appropriate genotype (Additional file 9D,E).
We next studied the gene and protein expression of cardiac markers, finding that zebularine-treated cells highly expressed cardiac-restricted markers and expressed low levels of pluripotency factors.
The evaluation, annotation and classification of genomic markers and expressed transcripts would be of great utility for both functional genomics and systems biology research in plants.
Conversely, those cell lines which were relatively insensitive to erlotinib lacked those epithelial markers and expressed proteins characteristic of mesenchymal cells, including vimentin, fibronectin and Zeb-1 and exhibited a more fibroblastic, scattered morphology.
In this work, we proved that Pax6 cells did not colocalize with the glial marker GFAP and expressed the neuronal marker HuC/D.
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