Exact(16)
In a second assay, the formed composite monolayers became thrombin-sensitive by immobilization of an RNA anti-thrombin aptamer.
In a second assay, duodenal flow and ruminal DM digestibility were calculated from the duodenal and fecal concentration of either marker.
These observations were confirmed in a second assay based on the quantitation of hydroxyproline in procollagen by reverse phase HPLC (Fig. 3k) and provided strong evidence that mTORC1 is a key signaling node involved in mediating the potent fibrogenic effects of TGF-β1.
The same sera were then tested in a second assay (TZM-bl assay) that included 6 clade C viruses and 2 clade B viruses.
In a second assay of leptin sensitivity, we next tested whether leptin could stimulate acute phosphorylation of STAT3 in neurons of the mediobasal hypothalamus among the four groups of mice[10], [13], [38].
In a second assay, leaf explants of F2, BC1, P1, P2 and F1 plants were tested as explained above.
Similar(44)
As TMRM was used to both record and stimulate mPTP opening in this assay, a second assay was developed to confirm the results.
Therefore, a second assay in the trnL-trnF intergenic spacer was applied, to distinguish this Senecio sample from C. officinalis.
In a first assay, the two extreme sizes alleles [CA 8 and (CA 15] were compared.
In a third assay, we stained MIN6 cells with propidium iodide and counted the number of apoptotic plus necrotic cells.
In a first assay, SLBs were composed of 99.4% POPC, 0.5% biotin-cap-DOPE, and 0.1% Texas Red-DHPE.
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