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A set of properly ordered conditional pdfs, that uniquely characterizes the target joint pdf, in the first approach and a set of target marginal pdfs and a target SRCC matrix, in the second approach, are estimated from available experimental data.
Participants should therefore respond quickly when the same color characterizes the target as did so in the preceding trial.
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UHPLC-ESI MS/MS was adopted to characterize the target constitUHPLC-ESI MS/MSicinale.
Extensive purification and NMR studies were necessary to characterize the target compounds and the results of these investigations are reported here together with the synthesis.
Put it simply, the ultimate objective of target decompositions is to decompose a radar matrix into the weighted sum of several specific components, which can be used to characterize the target scattering process or geometry information, as shown in (2)–(4).
We have previously demonstrated that this method can be used to characterize the target epitopes of monoclonal antibodies [6], [7], [8], [9], [10], [11], [12], [13], [14] and, more recently, we have also applied this technology to polyclonal serum [15].
Next, we characterized the target of TA10.
One can characterize the target profile of a bioactive compound by following the CCCP approach.
In conclusion, there is clearly a need to characterize the target organ stroma with the same level of detail dedicated to the primary tumor stroma.
To further characterize the target masses, product ion scans (MS/MS) were collected [collisionally activated dissociation (4), collision energy (30 eV), cell exit potential (15 V)].
To confirm this, we next characterized the target of another recently obtained scFv, which was also observed to be conformation specific (own unpublished observations).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com