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We also label such UCAs as sparse UCAs [8].
We also label four ancestral genomes, the hypothetical 21-chromosome hexaploid ancestor, the rosid ancestor, the eurosid ancestor and the 9-chromosome Rosaceae ancestor reconstructed in [ 8] and, schematically, in [ 4].
To increase sensitivity in detecting length outliers that might be masked by similar whole-protein length, we also label regions of each multiple sequence alignment as conserved, N-terminal, C-terminal, or intermediate regions by requiring at most 20% gap content across reference proteins within conserved regions.
We also label with 10 μL mouse phycoerythrin (PE -conjugated monoclonal antibody for the mouse endothelial cell isolate and 10 μL human PE -conjugatedmonoclonal antibody for the remouseng cendotheliallate at final cellentratisolate 14 μg/mL for VEGFR1 and VEGFR2 (R&D).
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As the controls, we also labeled all these cells with isotype antibodies.
We also labeled the three sequences in some wild Glycine species and found that they widely co-localized with 45S rDNA.
As future pre-clinical applications may include lung evaluation for MSCs infusion in repair processes, such as broncho-pleural fistulae [23], and assessing cell migration into the lungs, we also labelled MSCs with PFC nanoemulsions, which can be detected with 19F MRI and MRS [9, 10].
Alternately, we also labeled uninfected DH82 cells with CFSE and seeded with DH82 cells infected with E. muris.
To reveal potential cytoskeleton changes associated with Plasmodium invasion, we also labeled the actin network with fluorescent phalloidin.
We also labeled the effector cells with CFSE before transfer and isolated the lymphocytes in the lung.
We also labeled cells with lacZ recombinant retroviral vectors injected at 2 days of age in newborn animals that were subsequently treated with either of the two drugs.
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