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Cells were incubated with (80 µg/mL) or without (control) sc-68920 antibody for 15 min on ice, then PAB binders at concentration 10 µg/mL were added and left to incubate for 30 min. Binding of PAB variants was detected by streptavidin-PE conjugate.
None of the variants was detected in the Nova Scotia or HapMap control DNA samples or in dbSNP.
Generally, a broad range of different A-type rif variants was detected in each experiment at similar frequencies, indicating that there is no clear dominance of single variants in any of the stages (Fig. 5, Table 2).
For example, a relatively high proportion of subfamily A variants was detected in carriage isolates.
Importantly, no peptide unique to canonical H2A or any other H2A variants was detected.
Autophosphorylation of hMyo3A-KD variants was detected by incorporation of P using [γ-P]ATP.
Similar(43)
FS is amenable to current structural variation detection methods, and variants were detected.
S. Typhimurium and its variants were detected rapidly and accurately.
However, several size variants were detected of NecC produced by T. discophora under native conditions.
Homozygous or hemizygous variants are detected by prior mixing with wild-type DNA.
No escape variants were detected after therapy.
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CEO of Professional Science Editing for Scientists @ prosciediting.com