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In our work, natA and natG had background transcript levels in all conditions.
Background transcript levels for some of these genes (e.g., natA, natG, and fraC) might reflect low abundance and/or high stability of these proteins in vivo.
Very low, almost background transcript levels were detected for W109669 (Additional file 6D), suggesting that this gene is most likely involved primarily in defense responses, whereas W100630, W100577 and W108715 are also expressed during plant development.
Other psb genes tended to have higher signal intensities in vegetative cells, but with the exception of psbH, psbJ, and psbY that had background transcript levels in all experiments were usually still transcribed in heterocysts.
Nevertheless, the impression given is that fkh-9 transcript b is the functionally important transcript but the distribution of background transcript noise, arising from either cryptic promoter activity (fkh-9a) or aberrant trans-splicing (fkh-9c), is influenced by transcript b regulatory elements.
Similar(55)
Sequencing deeply, we detect both miRNA that function in brain and miRNA expressed as "background" transcripts.
A gene that is moderately expressed in a small fraction of cells in a sample might be indistinguishable from the background transcripts of the whole sample.
However, in the W64A background the transcript profiling and proteomic data showed enolase 1 accumulation was higher in o2.
In the GmFLD transgenic A. thaliana (Col or fld background), FLC transcript levels decreased and the floral integrator genes FT and SOC1 increased significantly.
In the transgenic plants in Col background, FLC transcript level decreased significantly while FT and SOC1 were up-regulated, the SOC1 level were especially increased.
In phm>CTCF RNAi background the transcript levels of dib, sad and nobo were 2-5 folowerwer in phm>CTCF RNAi larvae at the time points of maximal induction (Fig. 2) and we observed almost no induction of spok, which is one of the genes of the so-called Black-Box that has been suggested to be a rate limiting step in ecdysone synthesis (Warren et al., 2009).
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