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Table 2 Promoters used in plasmids constructions Promoter Name Accession numbers (GenBank) S288C JPU CYC1 CYtochrome C KY704470 KY704471 Translationation Elongation Factor KY704476 KY704477 PhosphoGlucoIsomeraseerase KY704472 KY704473-PhosphoGlycerateycerate KY704474Y704474 KY704475 ADH1 Alcohol DeHydrogenase KY704468 KY704468.
Class 2 promoters (III and VI) contained a C to A transversion at −219.
NAT1 gene expression involves 2 promoters that generate at least 9 different transcripts, all with an identical protein coding sequence.
Type 2 promoters recruit the same factors except that in this case, the promoter elements recruit TFIIIC directly, without the help of TFIIIA.
The expression of β-galactosidase under the B. neotomae and B. suis biovar 2 promoters was considerably lower than the expression under B. abortus and B. suis biovar 4 promoters (Fig. 5B).
Examination of the sodC promoter activities using translational fusion constructs with E. coli β-galactosidase demonstrated that the B. neotomae and B. suis biovar 2 promoters were very weak in driving gene expression.
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Here, we have developed an iPSC-CM marking system using recombinant adenoviral reporter constructs with atrial- or ventricular-specific myosin light chain-2 (MLC-2) promoters.
In particular, the high activity levels of VvUb6-1 and VvUb7-2 promoters were verified by transient GUS quantitative assay as well as stable anthocyanin expression in sepal and corolla of transgenic tobacco.
We have shown that in contrast to AmphiVent1/2 and Xvent1/2 promoters, the promoter of VENTX is not Bmp-inducible.
Interestingly, quantitative analysis of relative start usage by the wild type, DPE-L1, DPE-L2 and DPE-L1/2 promoters in the in vitro transcription assay with HeLa nuclear extract revealed a differential effect on upstream, relative to downstream, start sites.
All 12 normal nasopharyngeal epithelial tissues showed unmethylated TFPI-2 promoters.
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