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Karvelis, T. et al. Rapid characterization of CRISPR-Cas9 protospacer adjacent motif sequence elements.
(b) The SV40 early region promoter comprises two functionally distinct nucleotide sequence elements.
Khvorova, A., Lescoute, A., Westhof, E. & Jayasena, S. D. Sequence elements outside the hammerhead ribozyme catalytic core enable intracellular activity.
The diversity of the generated tectons ranges from elastine-, resilkn, silk- to epitope sequence elements.
When placed between an enhancer and promoter, certain DNA sequence elements inhibit enhancer-stimulated gene expression.
We demonstrate simple pulse sequence elements for eliminating this unwanted residual signal.
Possible functional relationships of the core sequence elements were tested by systematically exchanging sequences between the two ribozymes.
Peaked promoters were found to contain location-specific sequence elements; conversely, broad promoters were associated with non-location-specific elements.
The −35 and −10 sequence elements are in bold, the transcriptional start site is underlined.
The assumed −35 and −10 sequence elements are in bold, the transcriptional start site is underlined.
Conserved sequence elements are highlighted and identical residues were showed in the consensus line.
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