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The other four cDNAs lacked exon 2' (4.1R80 cDNAs) and hence give rise to short isoforms of protein 4.1R by using the downstream ATG2 present in exon 4 as a translation initiation site.
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Consequently, when using all these algorithms the false negative rate of CNVs detection is decreased, while the possible increase in false positives is addressed by using the following downstream filter criteria.
cDNA was then amplified by Race-PCR using the downstream GeneRacer™ primer and the upstream heavy chain primer IgG1 Nested (5'-GGCTCA GGGAAATAGCCCTTGACCAGGCATCC-3') or light chain primer Kappa Nested (5'-GTGAGTGGCCTCACAGGTATAGC-3').
As an initial step toward supporting this notion, we investigated in Goto-Kakizaki rats (GK rats, a model for non-obese type 2 diabetes) the possible involvement of PKA and its downstream effectors in angiogenesis by using the in vitro endothelial cell cultures and in vivo sponge implant angiogenic assays.
Finally, two types of output (dual synteny plot and circle plot) were obtained by using two downstream programs.
The nonsense cxcr3.2 hu6044 mutation is not likely to lead to a functional truncated protein by using a downstream AUG codon as a signal for translation initiation.
In the case of a C-terminal InDel, most of the protein product would be translated before encountering the variant while in the instance of a N-terminal InDel, there may be an opportunity to rescue major part of the protein by using a cryptic downstream start codon [ 47].
Putative transcripts located downstream of associations of telo boxes with site II motifs or TEF1 boxes were characterized by using sequences located downstream of these associations, Blastn and A. thaliana GB experimental cDNA/EST or Green Plant GB experimental cDNA/EST datasets.
As T cell activation requires receptor signalling, transcription factor activation, gene transcription, protein synthesis and protein trafficking, systemic abnormalities in these physiological processes in schizophrenia can potentially be traced in this model by using downstream effects of stimulation such as proliferation, cytokine production and gene transcription as readouts of cell function.
Correct integration of the deletion cassette was confirmed by PCR using the primers upstream and downstream of the cloning site.
The resulting PCR product (1.2 kb) was cloned into the suicide vector pDM4 via its NdeI and XbaI sites and confirmed by PCR using the upstream (p2309-1) andownstreamam (p2309-4) primers.
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