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2,842 of those genes were successfully aligned to the Cattle QTL database (http://www.animalgenome.org/cgi-bin/QTLdb/BT/index) (Table S3).
The approach was applied to five different hybridomas producing human monoclonal antibodies and variable regions for both γ and μ heavy chain and κ and λ light chain genes were successfully cloned.
Using the method of EM with KF, 25 cell cycle-regulated key genes were successfully clustered into three functionally co-regulated groups.
Both genes were successfully integrated into the H. pluvialis genome, either separately or together, using the endogenous norflurazon resistant mutated gene of phytoene desaturase as a selection marker.
After scanning for InterPro domains, 280 of these genes were successfully annotated, and 215 of them could be assigned to Gene Ontology (GO) terms.
The lead candidate molecule was generated via a novel antibody discovery process, and the selected IgG variable region genes were successfully humanised and reformatted as a human IgG γ1 Fab fragment.
These results confirmed that the pct and bktB genes were successfully expressed in E. coli JM109.
The cloned genes were successfully expressed in both E. coli BW25113 and C. acetobutylicum ATCC 824.
The customized DHQase genes were successfully expressed in E. coli, and functional DHQases were obtained.
On a benchmark including 120 pairs of human and mouse genomic sequences, most of their encoded genes were successfully identified by our program.
Even if the symbionts took, even if the controlling genes were successfully added, would this make a difference to us? Probably not.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com