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All of the experimental constructs were able to express successfully in yeast cells (data not shown), and panel a in Figure 1B shows that all of the cotransformants were also able to grow on the SD/-Leu/-Trp plate.
After checking that all of the constructs were able to express successfully in yeast cells (data not shown), we found that all of the cotransformants were able to grow on the SD/-Leu/-Trp plates (panel a of Figures 6B, 7B and 8B).
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While genes designed to match host bias or maximizing CAI have expressed successfully in many instances [8], [9], clear relationships between these practices and expression are lacking.
Streptomyces cyaneus CECT 3335 laccase with a C-terminal His6 tag was expressed successfully in E. coli.
Several classes of shells have been loaded with exogenous proteins and expressed successfully in industrial hosts.
Two recombinant proteins were expressed successfully in wild-type Klebsiella pneumoniae.
The assembly was expressed successfully and characterised in its active form, displaying improved electrochemical properties.
The recombinant vectors pColdTF-lsrB and pColdTF-luxS were expressed successfully in E. coli BL21 and BL21∆luxS cells.
The three different HSL isoforms were expressed successfully in Sf9 insect cells and purified (Figure 1).
Using these spectra, we calculated the absorbance difference spectra (Fig. 1B,C), which indicated that PrB and PrV were expressed successfully.
All ITvar9 Pfextracellularlular domains were expressed individually, except for the first CIDR, which could only be expressed successfully as part of the NTS-DBL1α-CIDR1γ di-domain (Figure 1).
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CEO of Professional Science Editing for Scientists @ prosciediting.com