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Furthermore, Western blot analysis indicated the incubation of cells with either vardenafil or tadalafil for 72 h did not alter ABCB1 protein expression.
Western blot analysis indicated the antibody recognizes the 120 kDa E-cadh present at 30% and 50% epiboly and at 24 hpf (Figure 4B).
Western blot analysis indicated the successful expression and secretion of all CipA variants by the recombinant strains.
Western blot analysis indicated the presence of Twinkle in isolated mitochondria and chloroplasts of Arabidopsis (data not shown).
Western blot analysis indicated the presence of processed secNluc in the medium, while Nluc without a secretion sequence was detected only in cell lysates (Supplementary Figure s11).
Southern blot analysis indicated the increased levels of MRP and ARA expression resulted from gene amplification and that MRP was first amplified in the E100 subline and ARA in the E200 subline, suggesting that the two genes were not initially co-amplified.
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Western blot analysis indicates the analogues containing hydroxyl group inhibited expression and tyrosine phosphorylation of EGFR.
Western blot analysis indicates the presence of eEF1γ in mitochondria-enriched HeLa cell extracts (fig. 4C).
Southern blot analysis indicates the presence of a met-like gene also in the Wolbachia strain wUni, which is known to induce parthenogenesis in the parasitic wasp Muscidifurax uniraptor (data not shown).
In the present study, the serum levels of C3 and its fragments C3a were over-represented in diabetic serum by western blot analysis, indicating the activation of complement system.
Northern blot analysis indicates the desired tissue specificity of these genes.
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