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The valine at position 8 of the human sequence is as suitable to bind to RT1.BL as the isoleucine at position 8 of the rat sequence.
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The evaluation of reactivity suggests that functionalized CNTs substrates, in particular those carrying –NCS groups, are suitable to covalently bind probe molecules such as proteins and oligonucleotides, thus opening up the possibility of future application in genomics and proteomics fields.
One of the most active researches in fullerene separation is to find suitable receptors to bind fullerenes and then release them through host guest interactions based on supramolecular chemistry to obtain pure products.
This may be explained by the observation that the catalytic domain of the exonuclease is tethered via a flexible linker to the polymerase (Ozawa et al, 2008) and may therefore not be always in a suitable position to bind the 3′ end of the DNA.
Translation elongation factor EF-1 alpha/Tu and cadherin had been identified previously, thus ensuring that the procedure described in this work is suitable to the identified proteins bound to DENV and E protein domain III.
The two arches and the three vaults experimentally described in Carozzi et al. (2017) are here analyzed with a novel robust FE lower bound limit analysis code, suitable to predict active failure mechanisms, lines of thrust and collapse loads in absence and presence of TRM, SRG and FRP reinforcement.
With the argument of appropriate size, good covering, and suitable end groups being able to bind an active principle, several tests of biocompatibility were performed on the obtained nanostructures, the first step being that of swelling behavior.
The complete peptide binding problem can be visualized as a three step process: (i) finding a path on the surface of the protein which defines a suitable region for the peptide to bind, (ii) finding the appropriate peptide for this path, and (iii) improving the peptide for a more stable binding required for inhibition.
Among the known ER chaperones, endoplasmin (grp94) possesses the ability to bind peptides suitable for assembly on to MHC class I molecules together with calreticulin [ 51].
The first step was to bind a suitable silane to fibres, in this case 3-chloropropyl trimethoxysilane 3-chloropropyl trimethoxysilanesurface of the finres the cordertong arm of suintroducength and the –Cl functionto group.
13 To test if this system is suitable to deliver other HIV antigens such as cationic Tat, his-Tat was bound to the surface of Ni-NPs.
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