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Using a saturation binding protocol, we found that MTα suppressed the maximum binding without any greater impact on the affinity of the radioligand, indicating a non-competitive mode of inhibition.
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Combined with a tight-binding analysis, we found that some compounds actually have quasi-flat band.
Nevertheless, combined with a tight-binding analysis, we found that some compounds have almost s2 configuration.
We found different binding sites namely catalytic, inhibitory phosphorylation, cyclin binding and CKS-binding site of the CDK2 contributing towards the binding of these compounds.
We found no protocol for communicating updated evacuation guidance to the 911 operators who were receiving calls for help.
Among the most significant categories, we found terms related to nucleotide binding site such as "ADP binding", "adenyl ribonucleotide binding" or "purine ribonucleotide binding".
We found similar binding characteristics for both antibodies.
Overall, we found that the protocol performed sufficiently well to qualify for effectiveness studies.
We found that both protocols significantly reduce SED and binocular depth threshold.
Within the polypyrimidine tracts, we found potential polypyrimidine tract-binding protein PTB-binding sites [ 30].
Furthermore, we found that ATP binding was required to reinitiate processive stepping after the terminal backstep.
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CEO of Professional Science Editing for Scientists @ prosciediting.com