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This was further corroborated well by interaction of 1 and 2 with 5′-GMP.
Moreover, upon interaction of 1 + F− with CO2 the original chromo and fluorogenic behavior of the probe was revived.
Binding of complex 1 with CT DNA was investigated by using vivid spectroscopic techniques to study the mode of the interaction of 1 towards CT DNA.
The absorbance and fluorescent intensities of 1 increased linearly in aqueous solution upon the interaction of 1 with Al3+ or Fe3+.
Interaction of 1 and 3 with CT DNA was carried out by optical methods to ascertain the mode of binding, mechanism of action and their therapeutic potential.
Likewise, the interaction of 1 with human serum album (HSA) revealed the change in intrinsic fluorescence intensity of HSA and was supposed to be associated with the microenvironment of Trp residue.
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Sharma, K. K., Kaur, H., Kumar, G. S. & Kester, K. Interaction of 1,1′-bi 4-anilino)naphthalene-5,5′-disulfonic acid with alpha-crystallin.
Interaction of 1- 4-morpholinophenyl)ethanone 1- 4-morpholinophenylitrile or ethyl cyanoacetate 2 afforded Knoevenagel–Cope product 3.
Interaction of 1,7-dithia-4,11-diazacyclotetradecane (1) with nickel II), copper II) and silver(I) yields the complexes [NiL(H2O)(CH3CN)](ClO4 2, [CuL](ClO4 2 and [AgL]n(ClO4 n (L = 1).
To evaluate the biological preference of chiral drugs for inherently chiral target DNA, interaction of 1 3 with calf thymus DNA in Tris HCl buffer was studied by various biophysical techniques which reveal that all these complexes bind to CT DNA non-covalently via electrostatic interaction.
Polyamines also affect photosynthetic oxygen evolution and therefore, this study was designed to investigate the interaction of 1,3-diaminopropane, 1,4-diaminobutane (putrescine), and 1,5-diaminopentane (cadaverine) cations with proteins of photosystem II (PSII) using PSII-enriched submembrane fractions with diamine concentrations between 0.01 and 20 mM.
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