Sentence examples for conjugation of the two from inspiring English sources

Chemical conjugation of the two enzymes resulted in molecules with higher antioxidant activity and therapeutic efficacy.

Since conjugation of the two mitogens was required to induce the production of IgG3, it was likely that co-ligation of TLR4 and BCR was sufficient to activate the IgM to IgG3 switching mechanism in the absence of T cells.

This ribose-free sugar was used for the conjugation of the two aminooxy-functionalized RGD peptides c RGDfK) and c RGDfC) [ 36], which were conjugated at room temperature in sodium acetate buffer at pH 4.6.

The structure of Cj-YCC indicated the "western" meso position to be unsaturated, opening up conjugation of the two "western" pyrrole rings, and giving rise to a chromophore related to the one found in bilirubin.

Conjugation of the two drugs to the phage nanoparticles was done by using EDC chemistry, forming an amide bond between the exposed carboxyl side chains on the phage coat, mostly the ones exposed on g8p, and a free primary amine on the drugs.

The conductance of the three molecular wires decreases with an order of planar p-terphenyl > dibenzo[cd, Im]perylene > dibenzo[bc, kl]coronene, which is reverse to the order of the levels of conjugation of the three molecules.

The conjugation of these two effects probably explains the absence of concordance in the single nuclear gene trees (not show), although the same general topology was recovered in the concatenated nuclear phylogeny.

This is correlated to a change in conjugation effect of the two positional isomers of naphthalene in the polymer backbone, where in 1,4-conjugation an aromatic sextet remains intact in one of the naphthalene rings whereas 1,5-conjugation involves the loss of resonance energy in the entire naphthalene unit.

Since the mass spectra of M1 and M2 were identical, it was not possible to distinguish the position of glucuronic acid conjugation in the two isomers.

This attractive TX ability stems from combination of its (i) high conjugation efficiency in each of the two planar moieties, (ii) intrinsic 3D structure on account of the presence of the central node, and (iii) intrinsic regioselectivity in electropolymerisation on account of the positions of the two available free α-thiophene sites.

X-ray single crystal structural analysis shows that the dihedral angles involving the difluorophenylene moiety and two pyridine rings of the 2,2′-bipyridine unit in (2Fphen-bpy)Eu DBM 3 are 42° and 51.6°, indicant of non-conjugation between the two segments.