Sentence examples for linkages after from inspiring English sources

As typical OxyR protein, DrOxyR protein did not form intermolecular disulfide linkages after CHP (organic hydroperoxide) or H2O2 (inorganic hydroperoxide) treatment (data not shown).

To precisely define the involvement of the ribose 2′-OH of mRNA in the cleavage reaction, we repeated the experiments using RNAs modified by 2′-O-methylation at A site codon position 1 (MAO), positions 1 and 2 (MAor), or all three positions (MAO3), containing a 2′-deoxy ribose at position 1 (MAD), or phosphorothioate linkages after positions 1 and 2 (MAP).

mRNAs with the sequence 5′-GGCAAGGAGGUAAAAAUGUAGAAAA-3′ were synthesized with appropriate modifications, phosphorothioate linkages after nt 19 and 20 (MAP), 2′-O-methylation at nt 19 (MAO19, 19 + 20 (MAor), or 19 + 20 + 21 (MAor), or a 2′ deoxy ribose at nt 19 (MAD), while "Trunc Asite" had the sequence 5′-GGCAAGGAGGUAAAA AUG-3′.

Thereafter, the nanocarrier was utilized as the signal-generation tag on capture antibody-coating microplate through classical biotin-avidin linkage after reaction with biotinylated detection antibody.

Cleaving this linkage after the initial folding reaction takes place allows us to determine that the shifts in the retention time is actually due to the folding of the chain and not other behavior that might affect retention time.

Ridley et al. [ 169] reported a method for biotin labeling of biologically active oligogalacturonides using a stable hydrazide linkage after first creating the water-instable hydrazone derivative.

Given the novelty of the linkage, it was determined that the first linkage should be used to demonstrate the feasibility of the linkage after which time the additional data would be linked.

The test of pairwise linkage after the Bonferroni correction showed values higher than the significant value of 0.005, indicating that these loci are not linked and can be used as independent markers.

Aluminum methoxy, −Al OCH3 2, and surface Al O Al linkages formed after O3 pulses were suggested as reaction sites for TMA.

19, 30 The first class of SGLT2 inhibitors with O-glycoside linkages modeled after phlorizin were still susceptible to degradation in vivo.

The correlation between the N-terminal product ion current and the number of constituent monomers contributing to that ion current can be exploited to characterize the linkages quantitatively after empirical calibration.