Sentence examples for both peptides were able from inspiring English sources

Carboxyfluorescein release experiments with LUVs showed that both peptides were able to permeabilize vesicles although the leakage response to increases in peptide concentration differed.

Furthermore, our results revealed that while both peptides were able to visualise experimental inflammation by PET imaging, 68Ga-DOTAVAP-PEG-P1 showed a higher inflammation-to-muscle ratio than the original 68Ga-DOTAVAP-P1.

Furthermore, our results revealed that while both peptides were able to detect experimental inflammation by PET imaging, 68Ga-DOTAVAP-PEG-P1 showed a higher inflammation-to-muscle ratio than the original 68Ga-DOTAVAP-P1.

Both peptides were able to reduce leukocyte migration, TNF-α levels and microorganism load in the peritoneal cavity after induction of experimental sepsis, decreasing inflammation in the lung and cecum of septic animals.

For BHK-21 DRMs, both peptides were able to induce agreggation.

In the case of PC∶PE∶SPM∶Cho vesicles (Fig. 5C), both peptides were able to shift a small population of the initial vesicles into an aggregate form, indicating that the binding efficiency was not enough to lead into aggregation, as is also shown by FTIR (Fig. 5C).

In our study, molecular docking of OT and OT-GKR showed that while both peptides are able to interact with OTR with significant binding energies, the binding pocket for OT-GKR might be slightly different from the binding pocket for OT.

Our in silico studies showed that both the peptides were able to dock to the monomeric helical state of hIAPP (ESI †).

Since both Bad and Noxa BH3 peptides were able to restore Bim BH3 peptide-induced MOMP in 2LMP mitochondria moderately protected by Mcl-1, the functional assay established under such concentration of recombinant protein would fail to demonstrate the selectivity and specificity of either Bcl-2 or Mcl-1 antagonists.

In fact selected synthetic peptides were able to inhibit the toxin's action in vivo.

These results indicated that the target peptides were able to be quantified in a wide range without the interference from background peptides.