Suggestions(2)
Exact(28)
To develop the assays, she needed two resources not available at Oberlin: specific ovarian cancer cell lines and a flow cytometer to test binding to the cells.
To test binding specificity, sequences that interacted with the miR-181b seed sequence were mutated from GAATGT to CTTACA, and the synthetic PDCD4 3′-UTR mutant fragment was inserted into an equivalent reporter plasmid.
To test binding specificity, the sequences that interact with the seed sequence of miR-19a/b were mutated (from TTGCAC to AACGTG), and the mutant MTUS1 3′-UTR was inserted into an equivalent luciferase reporter plasmid.
An rCR2 ELISA was developed to test binding to immobilized C3d.
To test binding of the peptide 6a-P to proteoglycans, we employed a small heparin-sepharose column for binding studies.
We used the GFP fusion lines to test binding of LHP1 to AGAMOUS (AG) and SEPALATA3 (SEP3), which are well-established PcG and LHP1 targets [14] [16], [23].
Similar(32)
This control tested binding of the HCRT2-SAP to bind to other peptide receptors.
Building on the success of antibody drug conjugates, we developed a fusion protein consisting of a novel anti-CD22 scFv and apoptin and tested binding and therapeutic effects in lymphoma cells.
Next, we tested binding affinity of other constituents of the navel orangeworm sex pheromone.
Therefore, we tested binding of p73α and p73β to p19 and p21 using a yeast two-hybrid approach.
To examine further the pH-dependent binding of CquiOBP1 to MOP, we tested binding at high and low pH by fluorescence using NPN as a fluorescent reporter [27].
Write better and faster with AI suggestions while staying true to your unique style.
Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com