The phrase "assay to explore the" is correct and usable in written English.
It can be used in contexts related to scientific research or analysis, particularly when discussing the examination or testing of something to gain insights.
Example: "The researchers conducted an assay to explore the potential effects of the new drug on cancer cells."
Alternatives: "test to investigate the" or "examine to understand the".
We employed the fluorescence recovery after photobleaching (FRAP) assay to explore the impact of LDs on membrane fluidity of lysosomal-like liposomes.
Here, we use a new kind of wound healing assay, called a sticker assay, to explore the role of initial wound shape.
To assess the possibility that Pias3 employs Trim32 as its ubiquitin E3 ligase, we firstly utilized a GST pull-down assay to explore the potential association between Pias3 and Trim32.
In order to confirm the observation that inhibition of DNA-PK decreased rAAV replication in cells, we employed a previously developed in vitro replication assay to explore the role of DNA-PK and Ku70/80 [43], [43].
In conjunction with biochemical and histological analyses, we have used the CGN assay to explore the properties of Sho.
We also employed differential centrifugation assay to explore the possibility of aggregation of 519Q-SupC and 582Q-SupC fusions that exhibited non-sense suppression phenotype in sup35∆ haploids.
We also employed electrophysiological assays to explore the potential for acute post-translational modification of ion channels during patch clamp experiments.
Considering the data from our previous studies [15], [16] and the current transcriptomic analysis, we conducted further biochemical assays to explore the upregulation of two specific genes that may be associated with the establishment of extracellular matrix and acid production by S. mutans within biofilms: lytT (SMU.576) and glg (SMU.1564).
The luciferase assay is one of the most convenient reporter assays to explore the regulation of gene expression in mammalian cell culture.
We used in vitro and in vivo assays to explore the role of miR-21 in the malignant progression of human breast cancer, using miR-21 knockdown.
In conclusion, we utilized novel high-resolution imaging and single particle tracking microscopy coupled with biochemical assays to explore the spatial organization of TGFβ signaling at the receptor level.
