In this study, we applied Edu assays to evaluate the role of mono-ADP-ribosylation of H3R117 in increasing proliferation of LoVo cells, further investigated whether TET1 contributed to depression of proliferation in H3R117A mutant LoVo cells.
We performed ex vivo assays to evaluate the effects of - and -carvone, carvacrol, -carveol, and limonene on CAP characteristics using a modified single sucrose-gap method.
The Biomarkers Shared Resource assists investigators with the design and implementation of molecular and protein assays to evaluate biochemical and inflammatory markers.
The T cell response to HBc VLPs was determined using a number of FACS-based T cell assays to evaluate the induced CD4+ and CD8+ T cells in splenocytes, which were known as two prime T cell subsets.
The colorimetric assays to evaluate the aforementioned enzymes were conducted following the manufacturer's protocol (Quibasa, Bioclin, Brazil).
In light of these limitations and uncertainties, we used all three serological assays to evaluate the humoral response induced by the plant-made H5 VLP vaccine in humans.
Using BrdU incorporation and cell viability assays to measure cell proliferation and annexin assays to evaluate cell apoptosis, we found that neither cyclopamine nor Sulindac produced changes in B0 cells.
To examine whether NAFs, pre-cocultured with MDA-MB-468 cells, increase their capacities to support tumor growth, we performed colony formation assays to evaluate the colony formation promotion abilities of NAF #200N.E1-E4 P.4 compared to NAF #200N.
We established assays to evaluate BMTP-11 in vitro, in vivo, and ex vivo.
Therefore, we performed xenograft formation assays to evaluate the effect of miR-144 overexpression on tumorigenicity.
We performed radio-receptor binding, real-time RT-PCR, multiplexed IHC, and ISH assays to evaluate receptor expression.
