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Ethanol tolerance test was used in order to assay the ability of the 102 mutations that harboring SPT15 genes.
In the in vitro cytokine release assay, the ability of GPC3 CAR-T cells to secrete cytokines has been evaluated.
We used N2 and H2 plasma to treat polystyrene surface and we evaluated, using crystal violet assay, the ability of bacteria possessing hydrophobic or hydrophilic surfaces to adhere on the polymer, at distinct periods of shelf life.
In vitro chaperone-like assays were used to assay the ability of α-crystallins to protect client proteins from chemical or heat induced aggregation.
The enormous advantage an mRNA diagnostic would enjoy over protein is that unlike the lengthy optimization required for each protein assay, the ability to detect newly discovered mRNA sequences is as easy as synthesizing complementary probes.
In this assay, the ability of the investigated H. perforatum fractions to act as donors of hydrogen atoms or electrons in transformation of DPPH radical into its reduced form DPPH-H was investigated.
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We assayed the ability of co-transformant L 61 to degrade lignin using wood meal derived from Japanese cedar.
While there are many pathogen-specific diagnostic assays, the ability to test for large numbers of pathogens simultaneously is lacking.
We assayed the ability of each defensin to downmodulate CD4, CCR5 and CXCR4.
Subsequently, we assayed the ability of the different SUB gSUBmut:EGFP reporters to rescue the sub-1 phenotype.
Therefore we assayed the ability of Treg or TregKIF to bind to ligands of CD62L, VLA-4, and LFA-1 in an in vitro adherence assay (Fig 4a).
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