The phrase "assays we evaluate the" is not correct in written English as it appears to be incomplete or improperly structured.
It could be used in a context where you are discussing the evaluation of assays, but it needs to be rephrased for clarity.
Example: "In our research, we focus on the assays we evaluate to determine their effectiveness."
Alternatives: "the assays we assess" or "the assays we analyze".
To exclude TIS-T cells as a potential source of cytokines in the CC assays, we evaluated the identity of the cytokine producing cells by flow cytometry.
After establishing the antiangiogenic efficacy of MLN4924 in multiple classical assays, we evaluated the efficacy of MLN4924 on in vivo tumor angiogenesis and growth.
Using specific immunoradiometric assays, we evaluated the clinical usefulness of chromogranin A and the α-subunit of glycoprotein hormones in neuroendocrine tumours of neuroectodermic origin.
Using ELISPOT assays, we evaluated the T-cell reactivity for all the mutants and found that immunization with either of them induced IL-4 as well as IFN-γ-secreting T cells (Fig. 4C).
Through combinatory chemistry assays, we evaluated the superoxide (O2●—), hydroxyl radical (OH●), hydrogen peroxide (H2O2) and peroxynitrite (ONOO—) scavenging capacity of jacareubin (xanthone III) and 2- 3,3-dimethylallyl -1,3,5,6-tetrahydroxyxanthone (xanthone V).
In our dose finding assays, we evaluated the impact of a wide dosing range (1, 3, 6, 12, 24 and 48 mg/ml) of lamotrigine on fly mortality (data not shown).
Prompted by the findings of mir-660 downregulation in lung cancer patient tissues and plasma and by the antitumoral effects observed after mir-660 overexpression in in vitro assays, we evaluated the potential role of this miRNA in the inhibition of tumor growth in immunodeficient mice.
Using an in vitro LINE-1 retrotransposition reporter assay, we evaluated the abilities of several antiretroviral compounds to inhibit LINE-1 retrotransposition.
Using this assay, we evaluated the effects of hlyA on larval development and found that all L1 worms that were fed on the hlyA-deficient V. cholerae strain HNC45 reached L4 stage and beyond at 48 hours (Fig. 2B).
Prior to performing the cell-based assay, we evaluated the toxicity of the MC and MC lysate in RBL SX-38 cells.
