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MTT (3- 4,5-dimethylthiazol-2-Yl -2,5-diphenyltetrazolium bromide) assay is the most commonly used assay to evaluate cell proliferation and viability [21].
Currently, the most widely used assay to evaluate gene status in cases scored as 2+ immunostaining is FISH.
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Functional assay by walking track analysis, histological analysis, and electrophysiological evaluation were the most commonly used assays to evaluate nerve regeneration in this model [35] [37].
First, we used MTT assay to evaluate cell viability after exposure to TD52 or erlotinib at the indicated doses for 48 h.
We used this assay to evaluate cystatin C activity in CSF samples from a total of 69 ALS patients, healthy controls, and disease controls.
In this study, we used this assay to evaluate the association between EGFR expression and trastuzumab response in the North Central Cancer Treatment Group (NCCTG) N9831 trial.
The viability of cells was measured using MTT assay to evaluate the cytotoxicity of ADS-I and its metabolites (M1, M2) in Caco-2 cells prior to transport experiments.
We use this assay to evaluate duplex RNAs and single-stranded silencing RNAs (ss-siRNAs) for allele-selective inhibition of ATN-1 protein expression.
Since B49Mod1 inhibits adhesion-independent cell growth, we used a different assay to evaluate the effect of B49Mod1 in long term cell growth.
First, we used telo-FISH assay to evaluate telomere length.
We used the EGFR IF assay to evaluate EGFR expression on samples from 34 patients with metastatic NSCLC enrolled in a phase II clinical trial3.
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