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Using a single-cell based assay, we found that, in HT22 cells or primary neurons transfected with mutant huntingtin, cell toxicity was accompanied by CBP depletion, rather than merely recruitment.
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Through enumeration of target genes by a real-time PCR-based assay, we found that different hydrocarbon-degrading bacteria had different dynamic changes during phytoremediation.
Using a reporter-based assay, we found that ERβ decreased HIF-1α-mediated transcription.
Using a calibrated gramicidin-based assay, we found that these bilayer-modifying effects are sufficient to alter membrane protein function.
Using a quantitative real time PCR-based assay, we found that 28% of samples in our group showed Aurora A gene amplification, a finding which was superior to the result of Zhou's research which showed amplification in 12% of primary breast cancer cell lines [ 22].
In order to assess the quality of luciferase based assay we also computed the Z-factor.
Using a chemically induced mitotic exit assay, we find that PP2A B55α functions downstream of Cdk1 inactivation.
For convenience, we used ATP based assay in the following experiments.
We used a cell cultured based assay system.
We found that the CD modified biochip platform presented a stronger affinity property for VlsE protein in conjugation with >0.000475 μg/mL of antigen immobilization concentration, which was sensitive enough for fluorescence based assay.
We have developed noninvasive and nucleic acid based assays for the prediction of transplant status and outcome (NEJM 2001 and NEJM 2005).
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