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The assay proved to be highly sensitive and capable of detecting picograms of S. pseudotuberosa DNA.
The assay proved to be specific when different pestivirus strains from swine and ruminants were evaluated.
The antigenemia assay proved unsuitable for the surveillance of hematological transplant patients.
Conclusions: This molecular assay proved to be suitable for routine detection of TTV in clinical samples.
The assay proved to be suitable for the high-throughput routine diagnostic laboratory.
The results of LDH release assay proved that compound 21 was anti-proliferative rather than cytotoxicity on HepG2 cells.
The sensitivity of the assay proved to be 104 and 103 genomic equivalents for positive and negative sense RNAs, respectively.
The 3- 4,5-dimethylthiazol-2-Y -2,5-diphenyltetrazolium bromide (MTT) assay proved FGO as a biocompatible material.
The developed multiplex PCR assay proved to be specific, sensitive down to 30 pg DNA per reaction, reproducible and economical.
Relaxation assay proved that the analogs of the natural product are potent inhibitor against Top2, with stronger activity than the well-known Top2α inhibitor etoposide [43].
Over-expression, knockdown and competitive inhibition of PDX-1 expression assay proved that PDX-1 is a critical transcript factor to regulate the activity of SHIP1.
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