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This result appears to correlate with our initial purification method using the assay for synergistic hydrolysis of Avicel.
There was significant inhibition of the recruitment of eosinophils into the lung tissue associated with an exacerbation, assessed using the assay for eosinophil peroxidase activity (P < 0.001)).
Using the assay for intracellular nucleosomes, an acid-pulse alone significantly reduced serum-starvation induced apoptosis by 23% and leptin reduced apoptosis by 36%.
No positive amplification of nucleus-embedded mtDNA sequences was obtained from the cell line using the assay for mtDNA (data not shown).
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Successful reverse transcription was confirmed by the quality check of the cDNA using the assays for the reference genes GAPDH, USO1 and Tmem111.
The outbreaks were first tested using the assays for NoV. Then, all outbreaks that remained negative were further tested using the assays for rotaviruses, adenoviruses, astroviruses and sapoviruses [ 1].
Some laboratories had the Elispot assay established less than one year before panel testing, whereas others used the assay for more than 10 years.
Seven different laboratories carried out this method and used the assay for detection of the carbapenemase genes on a selection of 20 isolates.
The purified enzymes were assayed for residual cis-CaaD activity using the colorimetric assay for dehalogenation (5).
Apoptosis was confirmed using the TUNEL assay for each stimulus.
A similar finding was obtained using the TUNEL assay for apoptosis in cultured podocytes.
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