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Both assays proved the stability of the compounds with respect to hydrolysis and trans-complexation.
The assays proved to be highly specific with no cross amplification.
Systematic evaluation of anticoagulation, including in vitro platelet adhesion assays and hemolytic assays, proved that COOH+/graphene has significant anticoagulation.
GUS assays proved that the isolated promoter was able to direct the expression of the reporter gene in transgenic tobacco.
Conclusion: The presented approach to generate competitive internal controls for use in LightCycler PCR assays proved convenient und rapid.
The results obtained in terms of cell morphology (phase contrast microscopy) and cytotoxicity (LDH and MTT assays) proved biocompatibility.
Similar(23)
Site-directed mutagenesis and functional assays prove the involvement of the Zn and flexible loop in catalysis.
However, in-vitro cell-based assays prove extremely useful for the characterization of immunoassay-positive samples to determine if the detected antibodies have neutralizing properties.
Nuclear run-off assays prove the repression of the GUS transgene expression was due to post-transcriptional silencing (PGTS) [ 25].
The attribute of L-cells to differentiate into three mesodermal lineages (osteogenic, adipogenic, and chondrogenic) in in vitro clonal assays proves the trilineage potential of this cell fraction.
The assay proved to be highly sensitive and capable of detecting picograms of S. pseudotuberosa DNA.
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