Exact(60)
Total AO capacity of real samples was measured by the proposed fast, simple and inexpensive MRAP assay as well.
Samples were tested for the mutagenicity and DNA damaging assay as soon as possible.
The CB2 binding affinity assay as well as functional assay was also conducted on these compounds.
Their stability was investigated by a heparin displacement assay as well as by DNAse I assay.
We model the BrU labelling assay as follows.
Functional TcTrx was detected by activity assay as describe below.
Functional ClPDI was detected by activity assay as describe below.
MTT assay as mentioned by [28] was performed.
Viability was assessed by MTT assay as described.
We have used the micronucleus assay as a measure of predominantly lethal chromosome damage.
After treatment, cells were seeded for clonogenic assay as previously described [3, 4].
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