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For vWF, results are expressed as a percentage of a normal pooled plasma control reference that has been assayed against a secondary standard of the 5th International Standard of vWF [ 20].
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The compounds displayed weak inhibition activity on chitin synthase and their antifungal potencies have been assayed against a large variety of pathogenic fungi.
Liposomes bearing cell-specific recognition ligands on their surfaces have been widely considered as drug carriers in therapy [18, 19], and liposome encapsulation has been assayed for the targeted delivery of compounds against murine malaria [20 22].
Three types of extracts of each garlic and ginger including aqueous extract, methanol extract and ethanol extract had been assayed separately against drug resistant Escherichia coli, Pseudomonas aeruginosa, Bacillus subtilis, Staphylococcus aureus, Klebsiella pneumoniae, Shigella sonnei, Staphylococcus epidermidis and Salmonella typhi.
Our methodology tries to address the problem that, for each molecule that could be synthesised and tested, only a small fraction of its activities against different targets have been assayed.
Moreover, according to literature data, pollen extracts have been assayed very rarely for their antimicrobial activity especially against human pathogenic bacteria and fungi.
A known limitation in molecular bioactivity data is that not every compound has been experimentally assayed against all targets, thus the matrix of available molecule-target data is sparse.
Antimycotic activity was assayed against 8 fungi.
EGFR overexpressing UM-SCC-22B cells were assayed against the radiolabeled antibody 125I-Nimotuzumab.
The susceptibility of the P. acnes and S. epidermidis was assayed against Oleo europaeaL.
The hydrolytic activity of the ManKs_4-555 wassayedyed against various mannan polymers as substrates.
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