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Exact(10)
In order to generate the similarity networks in the function of the similarity threshold ECFP fingerprints were generated for the molecules with a diameter of 4. Similarity of the molecules was quantified by the Tanimoto-similarity measure.
The concentration of leukocytes, C3 and C4, and of several cytokines and other molecules was quantified (see Text S1).
The number of molecules was quantified by fluorometry (Quant-iT PicoGreen dsDNA assay kit, Invitrogen, Carlsbad, CA).
The number of recovered cDNA molecules was quantified by limiting dilution PCR and compared to the HIV-1 RNA levels of the original plasma samples.
Following inactivation by various treatments, the residual DNase activity was measured by incubation of λ DNA in optimal conditions and the degradation of 73 bp and 153 bp λ DNA target molecules was quantified by qPCR (Table 3).
Nuf2 number of molecules was quantified using Cse4 as a reference.
Similar(50)
In the present study fluorescence patterns from fewer single molecules were quantified due to the more extensive analysis needed for each pattern.
Small molecules were quantified using previously determined calibration curves.
Small molecules were quantified using a previously determined calibration curve.
All the molecules were quantified using enzyme-linked immunosorbent assay (ELISA).
The level of released total aggrecan molecules were quantified using the G1/G2 assay.
More suggestions(15)
sequences was quantified
species was quantified
particles was quantified
medications was quantified
elements was quantified
molecules was prepared
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molecules was investigated
molecules was measured
molecules was developed
molecules was performed
molecules was kept
molecules was studied
molecules were quantified
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