Several methods have been described for the quantification of [C]DASB regional activity [ 18, 20, 32, 38].
More recently, in order to eliminate all major biases seen with conventional chemical shift-based methods, newer multiecho [ 8, 11, 13, 20] and multi-interference [ 10, 12, 19, 21– 23] methods incorporating spectral modeling of fat have been described for the quantification of proton density fat fraction (PDFF).
Few real time RT-PCR assays have been described for detection and quantification of PPRV in clinical samples using TaqMan chemistry [ 7- 10].
Up until now several assays had been described for HIV-2 quantification [ 15, 34, 39- 42], the majority of them using real-time PCR.
Several molecular methods have been described for the detection and quantification of toxigenic cyanobacteria, however, to date there is no method for the simultaneous detection and quantification of hepatotoxin and neurotoxin producing genera.
First, a calibration procedure is described for experimental quantification of the yield parameters.
Two new methodologies were described for the simultaneous quantification of cetirizine (CTZ), PPA and NMS.
In this paper, a method is described for the stoichiometric quantification of molecules in bio-nanostructures.
In this study, a convenient, sensitive and specific real-time PCR assay was described for the species identification and their quantification in raw and cooked meat products.
Numerous LC-MS/MS methods have been described in literature for identification and quantification of low abundant oxylipins using multiple reaction monitoring (MRM) as an ion selective mode.
