Cytokine levels were measured either individually by ELISA (ELISA ready-set-go, eBiosciences), or as multiple cytokine measurements using BD Cytometric Bead Array kit TH1/TH2/TH17 (CBA, BD Biosciences).
Therefore to overcome these limitations it is beneficial to perform either multiple in situ measurements using a variety of analytical techniques or to combine complementary techniques into one experimental setup; an approach, which often yields new insight.
To ensure a maximum reliability, we decided to focus our resources on multiple and reproducible measurements using the positive mode of the MCC-IMS only.
However, our recorded electrograms reproducibly show an initial negative waveform followed by a larger positive one and correlated well with multiple paired APD70 measurements using a MAP electrode.
Multiple repeated measurements used to evaluate the dynamic changes and to specifically direct the mode of coagulation support, has been advocated [ 24, 25].
Generally, due to issues of social desirability phenomenon and over-reporting of PA that has been associated with the IPAQ, 39 40 it may be necessary to start considering the need for multiple measurements when using the IPAQ for evaluating PA, especially in developing African countries.
Here, we review the formation of the lytic IS and describe quantitative imaging-based measurements using multiple microscopy techniques at a single cell level that can be used in conjunction with established population-based assays to provide insight into the important cytotoxic function of CAR cells.
The MDSFR approach utilizes the γ-specific R SF vs. μ′ sd f relationship for measurements using multiple fibers at each investigated wavelength.
However, the accuracy and speed of the procedure are currently limited by the need for co-localized measurements using multiple fiber optic probes with different fiber diameters.
