Background: Multiple types of assays allow sensitive detection of virus-specific neutralizing antibodies.
MRM assays allow the simultaneous detection of multiple lipid species using analyte-specific information deduced from their MS/MS fragmentation patterns.
Comparing the two methods, both assays allow rapid identification of A. catenella without time-consuming microscopy when multiple sites need to be considered in routine monitoring.
Intracellular cytokine staining (ICS) assays allow sensitive, quantitative ex vivo assessments of antigen-specific T cells including immunophenotyping of responding cells and measurement of multiple effector functions.
Our quantitative ERK activation assays allowed multiple comparisons between structurally related physiologic estrogens (E1, E2, E3) and an XE class (alkylphenols and BPA), and also allowed us to carefully document the combinatorial effects of XEs (both inhibiting and enhancing estrogenicity) on these physiologic estrogens that are functionally important to different life stages of women and men.
Expression of the mRNAs within this panel can be measured quantitatively by multiple assays [ 35], allowing flexibility of the approach during clinical testing.
Using type-specific quantitative assays allowed isolating the effect of HPV type loads in multiple type infections.
Importantly, when a protein regulates multiple aspects of APP, either directly or indirectly, the combination of GAMAREP, AICDREP, and our in vivo cleavage assays allows us to uncover the relative contributions of these regulatory inputs.
In addition, this type of microarray can easily be subdivided into multiple sub-arrays; e.g., 4 sectors of 2240 electrode features per array, which allows multiple assays on one array and provides significant cost savings.
Syringe infiltration offers the flexibility of introducing multiple transgene constructs into different areas, allowing multiple assays to be performed on a single leaf [ 8].
