Peptidase (gelatinase) activity was analyzed through the protocol adapted from Cedrola et al. [ 11].
(c) CYP3A4 and CYP2C9 activities were analyzed by LC-MS/MS.
The relative levels of EZH2 binding activities were analyzed by real-time PCR.
ALT and AST activities were analyzed using commercial kits from Nanjing Jiancheng Bioengineering Institute.
The results of the enzymatic activity obtained in the planning were analyzed through analysis of variance (ANOVA), with the estimated effects and regression coefficients being obtained.
Samples with bacteriocin activity collected after gel filtration chromatography were analyzed through SDS-PAGE (Invitrogen) at 200 V for 0.7 h using the Precision Plus Protein Kaleidoscope ladder (Bio-Rad) as a size standard.
Physico-chemical properties and biocompatibility of scaffolds were analyzed through FT-IR, SEM, DSC, mechanical strength analyzer, antibacterial activity and MTT assay.
This in turn guides the way neuronal activities are analyzed.
The dynamics of the neuronal ensemble activity were analyzed as a trajectory through a state space (neuronal trajectory; Figure 5) (Briggman et al., 2005; Mazor and Laurent, 2005; Harvey et al., 2012).
hypotheses were analyzed through covariance analysis test.
