We have demonstrated the real-time visualization capability of the system by performing a micro-manipulation process using a vitro-retinal surgical tool and a phantom model.
Creatinine levels were quantitated using a Vitros 5.1 FS chemistry analyzer.
These measurements were made using a chemiluminescence assay for the Ntx using a Vitros ECI analyser (Hanson et al, 1992).
ALT was measured in tail blood using a Vitros DT60 II chemistry system (Johnson&Johnson, Rochester, NY).
All other blood analyses were performed on samples taken in EDTA-coated tubes using a Vitros DT II Chemistry System (Johnson and Johnson Clinical Diagnostics, Inc., Rochester, New York, USA).
ALT, AST and GGT were analysed using a Vitros Fusion chemistry system (Ortho Clinical Diagnostics, High Wycombe, UK) at the Western General Hospital, Edinburgh, UK.
The serum was analyzed for total cholesterol, high-density lipoprotein cholesterol (HDL), triglycerides, CRP, and glucose by using a Vitros 5.1 FS Chemistry system.
In vitro proliferation was assayed using an in vitro fluorescence-based assay.
The recombinant P. knowlesi SSP2 and MSP1 (42 kD) proteins used for in vitro T cell restimulation were generated using an in vitro wheat-germ cell free expression system.
Next, the cytotoxic effects of bio-AgNPs were evaluated using an in vitro model.
The present article characterizes the biodurability of single-walled carbon nanotubes using an in vitro assay simulating the phagolysosome.
