Library concentration and size were assayed on a 2100 Bioanalyzer (Agilent).
Prior to cluster generation, library concentration and size were assayed using the Agilent DNA1000 kit (Agilent) on a 2100 Bioanalyzer (Agilent).
Balb/cByJ mice were transplanted with 500 or 50 of 410.4 MS-1 cells and, beginning on day +7, were treated with vehicle or RQ-08 for 28 days and tumor incidence and size were assayed.
The particle size was assayed at 12 h intervals by DLS.
The average crystallite size was assayed with the Scherrer equation to be ~ 45 nm for the UC phosphors.
The average insert size was assayed isolating 86 recombinant clones that were grown at 37°C overnight in 1.2 ml LB containing X-gal, IPTG and chloramphenicol with shaking (225 rpm).
The numbers and size of neurospheres were assayed 7 days later.
Prior to cluster generation, concentration and size of libraries were assayed using the Agilent DNA1000 kit.
Lipoplex formulations of suitable size and biocompatibility were assayed for DNA delivery, both qualitatively and quantitatively, using RPE cells and a GFP-encoding plasmid.
The catalytic activities of free lipase and the lipase-NPG biocomposites with a pore size of 35 nm were assayed at varying pH (7.0 to 9.0) at 40°C.
