Before 2003, samples were assayed qualitatively using double-nested PCR to amplify BCRABL.
Cell encapsulation was quantified using a DNA measuring assay and qualitatively verified by SEM and confocal microscopy.
An immunochemical assay further qualitatively indicated that the hybrid nanosheets stimulated the production of osteopontin as typical marker for osteoblast differentiation.
The MINC assay yielded qualitatively similar data, but sensitivity was 1 2 orders of magnitude higher.
We used the Gen-PROBE® Amplified Mycobacterium tuberculosis Direct Test which employs a transcription-mediated amplification and hybridization protection assay to qualitatively detect Mycobacterium tuberculosis complex ribosomal RNA (rRNA).
Finally, although predominantly focused on an in vitro description of motility, we wanted to explore whether motion in a Matrigel assay is qualitatively similar to in vivo ookinete motility.
Because we found no mutants that were normal in odorant assays and specifically defective in water soluble assays, we cannot conclude that the two assays measure qualitatively different senses.
3T3 cells were then seeded on the prepared films and cell viability was assessed quantitatively through cell viability and activity assays and qualitatively by light microscopy.
One question is whether the NH4Ac water soluble and odorant assays measure qualitatively different behaviors or are merely quantitatively different measures of the same behavior.
