Vaccine constructs (pVR-DMV-F and pVR-DMV-H) were evaluated for expression in vitro and then for immunogenicity in mice.
A cDNA library constructed from C. papaya roots was screened using three different methods, and isolated clones were evaluated for expression in roots, leaves, hypocotyls, flowers, and fruit.
In this study, nine candidate reference genes including TUBA, EF1, EF2, UBC, UFD, RPS5, RPS24, ACTB and 18S were evaluated for expression stability in a diverse set of six samples representing different growth periods.
The myotube cultures were evaluated for expression of the intrafusal fiber-specific alpha cardiac-like myosin heavy chain and for the expression of the non-specific slow myosin heavy chain.
Members of the miR-17 family were evaluated for expression in a vulvar tumor cell line (SW954) and 20 HPV negative formalin-fixed paraffin-embedded (FFPE) samples by quantitative real-time PCR (qRT-PCR).
GFP positive cells were evaluated for expression of the surface proteins indicated.
Bone marrow and Wharton's jelly derived MSCs were evaluated for expression of immunologically relevant ligands upon treatment with IFNγ and TNFα.
Twenty-one cellular loci were evaluated for expression patterns consistent with the allele effects.
Clones were evaluated for expression of tTA using a luciferase assay (see below).
T cells were evaluated for expression of IFN-γ, TNF-α, or IL-2 and for mobilization of CD107a after stimulation with CMV peptide pools.
