"quantitative immunofluorescence microscopy" is a correct, usable phrase in written English.
You could use it in a sentence such as this: "By using quantitative immunofluorescence microscopy, we were able to measure the expression levels of specific proteins."
Using quantitative immunofluorescence microscopy analysis, a dose response for γ-H2AX foci have also been reported in mouse skin at 30 minutes, 24 hours, and 7 days after whole-body irradiation with doses of 1 to 10 Gy [25].
Lower panels, the distribution of SOX2 in HCC2935 was determined by quantitative immunofluorescence microscopy.
When cultured alone, trophoblasts expressed low levels of β1 integrin as determined by quantitative immunofluorescence microscopy.
DOI: http://dx.doi.org/10.7554/eLife.06132.006 10.7554/eLiFigure32.007 Figure 1 figure supplement 4. Time course of SOX2 induction by quantitative immunofluorescence microscopy.
For XTT and quantitative immunofluorescence microscopy experiments, 1.0 × 10 cells were transfected in 96-well plates in a final volume of 100 μL using 0.25 μL/well DMRIE-C.
Semi-quantitative immunofluorescence microscopy was employed to evaluate proteoglycan expression, due to its greater resolution (at essentially the single cell level) compared with biochemical procedures based on total cell protein, and in view of substantial technical obstacles to accurate quantification of large proteoglycan core proteins by techniques such as immunoblotting.
For a comparison of data from these cases, we developed a semi-quantitative immunofluorescence microscopy-based strategy for systematic analysis of the AT1 within subdivisions of the substantia nigra with regard to its steady state levels as well as its specific subcellular location in dopamine neurons in nigral tissue sections.
The efficacy of each stable shRNA clone to downregulate endogenous expression of IPS-1, IRF3 or IRF7 in respective clones were measured by either semi-quantitative PCR, immunoblot or Immunofluorescence microscopy.
Immunofluorescence microscopy and quantitative image analysis were performed as described (Daniele et al, 2008; Vicinanza et al, 2011).
Using single-cell -based time-lapse microscopy and quantitative immunofluorescence, we found that GSCs utilize two cell division modes to generate GSCs.
The biological characteristics and changes of human DFCSs under the effect of TDM were studied with scanning electron microscopy, transmission electron microscopy, immunofluorescence microscopy, immunohistochemistry and quantitative real-time PCR.
