1
Specific cell types that expressed Mincle were detected with double immunofluorescence staining.
2
Differential protein expression patterns were validated by immunofluorescence staining and immunoblotting.
3
Double- immunofluorescence staining found that tumor-associated mouse endothelial cells also expressed pEGFR and pVEGFR.
4
The spatial distribution of hypoxia and immune markers was examined using multiplex immunofluorescence staining.
5
The localization of O-GlcNAc-modified proteins in the retinal vasculature was confirmed by immunofluorescence staining.
6
Finally immunofluorescence staining permitted to evaluate the complete biosynthesis of all the molecules investigated.
7
They presented a smooth rim-like nuclear immunofluorescence staining pattern.
8
Systemic examinations by immunofluorescence staining showed that gp70 was mainly localized in various lymphoid tissues.
9
Nuclear translocation of p65 was detected by immunofluorescence staining.
10
To explore the components of the fiber, we performed immunofluorescence staining of the stretched chromosome.
11
Immunohistochemistry and immunofluorescence staining was used to detect the protein expression in rat carotid arteries.
12
H&E and immunofluorescence staining were used to validate results obtained from the in vivo imaging studies.
13
We then used immunofluorescence staining and western blot to test the transduction efficiency of this vector.
14
Thereafter, we used immunofluorescence staining and western blot to test the transduction efficiency of this vector.
15
Morphologic and molecular changes characteristic of EMT were determined by immunofluorescence staining and Western blot analyses.
16
Double immunofluorescence staining demonstrated that lymphocytes expressing BLV antigens bore B-cell but not T-cell surface markers.
