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Double label experiments provided evidence that α4 and β2 subunits co-localize on small RGCs.
Platelet activation was analysed by double label flow cytometry, using monoclonal antibodies against GP53, P-selectin, and platelet-bound fibrinogen.
Identical results were obtained using double label fluorescent ISH (Fig. 1A C and G I) or double label colorimetric-fluorescent ISH (Fig. 1D F and J L).
Identical results were obtained using double label fluorescent ISH (Fig. 2C H) or double label colorimetric-fluorescent ISH (Fig. 2I N).
Double label immunofluorescence was employed to identify the intensity of phosphorylated CREB (pCREB) in the striatal spiny projection neurons [53].
Double label ISH revealed that TMEM44 signals partially colocalized with SHH signals (Fig. 3L) in cells at the bottom of taste buds.
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O'Neill, J. W. & Bier, E. Double-label in situ hybridization using biotin and digoxigenin-tagged RNA probes.
Double-label immunocytochemistry was used to assess colocalisation of ERβ with the neurohypophysial hormones in male rats.
The data presented here can be used in the design of future studies employing double-label mapping of neural activation following a compound stimulus.
Quantitative analysis of Pc 4 localization in mouse lymphoma (LY-R) cells via double-label confocal fluorescence microscopy.
This study utilizes double-label tryptic peptide comparisons in combination with both conventional and microsequence analyses to investigate the structure of two such variants, M7 and DR1.
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