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The characteristics of the proliferating cells were examined by immunofluorescent staining using antibodies against deltaNP63, ABCG2 and Keratin 3/12.
b Macrophages loaded with red fluorescent nanospheres infiltrating the brain metastases detected by immunofluorescent staining using anti-human CD68 antibodies labeled with APEX Pacific Blue fluorochrome.
Nerve fibers in matrigel were detected by immunofluorescent staining using antibodies to nerve marker proteins GAP43 (Abcam, cat # ab12274), neurofilaments 200 (Sigma, cat # 4142), peripherin (Abcam, cat # 4666) and tyrosine hydroxylase (Abcam, cat # 112).
First, to demonstrate the doxycycline-dependent induction of E-selectin expression, ES-Endo cells were incubated with increasing concentrations of doxycycline (0 2000 ng/ml) for 5 hours, and the E-selectin expression level on the plasma membrane was analyzed by immunofluorescent staining using anti-E-selectin antibody.
Increased expression of PCAF in LNCaP cells was further confirmed by immunofluorescent staining using an antibody to PCAF.
Localization of the HA- or GFP-tagged proteins was then determined by immunofluorescent staining using the appropriate antibodies.
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The reactivity of anti-dsDNA antibody was tested by immunofluorescent stain using the Crithidia luciliae test (binding site) with mice sera at a dilution of 1 40 in PBS, as suggested by the manufacturer.
Cytofluorimetric sorting of the isolated SCA-1+ cells was carried out by double immunofluorescent staining, using the following directly labeled antibodies (obtained from Pharmingen, San Diego, CA): PE-SCA-1/Ly-6A/E (clonE13-161.7.7), R-APC-CD45R/B220 (clone RA3-6B2), R-APC-CD4/L3T4 (clone GK 1.5), R-APC-CD8a/Ly-2 53-6.7 53-6.7) and R-APC-CD11b (clone M1/70).
Apoptotic cells were identified by fluorescent double immunofluorescent staining using caspase-3 and terminal deoxyuridine nick-end labelling (TUNEL).
Binding of ApoPep-1 to OA joints was demonstrated by ex vivo imaging and immunofluorescent staining using TUNEL and histone H1 and type II collagen antibodies.
Ceramide was also assessed via immunofluorescent staining using an anti-ceramide antibody.
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by nuclei staining using
by double staining using
by immunofluorescent assay using
by immunofluorescent microcopy using
by neuronal staining using
by immunofluorescent microscopy using
by immunohistological staining using
by immunogold staining using
by nuclear staining using
by differential staining using
by immunohistochemical staining using
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