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Recipient mice were sacrificed at 3 weeks after cell transplantation and their eyes treated for analysis.
Patients documented alive ≥ 6 months after transfer were treated for analysis as alive at relevant study year-end.
Amplicons were treated for analysis restriction of amplified fragments (ARDRA) with 10 U of enzymes MboI and BamHI (New England, Bio-Lab UK).
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The suspension of activated sludge was treated for the analysis of As to analyze the mechanism of As removal, and the treatment method of the suspension of activated sludge was described as follow.
Subsequently, cells were fixed and treated for immunofluorescence analysis.
After that, cells were cultured in DM either for 1 h at 4°C, or at 37°C for 20, 40, 60 and 150 min. Finally, cells were fixed and treated for immunofluorescence analysis with monoclonal anti-PLP antibody and streptavidin-Alexa Fluor 555 (Invitrogen) to visualize biotinylated proteins.
Cells were treated for biochemical analysis or processed for fluorescence microscopy 72 h after transfection.
GSE10846 was split according to treatment groups (CHOP [cyclophosphamide, doxorubicin hydrochloride (hydroxydaunomycin), vincristine sulfate (Oncovin), prednisone]/R-CHOP [rituximab-CHOP]), which were treated independently for analysis, thus giving a total of 11 data sets.
With exception of 25D, only measured in serum samples of animals treated for seven weeks, the analysis was performed after both five and seven weeks of treatment.
Similar association between optic disc image analysis and low PP was also found in subjects treated for systemic hypertension by subgroup analysis [ 51].
Stability analysis is treated for each type of resonance.
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CEO of Professional Science Editing for Scientists @ prosciediting.com