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Cells were fixed and permeabilized with cold (−20°C) methanol immediately before being processed for immunofluorescence.
Coverslips were blocked in PBS containing 20% goat serum (GS) for 30 min at 37°C, before being processed for immunofluorescence.
Cells were fixed and permeabilized with 4% paraformaldehyde/0.1% Triton X-100 for 10 minutes at 4°C immediately before being processed for immunofluorescence.
Cultures were fixed with 4% paraformaldehyde in 4% sucrose-containing PBS 18 h after transfection before being processed for immunofluorescence.
The time required to complete the irradiation pattern was approximately 8 min. Cells were allowed to recover at 37°C for 30 min before being processed for immunofluorescence.
After 24 h of treatment, the culture medium was replaced by DMEM/F-12 medium supplemented with 0.5% FBS, and cells were kept for additional 48 h until being processed for immunofluorescence and gene knockdown analysis.
Similar(53)
Samples were processed for immunofluorescence microscopy using standard procedures.
Cells were processed for immunofluorescence after 24 hrs.
Cells were processed for immunofluorescence as previously described [50].
Sections were processed for immunofluorescence as described below.
Tissue sections were processed for immunofluorescence as described previously [17] [17].
More suggestions(15)
being processed for immunoblotting
being processed for immunohystochemistry
being processed for food
being processed for storage
being processed for microarray
being processed for isolation
being processed for release
being processed for treatment
being processed for multicore
being processed for flow
being processed for delivery
being processed for seed
being processed for immunocytochemistry
being processed for capillary
being processed for hire
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