The gene-transfected DO-11.10 cells and silk solutions from W1, S01, S13, and S15 strains were processed for immunoblot analyses according as described previously14 (link). After blocking with Blocking One (Nacalai Tesque, Kyoto, Japan) for 1 h at room temperature and incubated with anti-Myc polyclonal antibody (MBL, code no. 562, Nagoya, Japan), anti-β-actin rabbit MAb (Cell Signaling Technology, code no. #4970, Danvers, MA, USA), and anti-FibL polyclonal antibody14 (link), followed by horseradish peroxidase conjugated anti-rabbit immunoglobulins (Igs) (Dako, code no. P0399, Glostrup, Denmark), and imaged with Chemi-Lumi One L (Nacalai Tesque).
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