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The large size of fibrinogen (340 kDa) and polymerized fibrin necessitates digestion prior to gel electrophoresis. Protein samples were digested with 9 M urea containing 9% ¦Â-mercaptoethanol and 3% SDS (50 ¦ÌL) overnight at RT. Each sample (10 ¦ÌL) was separated using a 3 −8% Tris-acetate gel (Invitrogen) and proteins were stained with Coomassie Blue R-250.Gels were imaged using a Typhoon 9210 variable mode scanner (Amerisham Biosciences) and analyzed using ImageJ.ÆäÖеÄProtein samples were digested with 9 M urea containing 9% ¦Â-mercaptoethanol and 3% SDS (50 ¦ÌL) overnight at RT. ÊÇʲôÒâ˼£¬ÈÜÒº¸ÃÔõôÅäÖÆ£¿ |
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Protein samples were digested with 9 M urea containing 9% ¦Â-mercaptoethanol and 3% SDS (50 ¦ÌL) overnight at RT ÖÐÎÄÒâ˼ÊÇ£ºÊÒÎÂÏÂÓÃ50¦ÌlµÄ'9 M urea containing 9% ¦Â-mercaptoethanol and 3% SDS'ÈÜÒº¹ýÒ¹´¦Àí¸Ãµ°°×ÑùÆ· ÖÁÓÚ¸ÃÈÜÒºÔõôÅäÖÆ£¬È˼Ҳ»ÊǸæËßÄã³É·ÖºÍº¬Á¿ÁËô |

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