聚丙烯酰胺凝胶电泳
溶解
色谱法
污渍
特里斯
裂解缓冲液
化学
凝胶电泳
布拉德福德蛋白质测定
蛋白质纯化
十二烷基硫酸钠
分子量大小标记
蛋白质凝胶电泳
膜蛋白
聚丙烯酰胺
膜
分子生物学
生物化学
生物
酶
基因
作者
Dušan Garić,Daciana Catalina Dumut,Amanda Centorame,Danuta Radzioch
摘要
Abstract Western blotting is a method widely used in cell and molecular biology for the specific detection of proteins in biological samples. It is time‐consuming and normally takes up to 2 days to complete. This protocol introduces a more time‐efficient method to complete western blots, covering the preparation of protein extracts (including strategies for solubilization), electrophoretic separation of proteins, transfer of proteins to the membrane, and probing with antibodies. We describe an SDS‐PAGE protocol that achieves a gradient‐like separation of proteins (10‐400 kDa) on a single‐percentage polyacrylamide gel in only 45 min. Additionally, we present a rapid (10‐14 min) semi‐dry transfer of proteins from standard Tris/glycine polyacrylamide gels onto a membrane using homemade Tris/HEPES‐ or Tris/EPPS‐based buffers. © 2023 Wiley Periodicals LLC. Basic Protocol 1 : Sodium dodecyl sulfate–polyacrylamide gel electrophoresis (SDS‐PAGE) Support Protocol 1 : Cell lysis and protein extraction Support Protocol 2 : Protein quantification with BCA assay and sample preparation for loading on gel Basic Protocol 2 : Protein transfer with a fast semi‐dry transfer (FSDT) buffer Basic Protocol 3 : Immunoprobing, chemiluminescent visualization, stripping, and reuse of membranes
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