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细胞技术

细胞组分和细胞器――细胞骨架

2025-02-26 细胞技术 加入收藏
Fixation and Immunofluorescence of the Cytoskeleton (Mitchison Lab) Recycling
  • Fixation and Immunofluorescence of the Cytoskeleton (Mitchison Lab)   
  • Recycling Tubulin (Mitchison Lab)   
  • Labeling Tubulin and Quantifying Labeling Stoichiometry (Mitchison Lab)   
  • Tubulin Polymerization with GTP/GMPCPP/Taxol (Mitchison Lab)   
  • Preparation of Segmented and Polarity Marked Microtubules (Mitchison Lab)  
  • Microtubule Spindowns for Visual Analysis (Mitchison Lab)   
  • Flow Cell Assays with Microtubules: Motility/Dynamics in Fluorescence and VE-DIC (Mitchison Lab)  
  • Negative Stain Electron Microscopy of Microtubules (Mitchison Lab)   
  • Microtubule Pelleting (Mitchison Lab)   
  • Actin - Chromatography Purification (The Cell Biology and Cytoskeleton Group, HMS)    
  • Actin - Labeling with Pyrene Iodoacetamide (The Cell Biology and Cytoskeleton Group, HMS)    
  • Actin Binding Assay with Rhodamine-Phalloidin (The Cell Biology and Cytoskeleton Group, HMS)    
  • Actin Extraction from Acetone Powder (The Cell Biology and Cytoskeleton Group, HMS)    
  • Actin Preparation - Acetone Powder Method (The Cell Biology and Cytoskeleton Group, HMS)
  • Plasma Gelsolin Preparation (The Cell Biology and Cytoskeleton Group, HMS)
  • Some Buffers for Actin Work (The Cell Biology and Cytoskeleton Group, HMS)    
  • Fixing and Immunostaining Cells (The Cell Biology and Cytoskeleton Group, HMS)   
  • Fixing and Staining Cells for Actin with Fluorescently-Labeled Phalloidin (The Cell Biology and Cytoskeleton Group, HMS)
  • "Cells on Gels" (The Cell Biology and Cytoskeleton Group, HMS) this protocol describes method for culture cell on a thin polyacrylamide-based, collagen-coated flexible substrate. By maintaining a constant total concentration of acrylamide while usr/localying the concentration of bis-acrylamide, it's able to obtain a series of chemically identical substrates with a wide range of flexibility. By using imaging techniques,  cells' response to differences in substrate flexibility can be detected.    
  • Immunofluorescent Localization of Tubulin (William H. Heidcamp) For cultured cell   
  • Isolation of Microtubules (Bovine Brain) (William H. Heidcamp)   
  • Viscosity & Polymerization of Microtubules (William H. Heidcamp)    
  • TEM Visualization of Microtubules (William H. Heidcamp)    
  • SDS Gel Electrophoresis of Tubulin\MAPs (William H. Heidcamp)   
  • Isolation of Actin and Myosin Filaments (William H. Heidcamp)    
  • Yeast Actin Capture Assay (D. Amberg)


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