[55] Polyethylene glycol embedding protocol for immunofluorescence microscopy

[1]  J. Olmsted,et al.  MAP 4: a microtubule-associated protein specific for a subset of tissue microtubules , 1984, The Journal of cell biology.

[2]  J. Olmsted,et al.  MAP 4: occurrence in mouse tissues , 1984, The Journal of cell biology.

[3]  V. Parsegian,et al.  Water near intracellular surfaces , 1984, The Journal of cell biology.

[4]  M. De Brabander,et al.  High resolution light and electron microscopic localization of tubulin with the IGS (immuno gold staining) method. , 1981, Cell biology international reports.

[5]  J. Roth,et al.  Enhancement of structural preservation and immunocytochemical staining in low temperature embedded pancreatic tissue. , 1981, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[6]  J. Wolosewick.  The application of polyethylene glycol (PEG) to electron microscopy , 1980, The Journal of cell biology.

[7]  K. Tokuyasu.  A study of positive staining of ultrathin frozen sections. , 1978, Journal of ultrastructure research.

[8]  J. H. Bryan,et al.  Ultrastructural characterization of the manchette microtubules in the seminiferous epithelium of the mouse. , 1977, The American journal of anatomy.

[9]  S. Singer,et al.  Improved procedures for immunoferritin labeling of ultrathin frozen sections , 1976, The Journal of cell biology.

[10]  H. Blank.  A rapid imbedding technic for histologic sections employing a water soluble wax. , 1949, The Journal of investigative dermatology.

[11]  V. Meininger,et al.  Ultrastructural localization of tubulin and actin in polyethylene glycol‐embedded rat seminiferous epithelium by immunogold staining , 1983, Biology of the cell.