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2009
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June
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- 2% GA in 0.05M PB, 0.1M Sucrose
- 2.5% GA, 4% PFA in 0.1M CB, 0.1M Sucrose
- 5% Gluteraldehyde in 0.1M Cacodylate Buffer
- 1% OsO4 in buffer
- 2% OsO4 in buffer
- 2% GA, 2% PFA in 0.1M Cacodylate Buffer
- 2% GA, 2% PFA in 0.1M Phosphate Buffer
- Perfustion Fixative II
- Standard processing for IEM
- 3% Paraformaldehyde for IEM
- 0.1M Cacodylate Buffer containing 4% Sucrose and 0...
- 0.1M Cacodylate Buffer containing 4% Sucrose IEM
- Making Urynal Acetate and Lead Citrate
- Postembedding Immunolabeling
- Processing hard to penetrate tissues for standard TEM
- Standard processing for TEM
- Processing Platelets for Standard TEM
- Platelet Resin
- White's Buffer Solution
- Glutaraldehyde in White's Saline
- Muscle Processing for Standard TEM
- 0.18M Phosphate Buffer (muscle)
- Isoosmotic Phosphate Buffer (Muscle)
- 0.1M Tris Wash (Muscle)
- 0.4M Phosphate buffer Stock (Muscle)
- Mouse Glutaraldehyde Fixative (muscle)
- 1% OsO4 in 0.1M PB for Muscle
- Toluidine Blue Stain
- Sodium Phosphate Buffer from Monobasic and Dibasic...
- Processing tissue for Immuno Electron Microscopy
- Heavy Metal Staining for TEM Thin Sections
- Making a loop for grid transfer
- Making Resins
- Sodium Cacodylate Buffer
- Perfusion Fixative I
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June
(35)
Thanks for posting! Is it okay to warm the cacodylate buffer? I'm used to making PFA in PBS...can I use the same procedure (heating the solution to 60C) with CacBuf?
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