Cell fractionation
Cell fractionation is the separation of homogeneous sets, usually organelles, from a population of cells.
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[edit] Steps
There are three principal steps involved:
- Disruption (homogenization) of cells and liberation of organelles.
- Macro Filtration
- Purification of cell components.
[edit] Homogenization
Tissue is typically homogenized in an isotonic buffer solution using a variety of mechanisms. A 'Potter-Elvehjem homogeniser' is often used as it is relatively gentle. Other procedures include grinding, mincing, chopping, pressure changes, osmotic shock, freeze-thawing, and ultra-sound homogenization.
The solution is homogenized in an isotonic solution to stop osmotic damage, with a pH buffer to regulate pH, and at an ice-cold temperature to prevent enzyme damage. The organelles are kept either cold, isotonic or buffered.
See Cell disruption for further details.
[edit] Filtration
This step may not be necessary depending on the source of the cells. Animal tissue however is likely to yield connective tissue which must be removed. Commonly, filtration is achieved either by pouring through gauze or with a suction filter and the relevant grade ceramic filter.
[edit] Purification
Invariably achieved by Differential centrifugation - the sequential increase in gravitational force resulting in the sequential separation of organelles according to their density.
[edit] See also
Media for cell separation by density:
[edit] External links
- Microfluidicscorp - MFIC OTC
- Subcellular Fractionation Kit Review from Biocompare
