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Electroporation - Gene Transfer Methods - Electroporation is a gene transfer method in which DNA is transferred into cells by using high voltage current for a fraction of second.

This method can be applied to transfer DNA into plant cells, animal cells, yeast and bacteria. In this method, cells are placed between the electrodes present in an electroporation chamber along with an ionic solution containing the vector DNA.

An electric pulse generated by a capacitor is applied for about 10-45 milliseconds, which induces pores in the plasma membranes.

These pores appear to be round and are present for several minutes after the pulse during which vector DNA passes through the pores into the cell.

The transformation efficiency by this method depends upon the field strength or amount of current applied and the time of application. High voltage (1.5 kV) can be applied for a short duration of 10 milliseconds or a low voltage of 350 V can be applied for a longer duration of 54 milli seconds.

Transformation efficiency can also be increased by using various other methods such as adding 13% PEG solution into the electroporation chamber, linearing the DNA or heat shocking (45°C for 5 min.) prior to impulse.