Back to Home
Home >> Gene Transfer Methods >>Microinjection - Gene Transfer Methods
Back to Home

Microinjection - Gene Transfer Methods - The technique of microinjection is based on the use of glass micropipettes with a 0.5-10 mm diameter tip to directly transfer macromolecules (vectors) into the cytoplasm or nucleus of a recipient cell which is held by a glass suction pipette.

This method is widely used for animal and plant cells.

In this method the recipient cell is held with a suction pipette by using suction pressure.

Micropipette filled with DNA solution or vector DNA is brought to the recipient cell.

Then an appropriate amount of DNA solution is injected into the recipient cell by applying pressure exerted by syringes or mechanized machines connected to the micropipette.

The whole procedure is carried out viewing under an inverted microscope. If large numbers of cells have to be transformed then recipient cells are immobilized on a coverslip with poly L-Lysine or embedded in a thin layer of agarose in a grid pattern.

Two great advantages of this method are the ability to transform the cell with high frequency especially when small numbers of recipient cells are available, e.g. egg, and non requirement of pre treatment procedure for injection.

The only disadvantage with this method is that it is very cumbersome and requires expensive highly skilled personnel.