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It can be calculated by dividing the number of successful transform ants by the amount of DNA used during a transformation procedure.
This is divided by the amount of DNA used in the transformation and expressed as transform ants per microgram of DNA. Transformation efficiencies between 10^6 and 10^9 represent the normal range for competent E. coli cells.
The factors that affect transformation efficiency are the strain of bacteria, the bacterial colony's phase of growth, the composition of the transformation mixture, and the size and state of the foreign DNA.
cold (Subcloning Efficiency)? Transformation efficiency is defined as the number of colony forming units (CFU) which would be produced by transforming 1 kg of plasmid into a given volume of competent cells. The term is somewhat misleading in that 1 AEG of plasmid is rarely actually transformed.
For successful chemical transformation, 50100 SL of competent cells and 110 NG of DNA are recommended. When a ligation mixture is used as the transforming DNA (often 15 All is sufficient), purification prior to chemical transformation is generally not required.
High Efficiency Transformation Protocol Add 1 pg-100 NG of plasmid DNA (1-5 SL) to cells and mix without voting.
Once DNA is added to the cells, electroporating can be carried out immediately. It is not necessary to incubate DNA with cells. The maximum recommended volume of a DNA solution to be added is 2.5 SL.
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