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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.
A good rule to follow is this: if your efficiency is equal to or less than 5 × 107 CFU/kg DNA, use these cells for plasmid transformations. If your efficiency is greater than 5 × 107 (ideally 1 × 108 or higher), use these cells for ligation and other assembly reaction transformations.
The process of gene transfer by transformation does not require a living donor cell but only requires the presence of persistent DNA in the environment. The prerequisite for bacteria to undergo transformation is its ability to take up free, extracellular genetic material. Such bacteria are termed as competent cells.
Most recent answer. When you get at least 100 CFU from a transformation made with 0.1 ng of circular plasmid (ideally pUC18 or pUC19). This level of competency (106 CFU/kg of DNA) is the lower limit required for efficient cloning purpose.
Plasmid or vector transformation is the process by which exogenous DNA is transferred into the host cell. Transformation usually implies uptake of DNA into bacterial, yeast or plant cells, while transfection is a term usually reserved for mammalian cells.
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.
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