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Removal of DNA from RNA preparations is particularly beneficial when RNA in a sample is amplified using a method that involves reverse transcription using random primers
 The basic principle of the PCR reaction is to heat the DNA to be copied to >90ºC to denature it
 Students will purify proteins from a mammalian tissue (mouse liver) and will use various fractionation and chromatography techniques to purify three target proteins from the mouse liver extract
The kit is designed to give each student experience on how DNA is isolated by scientists from tiny amounts of samples
MC1061 F- Electrocompetent
Acetate Buffer, pH 5.5 [200mM] size:250ml Removal of DNA from RNA