Melbourne/Diagnostic Digest
From 2007.igem.org
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====Method from primary and secondary reagents==== | ====Method from primary and secondary reagents==== | ||
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| - | *[[Melbourne/primary Restriction enzymes and buffer]] | + | *[[Melbourne/primary Restriction enzymes|Restriction enzymes and buffer]] |
*DNA for digestion | *DNA for digestion | ||
*[[Melbourne/primary milliq|milliQ water]] | *[[Melbourne/primary milliq|milliQ water]] | ||
Revision as of 13:08, 28 September 2007
<Return to list of protocols> <Team home page>
- Applications:
- Identification of insert presence
- Time to complete protocol:
- Lab time: 15min, 15min.
- Waiting time: 1-3hours
- Approximate cost of materials: $0.00
Method from primary and secondary reagents
Primary & secondary Reagents Required including controls
- Restriction enzymes and buffer
- DNA for digestion
- milliQ water
Method including controls
For 20uL reation volume
- Make the following reaction mixture on ice.
- Reaction Mixture
- 0.5uL Enzyme 1
- 0.5uL Enzyme 2
- Add enzymes last only take out of the freezer once ready to add.
- 2uL appropriate 10x buffer (see table on fridge)
- 2uL 10x BSA
- 10uL MilliQ
- 5uL DNA
- If performing the same digest for multiple DNA samples make up mastermix of buffer enzyme soultion and make 15uL aliquots to which to add the DNA.
- Volume DNA may vary depending on concentration, vary water volume to achieve 20uL reaction volume.
- Reaction Mixture
- Incubate for 1-3 hrs at 37 degrees.
- Stop reaction with addition of 5uL 6x DNA loading dye.
- Can be stored at -20 or run on gel immediately.
Equipement Required
- microfuge tubes
- Ice box and ice
- 37 degree incubator
- Pipettes and tips
References
