Endy:Restriction Digest

From OpenWetWare
Revision as of 20:33, 14 July 2005 by Reshma P. Shetty (talk | contribs)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to navigationJump to search
The printable version is no longer supported and may have rendering errors. Please update your browser bookmarks and please use the default browser print function instead.

Materials

  • Need roughly 3-5 μL of prepped DNA. Aim for 1 μg of DNA.
  • Restriction buffers
    • EX – EcoR I & BSA
    • ES – EcoR I
    • XP – 3 & BSA
    • SP – 2 & BSA
    • ddH2O

Notes for improving efficiency of EcoRI/SpeI Double Digest

Digest Mix

  • μg DNA from prep or PCR
  • 10% (by volume) Restriction Buffer
  • 1% (by volume) BSA stock
  • 2.5% - 5% (by volume) of each restriction enzyme.
  • ddH2O to produce correct percentages by volume

Enzymes < 10% of total volume so glycerol is < 5% of total volume. At higher glycerol concentrations, star activity is sometimes observed (meaning that the enzyme cuts at places other than its recognition site).

Example - 20μl mix

  • 2.0 μL Restriction Buffer
  • 0.2 μL BSA stock
  • 3-5 μL DNA from prep or PCR
  • 0.5 μL Restriction Enzyme Stock
  • X μL ddH2O (to bring solution up 20μL)

Incubate reaction at 37°C overnight (minimum 4-6 hours).

Store at -20°C.