CleanSweep DNA Clean-up Kit (E686) For removing linkers and primers from enzymatic reactions

Directions for Use


System Components:

CS-1 5 mg **/10 labels

CS-2 1 ml

CS-3 10 ml

CS-4 25 ml

** Upon arrival, CS-1 should be reconstituted in 1 ml sterile dH2O, separated into aliquots and labeled (labels provided) before storing at -20°C.

 

Storage:

CS-1 Frozen

CS-2 Room Temperature

CS-3 Room Temperature

CS-4 Room Temperature

 

INSTRUCTIONS:
Step 1: Following enzymatic reaction, adjust the volume of the reaction solution to 100 L with dH2O.
Step 2: Add 5 L of CS-1, 10 L of CS-2 and 60 L of CS-3. Vortex to mix. Centrifuge at high speed in a microcentrifuge at room temperature  for 5 minutes.

* For small linkers (< 30bp), step 3-5 may be eliminated *

Step 3: Discard the supernatant.
Step 4: To the pellet, add 100 L of H2O. Vortex to dissolve pellet.
Step 5: Add 60 L of CS-4. Vortex to mix. Centrifuge at high speed in a microcentrifuge at room temperature for 4 minutes.
Step 6: Carefully remove the supernatant and add to the pellet 200 l of CS-5.

                Vortex to mix. Centrifuge at high speed in a microcentrifuge at room temperature for 1 minute. Remove the supernatant and dry  the pellet under vacuum.

Step 7: The sample can now be dissolved in the desired volume of dH2O or TE.

For Hazards & Additional Information see MSDS.

 

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