Team:Washington/Protocols/Gib Rxn

From 2011.igem.org

(Difference between revisions)
(Created page with "{{Template:Team:Washington/Templates/Top}} =Gibson Cloning/Assembly= # Add 15uL of Gibson MasterMix to each tube. # Add ~20-30 ng of purified Backbone DNA to the reaction tube...")
(→Gibson Cloning Protocol)
 
(4 intermediate revisions not shown)
Line 2: Line 2:
-
=Gibson Cloning/Assembly=
+
__NOTOC__
-
# Add 15uL of Gibson MasterMix to each tube.
+
=Gibson Cloning Protocol=
-
# Add ~20-30 ng of purified Backbone DNA to the reaction tube.  
+
 
-
# Add ~20-30 ng of purified Insert DNA to the reaction tube.
+
 
-
# Fill the remaining tubes with distilled H20 to ensure a final volume of '''20 uL'''
+
==Materials Needed==
-
# After making sure all tubes are appropriately labeled, incubate all samples for ~1 hour @ 50oC.
+
#5X isothermal (ISO) reaction buffer (25% PEG-8000, 500 mM Tris-HCl pH 7.5, 50 mM MgCl2, 50 mM DTT, 1 mM each of the 4 dNTPs, and 5 mM NAD). This is prepared as described below.
 +
#T5 exonuclease (Epicentre)
 +
#Phusion DNA polymerase (New England Biolabs)
 +
#Taq DNA ligase (New England Biolabs)
 +
 
 +
 
 +
==Equipment==
 +
#Heat block or thermocycler with PCR tubes.
 +
 +
 
 +
==Procedure==
 +
#Prepare 5X ISO buffer. Six ml of this buffer can be prepared by combining the following:
 +
##3 ml of 1 M Tris-HCl pH 7.5
 +
##150 μl of 2 M MgCl2
 +
##60 μl of 100 mM dGTP
 +
##60 μl of 100 mM dATP
 +
##60 μl of 100 mM dTTP
 +
##60 μl of 100 mM dCTP
 +
##300 μl of 1 M DTT
 +
##1.5 g PEG-8000
 +
##300 μl of 100 mM NAD
 +
##Add water to 6 ml
 +
##Aliquot 100 μl and store at -20 °C
 +
#Prepare an assembly master mixture. This can be prepared by combining the following:
 +
##320 μl 5X ISO buffer
 +
##0.64 μl of 10 U/ μl T5 exo
 +
##20 μl of 2 U/μl Phusion pol
 +
##160 μl of 40 U/μl Taq lig
 +
##Add water to 1.2 ml
 +
##Aliquot 15 μl and store at -20 °C. This assembly mixture can be stored at -20 °C for at least one year. The enzymes remain active following at least 10 freeze-thaw cycles.
 +
###This is ideal for the assembly of DNA molecules with 20-150 bp overlaps. For DNA molecules overlapping by larger than 150 bp, prepare the assembly mixture by using 3.2 μl of 10 U/ μl T5 exo.
 +
#Thaw a 15 μl assembly mixture aliquot and keep on ice until ready to be used.
 +
#Add 5 μl of DNA to be assembled to the master mixture. The DNA should be in equimolar amounts. Use 10-100 ng of each ~6 kb DNA fragment. For larger DNA segments, increasingly proportionate amounts of DNA should be added (e.g. 250 ng of each 150 kb DNA segment).
 +
#Incubate at 50 °C for 15 to 60 min (60 min is optimal).
 +
#If cloning is desired, electroporate 1 μl of the assembly reaction into 30 μl electrocompetent E. coli.
 +
 
 +
 
 +
 
 +
===Based on Methods described in [http://www.nature.com/nmeth/journal/v6/n5/abs/nmeth.1318.html Enzymatic assembly of DNA molecules up to several hundred kilobases], modified by Rob Egbert===

Latest revision as of 19:55, 13 October 2011



Gibson Cloning Protocol

Materials Needed

  1. 5X isothermal (ISO) reaction buffer (25% PEG-8000, 500 mM Tris-HCl pH 7.5, 50 mM MgCl2, 50 mM DTT, 1 mM each of the 4 dNTPs, and 5 mM NAD). This is prepared as described below.
  2. T5 exonuclease (Epicentre)
  3. Phusion DNA polymerase (New England Biolabs)
  4. Taq DNA ligase (New England Biolabs)


Equipment

  1. Heat block or thermocycler with PCR tubes.


Procedure

  1. Prepare 5X ISO buffer. Six ml of this buffer can be prepared by combining the following:
    1. 3 ml of 1 M Tris-HCl pH 7.5
    2. 150 μl of 2 M MgCl2
    3. 60 μl of 100 mM dGTP
    4. 60 μl of 100 mM dATP
    5. 60 μl of 100 mM dTTP
    6. 60 μl of 100 mM dCTP
    7. 300 μl of 1 M DTT
    8. 1.5 g PEG-8000
    9. 300 μl of 100 mM NAD
    10. Add water to 6 ml
    11. Aliquot 100 μl and store at -20 °C
  2. Prepare an assembly master mixture. This can be prepared by combining the following:
    1. 320 μl 5X ISO buffer
    2. 0.64 μl of 10 U/ μl T5 exo
    3. 20 μl of 2 U/μl Phusion pol
    4. 160 μl of 40 U/μl Taq lig
    5. Add water to 1.2 ml
    6. Aliquot 15 μl and store at -20 °C. This assembly mixture can be stored at -20 °C for at least one year. The enzymes remain active following at least 10 freeze-thaw cycles.
      1. This is ideal for the assembly of DNA molecules with 20-150 bp overlaps. For DNA molecules overlapping by larger than 150 bp, prepare the assembly mixture by using 3.2 μl of 10 U/ μl T5 exo.
  3. Thaw a 15 μl assembly mixture aliquot and keep on ice until ready to be used.
  4. Add 5 μl of DNA to be assembled to the master mixture. The DNA should be in equimolar amounts. Use 10-100 ng of each ~6 kb DNA fragment. For larger DNA segments, increasingly proportionate amounts of DNA should be added (e.g. 250 ng of each 150 kb DNA segment).
  5. Incubate at 50 °C for 15 to 60 min (60 min is optimal).
  6. If cloning is desired, electroporate 1 μl of the assembly reaction into 30 μl electrocompetent E. coli.


Based on Methods described in [http://www.nature.com/nmeth/journal/v6/n5/abs/nmeth.1318.html Enzymatic assembly of DNA molecules up to several hundred kilobases], modified by Rob Egbert

Retrieved from "http://2011.igem.org/Team:Washington/Protocols/Gib_Rxn"