Difference between revisions of "HPP Assembly Procedure"

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(Created page with ''''Edge Assembly''' This assembly uses BsmBI to free up the Half Edge Word in the first and second Half Edges. Ligase drives the reaction toward completion. Equimolar amounts …')
 
 
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'''Edge Assembly'''
 
'''Edge Assembly'''
  
This assembly uses BsmBI to free up the Half Edge Word in the first and second Half Edges.  Ligase drives the reaction toward completion.  Equimolar amounts of first and second Half Edges are used.  Reactions are scaled up 5 fold to provide enough product in 5 ul for use with 10 ng of destination vector.
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This assembly uses BsmBI to free up the Half Edge Word in the first and second Half Edges.  Ligase drives the reaction toward completion.  Equimolar amounts of first and second Half Edges are used.  The Half Edges should be in a vector that has a different antibiotic resistance than the destination vector.  Reactions are scaled up 5 fold to provide enough product in 5 ul for use with 10 ng of destination vector.
  
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To determine the 5X amount for use in this reaction, use this formula:
 
To determine the 5X amount for use in this reaction, use this formula:
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10 ng destination vector x (Half Edge plasmid size/2114 bp destination size) x (6)
 
10 ng destination vector x (Half Edge plasmid size/2114 bp destination size) x (6)
  
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  9 ul dH2O
 
  9 ul dH2O
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  Total 25 ul
 
  Total 25 ul
  
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  50 cycles of 50C for 2 minutes/16C for 3 minutes
 
  50 cycles of 50C for 2 minutes/16C for 3 minutes
 
  80C for 20 minutes
 
  80C for 20 minutes
 
      
 
      
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Use 5ul of this Edge Assembly for Graph Assembly
 
Use 5ul of this Edge Assembly for Graph Assembly
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'''Graph Assembly'''
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This assembly uses BsaI to free up the Gene/Start/Finish Specific Words in the Graph Edges.  Ligase drives the reaction toward completion.  5 ul of each Edge assembly is used.  The destination vector should have an antibiotic resistance that is different from that of the Half Edge plasmids. 
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5 ul Each Edge Assembly (1X Amount)
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6 ul dH2O
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1 ul (10 ng) Destination vector
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1 ul 10X Promega Ligase Buffer
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1 ul 500 mM NaCl
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0.5 ul BsaI
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0.5 ul T4 DNA Ligase
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Total 10 ul + 5 x number of Edges
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50 cycles of 37C for 2 minutes/16C for 3 minutes
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80C for 20 minutes
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Use 10 ul of this Graph Assembly for Transformation

Latest revision as of 16:04, 30 August 2011

Edge Assembly

This assembly uses BsmBI to free up the Half Edge Word in the first and second Half Edges. Ligase drives the reaction toward completion. Equimolar amounts of first and second Half Edges are used. The Half Edges should be in a vector that has a different antibiotic resistance than the destination vector. Reactions are scaled up 5 fold to provide enough product in 5 ul for use with 10 ng of destination vector.


To determine the 5X amount for use in this reaction, use this formula:

10 ng destination vector x (Half Edge plasmid size/2114 bp destination size) x (6)


9 ul dH2O
5 ul First Half Edge (5X Amount)
5 ul Second Half Edge (5X Amount)
2.5 ul 10X Promega Ligase Buffer
2.5 ul 500 mM NaCl
0.5 ul BsmBI
0.5 ul T4 DNA Ligase
Total 25 ul


50 cycles of 50C for 2 minutes/16C for 3 minutes
80C for 20 minutes
   


Use 5ul of this Edge Assembly for Graph Assembly

Graph Assembly

This assembly uses BsaI to free up the Gene/Start/Finish Specific Words in the Graph Edges. Ligase drives the reaction toward completion. 5 ul of each Edge assembly is used. The destination vector should have an antibiotic resistance that is different from that of the Half Edge plasmids.



5 ul Each Edge Assembly (1X Amount)
6 ul dH2O
1 ul (10 ng) Destination vector
1 ul 10X Promega Ligase Buffer
1 ul 500 mM NaCl
0.5 ul BsaI
0.5 ul T4 DNA Ligase
Total 10 ul + 5 x number of Edges


50 cycles of 37C for 2 minutes/16C for 3 minutes
80C for 20 minutes
   


Use 10 ul of this Graph Assembly for Transformation