Team:SDU-Denmark/Protocols/Ligations

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(Protocol 1)
 
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[[Team:SDU-Denmark|Home]] | [[Team:SDU-Denmark/Background|Background]] | [[Team:SDU-Denmark/Project|Project]] | [[Team:SDU-Denmark/Parts|Parts]] | [[Team:SDU-Denmark/Team|Team]]
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[[Team:SDU-Denmark/Diary|Diary]] | [[Team:SDU-Denmark/Protocols|Protocols]] | [[Team:SDU-Denmark/Downloads|Downloads]] | [[Team:SDU-Denmark/Brainstorm|Brainstorm]]
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=Ligations=
=Ligations=
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==Protocol 1==
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=Protocol 1=
Mix the following:
Mix the following:
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Use for electroporation.
Use for electroporation.
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=Protocol 2=
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Takes place in eppendorf tube.
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#2 ul 10x T4 ligase buffer
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#1 ul T4 ligase
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#5 ul PCR product (cut) of each brick which is to be ligated together - or 1 part plasmid and 5 part bricks
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Leave at 17 degrees over-night.
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Test ligation using PCR and run a test gel afterwards in order to check the PCR product has the right size.

Latest revision as of 10:11, 17 August 2009

Home | Background | Project | Parts | Team

Diary | Protocols | Downloads | Brainstorm

Ligations

Protocol 1

Mix the following:

  1. 2uL 10x Ligase buffer
  2. 1uL T4 DNA ligase
  3. 2 or 4 uL cut backbone
  4. 5 or 10 uL cut PCR product

Leave at 17 degress C overnight.

Use for electroporation.


Protocol 2

Takes place in eppendorf tube.

  1. 2 ul 10x T4 ligase buffer
  2. 1 ul T4 ligase
  3. 5 ul PCR product (cut) of each brick which is to be ligated together - or 1 part plasmid and 5 part bricks

Leave at 17 degrees over-night.

Test ligation using PCR and run a test gel afterwards in order to check the PCR product has the right size.