Team:Warsaw/Calendar-Main/8 October 2008

From 2008.igem.org

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<h3>Preparation of AID</h3>
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<h3>Preparation of BioBricks</h3>
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<h4>Michał K.</h4>
<h4>Michał K.</h4>
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  primers on colonies from plates with transformations <a href=http://partsregistry.org/wiki/index.php?title=Part:pSB1A3>pSB1A3</a>+ AID (annealing temperature - 55&deg;C, 60 s of elongation step). </li>
  primers on colonies from plates with transformations <a href=http://partsregistry.org/wiki/index.php?title=Part:pSB1A3>pSB1A3</a>+ AID (annealing temperature - 55&deg;C, 60 s of elongation step). </li>
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<li>Inoculation of confirmed colonies to liquid LB + ampicillin. </li>
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<li>Inoculation of confirmed colonies to liquid LB + ampicillin. </li></ol>
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<h3>Preparation of BioBricks</h3>
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<h4>Michał K.</h4>
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<ol>
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</ol>
 
<h3></h3>
<h3></h3>

Revision as of 10:52, 27 October 2008

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Preparation of linker_alpha (BBa_K103009)

Piotr

  1. Isolation of plasmid from culture inoculated on previous day (pSB2K3 + linker_alpha (BBa_K103009)).
  2. Control digest of isolated plasmids with EcoRI and PstI (Orange buffer). Gel electrophoresis - still no proper clones found.

Preparation of linker_omega (BBa_K103013)

Piotr

  1. Isolation of plasmid from culture inoculated on previous day (pSB2K3 + linker_omega (BBa_K103013)).
  2. Control digest of isolated plasmids with EcoRI and PstI (Orange buffer). Gel electrophoresis - proper clones found.

Preparation of OmpA-linker-omega-linker (BBa_K103016)

Piotr

  1. Isolation of plasmid from culture inoculated on previous day (pACYC177 + OmpA-linker-omega-linker (BBa_K103016)).
  2. Control digest of isolated plasmids with EcoRI and PstI (Orange buffer). Gel electrophoresis - no proper clones found.

Preparation of vector for pT7 constructs

Michał K.

Inoculation of colonies from plate with ligation of pET15b+OmpA_omega without XbaI to liquid LB + ampicillin.

Preparation of pLac_OmpA_omega

Piotr

Inoculation of colonies from plate with ligation of pSB2K3 + pLac_OmpA_omega (without EcoRI site) to liquid LB + kanamycin.

Preparation of AID

Michał K.

  1. Colony PCR with AIDlNrH and AIDpLinB primers on colonies from plates with transformations pSB1A3+ AID (annealing temperature - 55°C, 60 s of elongation step).
  2. Inoculation of confirmed colonies to liquid LB + ampicillin.

Preparation of BioBricks

Michał K.

    Piotr

    1. Transformation of TOP10 with ligation pMPMT5+AID without EcoRI site.
    2. Tranformants planting on LB with tetracycline.