Team:Warsaw/Calendar-Main/16 October 2008

From 2008.igem.org

Revision as of 20:28, 27 October 2008 by Smaegol (Talk | contribs)

Gallery Bricks Notebook Team Project Home


Previous day
return to main notebook page
Previous entry
next notebook entry

 


Preparation of linker_alpha (BBa_K103009)

Michał K.

  1. Isolation of plasmids from culture inoculated on previous day.
  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)

Michał K.

Inoculation of colonies from plate with new ligation of pACYC177 + OmpA-linker-omega-linker (BBa_K103016) to LB with kanamycin.

Preparation of alpha_linker under PT7 (BBa_K103019)

Michał K.

  1. Control digest of isolated plasmid - pSB1A3 carrying alpha_linker under PT7 (BBa_K103019) fragment (14 October) with EcoRI and PstI (Orange buffer). Gel electrophoresis - proper clones found.
  2. Overnight digest pSB1A3 carrying alpha_linker under PT7 (BBa_K103019) with EcoRI and BcuI (BamHI buffer).

Preparation of AID under pBAD/araC (BBa_K103002)

Michał K.

  1. Isolation of plasmids from culture inoculated on previous day (pSB1A3 + AraC+pBAD+AID).
  2. Control digest of isolated plasmids with EcoRI and PstI (Orange buffer). Gel electrophoresis - still no proper clones found.
  3. Repetition of overnight ligation of isolated DNA fragments: pSB1A3 + AraC+pBAD+AID.

Preparation of pLac_OmpA_alpha

Michał K.

  1. Isolation of plasmids from culture inoculated on previous day - pSB2K3_pLac_OmpA_ + alpha2.
  2. Control digest of isolated plasmids with EcoRI and PstI (Orange buffer). Gel electrophoresis - we found good clones.