Team:Warsaw/Calendar-Main/13 October 2008

From 2008.igem.org

(Difference between revisions)
Line 49: Line 49:
<ol>
<ol>
<li><a href=https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#digest>Digest</a> of  
<li><a href=https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#digest>Digest</a> of  
-
<a href=http://partsregistry.org/Part:pSB2K3>pSB2K3</a> + pLac_OmpA_omega with BcuI and SacI (SacI buffer), <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#removing">dephosphorylation</a> with CIAP. </li>
+
<a href=http://partsregistry.org/Part:pSB2K3>pSB2K3</a> + <a href=http://partsregistry.org/Part:BBa_K103018>OmpA_linker_omega_linker under Plac</a> with BcuI and SacI (SacI buffer), <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#removing">dephosphorylation</a> with CIAP. </li>
-
<li> <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcr">PCR</a> on alpha PCR product from 10 September using  
+
<li> <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcr">PCR</a> on alpha PCR product from <a href=https://2008.igem.org/Team:Warsaw/Calendar-Main/10_October_2008>10 October</a> using  
<a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#AlphaL+SacI">AlphaL+SacI</a> and <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#LinP_BS2">LinP_BS2</a>
<a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#AlphaL+SacI">AlphaL+SacI</a> and <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#LinP_BS2">LinP_BS2</a>
-
primers (annealing temperature 58 &deg;C; elongation length 60s) to obtain alpha2 fragment with proper restriction sites. </li>
+
primers (annealing temperature 58 &deg;C; elongation length 60s) to obtain alpha2 fragment with proper restriction sites (SacI and BcuI). </li>
-
<li>Gel electrophoresis and <a href="https://2008.igem.org/Wiki/Team:Warsaw/protocols#DNA_isolation_from_agarose_gel">gel-out</a> of proper band 600 bp for alpha2 PCR product and 3000 bp for <a href=http://partsregistry.org/Part:pSB2K3>pSB2K3</a> + pLac_OmpA_. </li>
+
<li>Gel electrophoresis and <a href="https://2008.igem.org/Wiki/Team:Warsaw/protocols#DNA_isolation_from_agarose_gel">gel-out</a> of proper bands (600 bp for alpha2 PCR product and 3000 bp for <a href=http://partsregistry.org/Part:pSB2K3>pSB2K3</a> + OmpA_linker under PLac promoter fragment). </li>
<li><a href=https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#digest>Digest</a> of  
<li><a href=https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#digest>Digest</a> of  
isolated PCR product (alpha2 fragment) with SacI and BcuI (SacI buffer). </li>
isolated PCR product (alpha2 fragment) with SacI and BcuI (SacI buffer). </li>
Line 63: Line 63:
-
<li> Overnight <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#ligation">ligation</a> of DNA fragments: <a href=http://partsregistry.org/Part:pSB2K3>pSB2K3</a>_pLac_OmpA_ + alpha2.</li>
+
<li> Overnight <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#ligation">ligation</a> of DNA fragments: <a href=http://partsregistry.org/Part:pSB2K3>pSB2K3</a> with lactose promoter and OmpA_linker  + alpha2.</li>
</ol>
</ol>

Revision as of 23:41, 27 October 2008

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. PCR on pACYC177+OmpA_omega_deltaA_alpha plasmid using LinLSXNE and AlphaPSpe primers (annealing temperature 58 °C; elongation length 60s) to obtain linker_alpha (BBa_K103009) fragment.
  2. Gel electrophoresis and gel-out of proper band 600 bp - linker_alpha (BBa_K103009) PCR product.
  3. Digest of isolated PCR product linker_alpha (BBa_K103009) with EcoRI and BcuI (BamHI buffer).
  4. Clean-up of digested PCR product.
  5. Overnight ligation of DNA fragments: pSB2K3 + linker_alpha (BBa_K103009).

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

Michał K.

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

Preparation of alpha_linker under PT7 (BBa_K103019)

Michał K.

Inoculation of colonies from plate with ligation of pSB1A3 carrying alpha_linker under PT7 (BBa_K103019) fragment to liquid LB + ampicillin.

Preparation of omega_linker under PT7 (BBa_K103020)

Michał K.

Inoculation of colonies from plate with ligation of pSB2K3 + omega_linker under PT7 (BBa_K103020) to liquid LB + kanamycin.

Preparation of AID under pBAD/araC (BBa_K103002)

Michał K.

Overnight ligation of DNA fragments: pSB1A3 (from 6 October) + AID under pBAD/araC (BBa_K103002) (from 10 October).

Preparation of OmpA_linker_alpha_linker under Plac (BBa_K103017)

Michał K.

  1. Digest of pSB2K3 + OmpA_linker_omega_linker under Plac with BcuI and SacI (SacI buffer), dephosphorylation with CIAP.
  2. PCR on alpha PCR product from 10 October using AlphaL+SacI and LinP_BS2 primers (annealing temperature 58 °C; elongation length 60s) to obtain alpha2 fragment with proper restriction sites (SacI and BcuI).
  3. Gel electrophoresis and gel-out of proper bands (600 bp for alpha2 PCR product and 3000 bp for pSB2K3 + OmpA_linker under PLac promoter fragment).
  4. Digest of isolated PCR product (alpha2 fragment) with SacI and BcuI (SacI buffer).
  5. Clean-up of digested PCR product.
  6. Overnight ligation of DNA fragments: pSB2K3 with lactose promoter and OmpA_linker + alpha2.
Fig. 1.Go2_13_10_2008