Team:Warsaw/Calendar-Main/16 June 2008
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- | + | <h3>Preparation of constructs: OmpA_alpha and OmpA_omega</h3> | |
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- | <h3>Preparation of constructs | + | |
<h4>Michał K.</h4> | <h4>Michał K.</h4> | ||
<p> | <p> | ||
<ol> | <ol> | ||
- | <li> <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcr">PCR</a> on pB30D plasmid with | + | <li> <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcr">PCR</a> on <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pB30D>pB30D</a> plasmid with |
<a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#OmpaL_N">OmpaL_N</a> and <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#OmpaP_link">OmpaP_link</a> | <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#OmpaL_N">OmpaL_N</a> and <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#OmpaP_link">OmpaP_link</a> | ||
primers (15 cycles, elongation duration 45 s, annealing temperature 63°C). </li> | primers (15 cycles, elongation duration 45 s, annealing temperature 63°C). </li> | ||
- | <li> <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcr">PCR</a> on pUC19 plasmid with | + | <li> <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcr">PCR</a> on <a href=http://www.fermentas.com/techinfo/nucleicacids/mappuc1819.htm>pUC19</a> plasmid with |
<a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#AlphaL_link">AlphaL_link</a> and <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#AlphaP_XB">AlphaP_XB</a> | <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#AlphaL_link">AlphaL_link</a> and <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#AlphaP_XB">AlphaP_XB</a> | ||
primers (20 cycles, elongation duration 45 s, annealing temperature 63°C).</li> | primers (20 cycles, elongation duration 45 s, annealing temperature 63°C).</li> | ||
- | <li> <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcr">PCR</a> on pUC19 plasmid with | + | <li> <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcr">PCR</a> on <a href=http://www.fermentas.com/techinfo/nucleicacids/mappuc1819.htm>pUC19</a> plasmid with |
<a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#OmegaL_link">OmegaL_link</a> and <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#OmegaP_EPB">OmegaP_EPB</a> | <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#OmegaL_link">OmegaL_link</a> and <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#OmegaP_EPB">OmegaP_EPB</a> | ||
primers (20 cycles, elongation duration 30 s, annealing temperature 58°C).<br> | primers (20 cycles, elongation duration 30 s, annealing temperature 58°C).<br> | ||
As a result we got three PCR products: OmpA_linker and two fragments of TEM1 beta-lactamese: linker_alpha and linker_omega. </li> | As a result we got three PCR products: OmpA_linker and two fragments of TEM1 beta-lactamese: linker_alpha and linker_omega. </li> | ||
- | <li> Gel electrophoresis of PCR products and <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#DNA_isolation_from_agarose_gel">gel-out</a> of proper bands (OmpA_linker - 500 bp, linker_alpha - 600 bp and linker_omega - 350 bp).</li> | + | <li> Gel electrophoresis of PCR products (<a href="https://2008.igem.org/wiki/index.php?title=Team:Warsaw/Calendar-Main/16_June_2008#fig1">Fig. 1</a>) and <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#DNA_isolation_from_agarose_gel">gel-out</a> of proper bands (OmpA_linker - 500 bp, linker_alpha - 600 bp and linker_omega - 350 bp).</li> |
+ | <li>Electrophoresis to estimate the concentration of isolated DNA.</li> | ||
</ol></p> | </ol></p> | ||
+ | <a name="fig1"><img src="https://static.igem.org/mediawiki/2008/a/a3/PCR_Ompa_Alpha_Omega_WAW.jpg" width=300/></a> | ||
+ | <var><b>Fig. 1.</b> PCR products: linker_alpha (lane 2), linker_omega (lane 3), OmpA_linker (lane 4)</var> | ||
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+ | <h3> Blue/white and rifampicin test #1</h3> | ||
+ | <h4>Michał L., Ewa</h4> | ||
+ | <ol> | ||
+ | <li>Colony <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcr">PCR</a>.<br> | ||
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+ | Template: DNA isolated from white colonies<br> | ||
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+ | Primers: <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#pZCseqL">pZCseqL</a> and <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#pZCseqR">pZCseqR</a><br> | ||
+ | <br> | ||
+ | <table id="result"> | ||
+ | <tr><th colspan="3">Colony PCR program</th></tr> | ||
+ | <tr><th>Temperature</th><th>Time</th><th>No. of cycles</th></tr> | ||
+ | <tr><td>94°C</td><td>4:00</td></tr> | ||
+ | <tr><td>94°C</td><td>0:30</td><td rowspan="3">28 cycles</td></tr> | ||
+ | <tr><td>48°C</td><td>0:45</td></tr> | ||
+ | <tr><td>72°C</td><td>1:30</td></tr> | ||
+ | <tr><td>72°C</td><td>10:00</td></tr> | ||
+ | <tr><td>4°C</td><td>infinite</td></tr> | ||
+ | </table> | ||
+ | <br> | ||
+ | <li>DNA gel electrophoresis of PCR products. <a href="https://2008.igem.org/wiki/index.php?title=Team:Warsaw/Calendar-Main/16_June_2008#fig2">Fig. 2.</a></li> | ||
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+ | <li>Gel-out of proper products (~1200 bp).</li> | ||
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+ | <li>Sequencing of proper fragments using primer <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#pZCseqL">pZCseqL</a>.</li></ol> | ||
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+ | <a name="fig2"><img src="https://static.igem.org/mediawiki/2008/0/0c/Colony_PCR_pZC_WAW.jpg" width=400/></a> | ||
+ | <var><b>Fig. 2.</b> 1 - DNA ladder; 2 to 11 - colony PCR products (lacZ' gene) from blue and white colonies.</var> | ||
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Latest revision as of 14:50, 26 October 2008
Preparation of constructs: OmpA_alpha and OmpA_omegaMichał K.
Blue/white and rifampicin test #1Michał L., Ewa
Fig. 2. 1 - DNA ladder; 2 to 11 - colony PCR products (lacZ' gene) from blue and white colonies.
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