Team:Warsaw/Calendar-Main/4 August 2008
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- | <h3> Cloning of truncated fragment of protein A</h3> | + | <h3> Cloning of truncated fragment of protein A (ΔA)</h3> |
<h4>Piotr</h4> | <h4>Piotr</h4> | ||
- | <p>Inoculation of some pACYC177+OmpA_alpha + | + | <p>Inoculation of some <a href=phttps://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-deltaA-alpha>pACYC177+OmpA_alpha + ΔA</a> and <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BOmpA-deltaA-omega>pACYC177+OmpA_omega + ΔA</a> colonies of tranformants.</p> |
- | <h3>Checking | + | <h3>Checking <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-omega-A-alpha>OmpA_omega_ΔA_alpha</a> expression</h3><h4>Piotr</h4> |
- | <p>Inoculation of | + | <p>Inoculation of <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-omega-A-alpha>OmpA_omega_ΔA_alpha</a> with inductor (0,5 mmol/mL IPTG) and negative control without IPTG.</p> |
- | <h3>Checking if | + | <h3>Checking if <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-omega-A-alpha>OmpA_omega_ΔA_alpha</a> gives ampicillin resistance</h3><h4>Emilia</h4> |
- | <p>Inoculation of | + | <p>Inoculation of <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-omega-A-alpha>OmpA_omega_ΔA_alpha</a> into various IPTG concentrations: 0, 0.1, 0.25, 0.5, 0.75, 1 mmol/mL.</p> |
- | <h3>Preparing pACYC177+ | + | <h3>Preparing pACYC177+OmpA_omega_ΔA construct</h3><h4>Michał K.</h4> |
- | <ol><li><a href="https://2008.igem.org/Wiki/Team:Warsaw/protocols#digest">Digest</a> of pACYC177+ | + | <ol><li><a href="https://2008.igem.org/Wiki/Team:Warsaw/protocols#digest">Digest</a> of <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-omega-A-alpha>pACYC177+OmpA_omega_ΔA_alpha</a> (from 25 July) with BamHI and NotI (BamHI buffer). DNA ends <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#blunting">blunting</a> with Klenow fragment (3 hr). </li> |
- | + | <li>Gel elctrophoresis (<a href="https://2008.igem.org/Team:Warsaw/Calendar-Main/4_August_2008#fig1">Fig. 1</a>) and <a href="https://2008.igem.org/Wiki/Team:Warsaw/protocols#DNA_isolation_from_agarose_gel">gel-out</a> of proper band - 4300 bp. </li> | |
- | <li><a href="https://2008.igem.org | + | <li>Overnight <a href="https://2008.igem.org/Wiki/Team:Warsaw/protocols#ligation">ligation</a> of isolated DNA fragment. </li> |
- | + | </ol> | |
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+ | <a name="fig1"><img src="https://static.igem.org/mediawiki/2008/1/17/Gucio.jpg" width=240/></a> <var><b>Fig. 1. </b>Gel-out of pACYC177_OmpA_omega_deltaA_alpha digested with NotI/BamHI after blunting ends.<br> | ||
+ | 1. Marker<br> | ||
+ | 2. pACYC177_OmpA_omega_deltaA_alpha <br></var> | ||
Latest revision as of 10:50, 29 October 2008
Cloning of truncated fragment of protein A (ΔA)PiotrInoculation of some pACYC177+OmpA_alpha + ΔA and pACYC177+OmpA_omega + ΔA colonies of tranformants. Checking OmpA_omega_ΔA_alpha expressionPiotrInoculation of OmpA_omega_ΔA_alpha with inductor (0,5 mmol/mL IPTG) and negative control without IPTG. Checking if OmpA_omega_ΔA_alpha gives ampicillin resistanceEmiliaInoculation of OmpA_omega_ΔA_alpha into various IPTG concentrations: 0, 0.1, 0.25, 0.5, 0.75, 1 mmol/mL. Preparing pACYC177+OmpA_omega_ΔA constructMichał K.
1. Marker 2. pACYC177_OmpA_omega_deltaA_alpha
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