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      <title>DNA Finger-Printing by alicerovigatti</title>
      <link>https://padlet.com/alice_rovigatti1/tpatu96pm3xn</link>
      <description>Modulo CLIL</description>
      <language>en-us</language>
      <pubDate>2017-11-28 16:21:54 UTC</pubDate>
      <lastBuildDate>2025-02-24 23:00:59 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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         <title></title>
         <author>alice_rovigatti1</author>
         <link>https://padlet.com/alice_rovigatti1/tpatu96pm3xn/wish/211017114</link>
         <description><![CDATA[]]></description>
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         <pubDate>2017-11-28 16:53:13 UTC</pubDate>
         <guid>https://padlet.com/alice_rovigatti1/tpatu96pm3xn/wish/211017114</guid>
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      <item>
         <title>Are we all different? (1)</title>
         <author>alice_rovigatti1</author>
         <link>https://padlet.com/alice_rovigatti1/tpatu96pm3xn/wish/217858172</link>
         <description><![CDATA[<div><strong><mark>Was it possible to identify people in the past? How?<br></mark></strong>Yes, in the past it was possible to identify people  by the eyes color, finger-print, jewels, bite impression. Human identification has been historically based on finger-printing since 1901.<br><strong><mark>When was used first DNA finger printing?</mark></strong><br>DNA finger printing was used for the first time in 1988 to solve a case of rape and murder.<br><strong><mark>Where can DNA be obtained from?</mark></strong><mark><br></mark>DNA can be obtained from blood (only white cells), semen, hair with roots, skin, dandruff, sweat stains, urine, feces, vaginal fluids, liquid in contact of mucosa, nasal secretion.<br><strong><mark>Who invented RFLP technique? When?<br></mark></strong>RFLP technique was inveted by Alcec J. Jeffrey, molecular geneticist at the University of Leicester UK, in 1984.</div><div><strong><mark>What is a restriction enzyme?</mark></strong><strong><br></strong>Restriction enzyme is a protein that cuts DNA at particular base sequences.</div><div><strong><mark>What is restriction enzyme role in nature?</mark></strong><strong><br></strong>The role of the restriction enzyme inside bacteria is to protect  them against viral DNA infection.</div>]]></description>
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         <pubDate>2017-12-22 14:22:07 UTC</pubDate>
         <guid>https://padlet.com/alice_rovigatti1/tpatu96pm3xn/wish/217858172</guid>
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         <title>DNA from the crime scene and suspects (2)</title>
         <author>alice_rovigatti1</author>
         <link>https://padlet.com/alice_rovigatti1/tpatu96pm3xn/wish/217861792</link>
         <description><![CDATA[<div><strong><mark>What is the basic principle of gel electrophoresis?</mark></strong><strong><br></strong>The basic principle of gel electrophoresis, that is agarose gel, it's that it is a molecular sieve. </div><div><strong><mark>Why does DNA migrate toward positive electrode?<br></mark></strong>DNA migrates toward positive electrode at pH 8.0 it's negatively charged.<br><strong><mark>What is the TBE composition?</mark></strong><strong><br></strong>The TBE composition is: NaCl, Tris-HCl and Mg<sup>2+</sup> ions.</div><div><strong><mark>Why is important to add Mg ions? Are they co-enzymes or cofactors?</mark></strong><strong><br></strong>It's important to add Mg ions because they favor the digestion of DNA. They are cofactors.</div><div><strong><mark>How can DNA be detected in agarose gel?<br></mark></strong>DNA can be detected in agarose gel by using an intercalant dye and putting it under UV linght (transilluminator).<strong><br></strong><strong><mark>Why are DNA dyes dangerous for human health?</mark></strong><strong><br></strong>DNA dyes are dangerous for human health because they contain mutagenics substances, dangerous for our DNA.</div><div><strong><mark>What should be done to prepare an agarose gel?</mark></strong><strong><br></strong>To prepare an agaorose gel we should: put agarose powder in a conic flask; add 10mL of TAE; put the conic flask in a microwave owen until the solution is completely transparent; pour the solution in the gel tray and create wells by using a comb.</div><div><strong><mark>What should not be done preparing an agarose gel?<br></mark></strong>When we are preparing an agarose gel we shouldn't done: pour quickly the solution in the gel tray; don't leave bubbles in the gel; don't leave the conic flask inside the microwave without checking it. <br><strong><mark>Which piece of information can be find out from a DNA pattern bands?</mark></strong><strong><br></strong>From DNA pattern bands we can discover who is the culprit of a crime.</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-12-22 14:51:00 UTC</pubDate>
         <guid>https://padlet.com/alice_rovigatti1/tpatu96pm3xn/wish/217861792</guid>
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      <item>
         <title>Pyramid discussion</title>
         <author>alice_rovigatti1</author>
         <link>https://padlet.com/alice_rovigatti1/tpatu96pm3xn/wish/217868059</link>
         <description><![CDATA[<div><strong><mark>At the beginning, read the list and&nbsp; individually select the three items you think influence more electrophoresis result.</mark></strong><br>My group (Bergamini, Scainelli and me) selected these four items : presence of Mg ions; buffer solution pH; agarose gel concentration and presence of bubbles in the gel.<br><strong><mark>&nbsp;Later on you will discuss your choises in pairs you should find an agreement on three items, some of them must be "trade off" and you must find compromises.<br></mark></strong>We compared our decisions with another group (Bretta and Brina) and we discussed about our choices. They chose: voltage applied to the electrophoretic cell; presence of Mg ions; buffer solution pH. Finally togheter we decided what items were important.<strong><br></strong><strong><mark>In group of four you should discuss once more the best three items of each group.</mark></strong><strong><br></strong>At the end of the discussion we decided: presence of Mg ions; buffer solution pH; agarose gel concentration.<br><strong><mark>Class discussion on results.<br></mark></strong><strong>The three most important items are: </strong>voltage applied to the electrophoretic cell because we need the right voltage to avoid destroying the gel; buffer solution pH because the DNA has to be negatively charged; agarose gel concentration because agarose gel is a molecular sieve that depends on the concentration of agarose (for small fragments we need an high concentration); presence of bubbles in the gel because if there are bubbles DNA won't run correctely.</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-12-22 15:34:50 UTC</pubDate>
         <guid>https://padlet.com/alice_rovigatti1/tpatu96pm3xn/wish/217868059</guid>
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      <item>
         <title>Lab report</title>
         <author>alice_rovigatti1</author>
         <link>https://padlet.com/alice_rovigatti1/tpatu96pm3xn/wish/218214875</link>
         <description><![CDATA[<div>Ho caricato il pdf perchè il PowerPoint è troppo pesante.</div>]]></description>
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         <pubDate>2017-12-31 11:13:01 UTC</pubDate>
         <guid>https://padlet.com/alice_rovigatti1/tpatu96pm3xn/wish/218214875</guid>
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         <title>What role does DNA evidence play in solving crimes?</title>
         <author>alice_rovigatti1</author>
         <link>https://padlet.com/alice_rovigatti1/tpatu96pm3xn/wish/218222255</link>
         <description><![CDATA[<div><strong><mark>Why has DNA received a  lot of media attention?</mark></strong><strong><br>DNA has received a lot of media attention because it has a fantastic power of discrimination. </strong></div><div><strong><mark>How long has DNA  been used to identify people?</mark></strong><strong><br>DNA has been used to identify people since the mid 80s, but now technologies are more developed.<br></strong><strong><mark>The techniques used nowadays are more sensitive. How much DNA is needed to do a test?</mark></strong><strong><br>To do a test it's needed less than a gram of DNA.</strong></div><div><strong><mark>How many cells are needed to get a full profile?</mark></strong><strong><br>To get a full profile three or four cells are needed.</strong></div><div><strong><mark>In what conditions must the exhibit be kept?</mark></strong><strong><br>The exhibit must be kept dry or frozen.</strong></div><div><strong><mark>How long does DNA last if taken in good conditions?<br></mark></strong><strong>DNA taken in good conditions will last essentially forever.</strong></div>]]></description>
         <enclosure url="" />
         <pubDate>2017-12-31 15:03:09 UTC</pubDate>
         <guid>https://padlet.com/alice_rovigatti1/tpatu96pm3xn/wish/218222255</guid>
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      <item>
         <title>Transcript of ppt</title>
         <author>alice_rovigatti1</author>
         <link>https://padlet.com/alice_rovigatti1/tpatu96pm3xn/wish/219443290</link>
         <description><![CDATA[]]></description>
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         <pubDate>2018-01-08 17:03:33 UTC</pubDate>
         <guid>https://padlet.com/alice_rovigatti1/tpatu96pm3xn/wish/219443290</guid>
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      <item>
         <title>Thinglink</title>
         <author>alice_rovigatti1</author>
         <link>https://padlet.com/alice_rovigatti1/tpatu96pm3xn/wish/219565044</link>
         <description><![CDATA[]]></description>
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         <pubDate>2018-01-08 21:49:06 UTC</pubDate>
         <guid>https://padlet.com/alice_rovigatti1/tpatu96pm3xn/wish/219565044</guid>
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      <item>
         <title>Thinglink</title>
         <author>alice_rovigatti1</author>
         <link>https://padlet.com/alice_rovigatti1/tpatu96pm3xn/wish/219566083</link>
         <description><![CDATA[]]></description>
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         <pubDate>2018-01-08 21:53:35 UTC</pubDate>
         <guid>https://padlet.com/alice_rovigatti1/tpatu96pm3xn/wish/219566083</guid>
      </item>
      <item>
         <title>Thinglink</title>
         <author>alice_rovigatti1</author>
         <link>https://padlet.com/alice_rovigatti1/tpatu96pm3xn/wish/219566862</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://www.thinglink.com/scene/1007044483277127683" />
         <pubDate>2018-01-08 21:57:20 UTC</pubDate>
         <guid>https://padlet.com/alice_rovigatti1/tpatu96pm3xn/wish/219566862</guid>
      </item>
      <item>
         <title>Glossary</title>
         <author>alice_rovigatti1</author>
         <link>https://padlet.com/alice_rovigatti1/tpatu96pm3xn/wish/219569348</link>
         <description><![CDATA[<div><mark>Iris</mark>: iride<br><mark>Double strand</mark>: doppio filamento<br><mark>Dandruff</mark>: forfora<br><mark>Sample</mark>: campione<br><mark>RFLP</mark>: restriction fragment length polymorphism<br><mark>Frictional</mark> <mark>force</mark>: forza d'attrito<br><mark>To repel</mark>: respingere<br><mark>Rate of </mark>migration: velocità<br><mark>Stain</mark>: colorante<br><mark>Bite impression</mark>: il morso <br><mark>Auricle shape</mark>: forma delle orecchie<br><mark>Palindromic sequence</mark>: sequenza palindromica<br><mark>Finger-print</mark>: impronta digitale</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-01-08 22:09:31 UTC</pubDate>
         <guid>https://padlet.com/alice_rovigatti1/tpatu96pm3xn/wish/219569348</guid>
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