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      <title>CSI LAB: Dna finger-printing--Marchetti Elena by ElenaM98</title>
      <link>https://padlet.com/ele9_marchetti/geb06709a4mt</link>
      <description>Realizzato con difficoltà</description>
      <language>en-us</language>
      <pubDate>2016-11-29 14:58:16 UTC</pubDate>
      <lastBuildDate>2026-03-17 01:28:26 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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         <title>Elena Marchetti</title>
         <author>ele9_marchetti</author>
         <link>https://padlet.com/ele9_marchetti/geb06709a4mt/wish/140527129</link>
         <description><![CDATA[<div><strong>Was it possible to identify people in the past? How?<br></strong>Yes it was. in the past criminals were identifed by his face, blood group,teeth impression and after 1901 also by finger-prints.<br>No, it was only possible to exclude suspects. Finger printing&nbsp; could identity people since 1901.</div><div><strong>When was used first DNA finger printing?<br></strong>Dna finger-printing was&nbsp; developed in 1984 by an english geneticist called<del> alec J jeffey.</del><strong> Alec J. Jeffreys. </strong>DNA fingerprinting is used for first time as an identification technique OF A GHANA' CHILD in 1985. FIRST TEST For a criminal conviction, Based on DNA evidence in USA IS Introduced in 1988.<br><br></div><div><strong>Where can DNA be obtained from?<br></strong>DNA can be found in white blood cell, urine, <del>fecis</del>, <strong>feces</strong>, semen, vaginal fluids ,skin dandruff,hair follicle cells, nasal <del>mucuose</del> <strong>mucouse</strong> and sweat stain.( blah)<strong><br></strong><br></div><div><strong>Who invented RFLP technique? When?<br></strong>In the 70s, the discovery of restriction enzymes,<br>Bacterial transformation and gel electrophoresis<br>agarose has initiated the development of&nbsp; genetic engineering.<br>1978 Nobel laureate W. Arber, Nathan D. &amp;<br>H. O'Smith, for the discovery of enzymes<br>restriction, <del>created</del> <strong>found out</strong>&nbsp; the <strong>restriction fragment length polymorphism</strong> or <strong>RFLP.</strong></div><div><strong>What is a restriction enzyme?<br></strong>. In RFLP analysis , DNA is broken into pieces by restriction enzime,&nbsp; at certain point, specific <del>fot&nbsp; </del><strong>for</strong> any enzime.<br>because of every man has a little different to each other the lenght of pieces is different.<strong><br><br>What is restriction enzyme role in nature?<br></strong>Restriction enzymes have been developed inside bacteria to prevent viral infection.they cuton pieces duoble stand viral DNA<strong>.</strong></div>]]></description>
         <enclosure url="" />
         <pubDate>2016-11-29 15:20:00 UTC</pubDate>
         <guid>https://padlet.com/ele9_marchetti/geb06709a4mt/wish/140527129</guid>
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      <item>
         <title></title>
         <author>ele9_marchetti</author>
         <link>https://padlet.com/ele9_marchetti/geb06709a4mt/wish/141609528</link>
         <description><![CDATA[<div><strong>What is the basic principle of gel electrophoresis?<br></strong>the basic principle of gel electrophoresis is his structure like a net which can separate the pieces of dna whith different lenght.<strong><br></strong><br></div><div><strong>Why does DNA migrate toward positive electrode?<br></strong>because&nbsp; it has a negative <del>charhe</del> for <del>gro</del> many phospate<strong><br></strong><br></div><div><strong>What is the TBE composition?</strong></div><div>It's a solution of Tris-borate-EDTA (ethylenediaminetetraacetic acid). The TBE buffer is particularly useful in the separation of small DNA fragments, like the resulting from the digestion of restriction enzymes.(preparation of agarose electrophoretic gels)TBE has A good buffering capacity (pH 8,8) and provides an accurate resolution.</div><div><strong>Why is important to add Mg ions? Are they co-enzymes or cofactors?<br>mg 2+ are very important because they starded the reaction,; they are inorgarnic molecules so are cofactors.<br></strong><br></div><div><strong>How can DNA be detected in agarose gel?<br><br>DNA be detected in agarose gel </strong>with two specific dyes, one long and slow, the other short and fast</div><div><strong><br></strong><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2016-12-04 17:45:00 UTC</pubDate>
         <guid>https://padlet.com/ele9_marchetti/geb06709a4mt/wish/141609528</guid>
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         <title></title>
         <author>ele9_marchetti</author>
         <link>https://padlet.com/ele9_marchetti/geb06709a4mt/wish/141609576</link>
         <description><![CDATA[<div><strong>Why are DNA dying dangerous for human health?Dying dna can be cacerogenic causo of dyer  and create muation if it </strong>makes contact whit normal cells, assorbed by the skin and immediatly  breated.</div><div><strong>What should be done to prepare an agarose gel?  </strong><a href="https://www.youtube.com/watch?v=wXiiTW3pflM"><strong>https://www.youtube.com/watch?v=wXiiTW3pflM</strong></a><strong><br>you should unit togheter agarose ( variable 0.6 to 3%) and TBE. </strong>set the cap on the jar with the solution and move on to the microwave.Be careful at high temperatures and wait time for the dissolution of t agarose. Use always different gloves. Finally put the gel in eletrophoresis support  whit the mask for wells. eliminate bubbles. wait 20 minutes and gel is finished</div><div><strong>What should not be done preparing an agarose gel? close the tap., use the same gloves or move the gel while is solidifing.</strong></div>]]></description>
         <enclosure url="" />
         <pubDate>2016-12-04 17:45:44 UTC</pubDate>
         <guid>https://padlet.com/ele9_marchetti/geb06709a4mt/wish/141609576</guid>
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      <item>
         <title>What role does DNA evidence play in solving crimes?</title>
         <author>ele9_marchetti</author>
         <link>https://padlet.com/ele9_marchetti/geb06709a4mt/wish/142098425</link>
         <description><![CDATA[<div><strong>14"  Why has DNA received a  lot of media attention?<br>Because it has a good power of discrimination and it's better than a  eyewitness testimony.</strong></div><div><strong>36"   How long has DNA  been used to identify people?<br>from '85, using different tecniques.<br>52"   The techniques used nowadays are more sensitive. How much DNA is needed to do a test? from 50 ng to 1 ng.<br>1'26 "How many cells are needed to get a full profile?<br>full profile can be found in 3 or 4 cells<br>1' 46" In what conditions must the exhibit be kept?<br>to keep in good conditons you can freeze ordry it.</strong></div><div><strong>1' 52" How long does DNA last if taken in good conditions?<br>DNA will last essentially forever.</strong></div>]]></description>
         <enclosure url="" />
         <pubDate>2016-12-06 17:50:58 UTC</pubDate>
         <guid>https://padlet.com/ele9_marchetti/geb06709a4mt/wish/142098425</guid>
      </item>
      <item>
         <title>Valeria Fregni</title>
         <author>vfregniddt</author>
         <link>https://padlet.com/ele9_marchetti/geb06709a4mt/wish/148859854</link>
         <description><![CDATA[<div>I contenuti essenziali sono presenti. Si colgono degli approfondimenti pur nella inesistente cura per le maiuscole, il carattere e lo spelling. Puoi impegnarti di più: la videoscrittura è molto usata nel mondo moderno...! Mancano delle parti del portfolio</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-01-23 20:11:15 UTC</pubDate>
         <guid>https://padlet.com/ele9_marchetti/geb06709a4mt/wish/148859854</guid>
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