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      <title>GROUP ACTIVITY: RECOMBINANT TECHNOLOGY by SARAH KALTHOM BINTI RIZA AMARALLAH BEG Moe</title>
      <link>https://padlet.com/m3811276/h7x5vfdwyqvsu3z2</link>
      <description>Group 2 
Lisa
Pei Yong
Sarah 
Danial</description>
      <language>en-us</language>
      <pubDate>2021-11-05 08:16:15 UTC</pubDate>
      <lastBuildDate>2021-11-07 15:54:49 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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      <item>
         <title>Question 4</title>
         <author>m3811276</author>
         <link>https://padlet.com/m3811276/h7x5vfdwyqvsu3z2/wish/1869465899</link>
         <description><![CDATA[<div>a) Transformed bacterial cell will stay alive.&nbsp;Transformed bacteria cell with recombinant plasmid able to grow and amplify itself while the transformed bacteria cell with no plasmid dies.<br><br>b) It will die.</div>]]></description>
         <enclosure url="" />
         <pubDate>2021-11-05 08:19:10 UTC</pubDate>
         <guid>https://padlet.com/m3811276/h7x5vfdwyqvsu3z2/wish/1869465899</guid>
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      <item>
         <title>Question 3</title>
         <author>m3811276</author>
         <link>https://padlet.com/m3811276/h7x5vfdwyqvsu3z2/wish/1869466036</link>
         <description><![CDATA[<div>a) Mode of action of <em>Eco</em>Rl is sticky ends while the mode of action of <em>Sma</em>l is blunt ends. <em>Eco</em>Rl cuts both DNA strands between base G and base A while <em>Sma</em>l cuts both DNA strands between base C and base G.<br><br>b) i. Sticky ends are staggered<strong> </strong>cut single-stranded ends that cleaved by restriction enzyme <em>Eco</em>Rl.<br>&nbsp; &nbsp; &nbsp;ii. 5'GAATTC3'<br>&nbsp; &nbsp; &nbsp; &nbsp; 3'CTTAAG5'<br>&nbsp; &nbsp; &nbsp;iii. 3<br><br></div>]]></description>
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         <pubDate>2021-11-05 08:19:17 UTC</pubDate>
         <guid>https://padlet.com/m3811276/h7x5vfdwyqvsu3z2/wish/1869466036</guid>
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      <item>
         <title>Question 2</title>
         <author>m3811276</author>
         <link>https://padlet.com/m3811276/h7x5vfdwyqvsu3z2/wish/1869466205</link>
         <description><![CDATA[<div>(a) Q<br><br>(b)&nbsp; - Have selectable genetic markers which are ampicillin resistant gene (<em>amp</em><sup>R</sup>) and <em>lac</em>Z<br>&nbsp; &nbsp; &nbsp; &nbsp;- Able to accept foreign DNA in multiple cloning sites<br>&nbsp; &nbsp; &nbsp; &nbsp;- Able to replicate freely in the host cell.</div><div><br>(c) Recombinant plasmid<br><br>(d) Host cell<br><br>(e)&nbsp; - Able to receive recombinant plasmid through the&nbsp; &nbsp; transformation process.<br>&nbsp; &nbsp; &nbsp; &nbsp;- Able to maintain the structure of the recombinant plasmid from one generation to another.<br>&nbsp; &nbsp; &nbsp; &nbsp;- Able to amplify the recombinant DNA.<br><br>(f) No because the target gene and vector must be cleaved with the same restriction enzyme to produce compatible sticky ends on both the foreign DNA fragments and the plasmid.</div>]]></description>
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         <pubDate>2021-11-05 08:19:25 UTC</pubDate>
         <guid>https://padlet.com/m3811276/h7x5vfdwyqvsu3z2/wish/1869466205</guid>
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      <item>
         <title>Question 1</title>
         <author>m3811276</author>
         <link>https://padlet.com/m3811276/h7x5vfdwyqvsu3z2/wish/1869466434</link>
         <description><![CDATA[<div>a)&nbsp; The technology of recombining DNA molecules in vitro by&nbsp; cutting up DNA molecules and splicing fragments together by different organisms.<br><br>b) Source: Bacterial cell<br>&nbsp; &nbsp; &nbsp;Role: DNA Cloning vector<br><br>c) An enzyme which recognizes and cleave DNA molecule at restriction site.<br><br>d) Restriction site: GGATCC<br>&nbsp; &nbsp; &nbsp;Restriction enzyme: <em>Bam</em>HI<br><br>e) i) 2<br>&nbsp; &nbsp; ii) 4<br><br>f) DNA ligase<br><br>g) Bacteria can reproduce fast.</div>]]></description>
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         <pubDate>2021-11-05 08:19:36 UTC</pubDate>
         <guid>https://padlet.com/m3811276/h7x5vfdwyqvsu3z2/wish/1869466434</guid>
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