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      <title>Third period biotech review by Tina Davies</title>
      <link>https://padlet.com/tinadavies03/w0gziocwm913</link>
      <description>Class contributions to review</description>
      <language>en-us</language>
      <pubDate>2017-03-23 13:34:59 UTC</pubDate>
      <lastBuildDate>2023-07-12 06:36:05 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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         <title>click the + circle in the bottom right corner</title>
         <author></author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162156300</link>
         <description><![CDATA[]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 14:58:04 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162156300</guid>
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         <title></title>
         <author></author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162156540</link>
         <description><![CDATA[]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 14:58:39 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162156540</guid>
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         <title>What happens if you cut through the ORI of a plasmid? </title>
         <author></author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162156602</link>
         <description><![CDATA[<div>  </div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 14:58:47 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162156602</guid>
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         <title>Recombinant DNA</title>
         <author>katiah711</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162157992</link>
         <description><![CDATA[<div>In recombinant DNA, how many cuts are made in the donor DNA? And in the plasmid?&nbsp;<br><br>Answer: 2 in the DNA, 1 in the plasmid</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:02:26 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162157992</guid>
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         <title>GMOS</title>
         <author>20cblank</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162158207</link>
         <description><![CDATA[<div>What are some concerns of GMO critics?<br>-threatens vitality of organisms<br>-causes ecological imbalances<br>-can promote the spread of disease among plants and animals<br>-can change organisms growth rate, metabolism, and response to environmental factors<br>-GMO foods can create possibility to transfer of antibiotic resistant genes<br>-GMOs aren't required to be labeled<br>-human health risk<br>-exposure to new allergens</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:02:59 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162158207</guid>
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      <item>
         <title>GMO Pros</title>
         <author>tmtgill</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162159097</link>
         <description><![CDATA[<div>-enhanced mating advantages<br>-improve the speed of food production<br>-surgery<br>-disease resistance</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:05:06 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162159097</guid>
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         <title>Gene Cloning</title>
         <author>20anakahara</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162159241</link>
         <description><![CDATA[<div>What is gene cloning?<br>the production of multiple copies of a specific gene<br><br>What role do plasmids play in gene cloning?<br>Plasmids are easily manipulated to carry many different genes and enable the rapid production of the desired protein due to the rapid replication.<br><br>In what instances would gene cloning be helpful?<br>For the production of a desired protein.<br><br>How are genomic libraries and cloned genes related?<br>Cloned Genes can be stored in the genomic libraries<br><br>What role does recombinant DNA have in gene cloning?<br>Recombinant DNA is a DNA molecule that has been manipulated to carry nucleotide sequences from two different organisms. If recombinant DNA plasmids are inserted into bacteria and the recombinant bacteria multiply, the resulting bacteria are clones in which the foreign gene is copied and these copies can make copies of its protein.<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:05:26 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162159241</guid>
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         <title>What is Gene Therapy?</title>
         <author>20epetersen</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162159515</link>
         <description><![CDATA[<div>The alteration of genes in order&nbsp;to replace or supplement a defective gene</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:06:09 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162159515</guid>
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      <item>
         <title>What happens if you cut through the ORI of a plasmid? </title>
         <author>20bdemarco</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162159663</link>
         <description><![CDATA[<div>The plasmid will no longer work or be able to reproduce so in recombinant DNA it would not help to make new copies of the wanted protein<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:06:31 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162159663</guid>
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         <title>GEL ELECTROPHORESIS</title>
         <author>20nahmad</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162159715</link>
         <description><![CDATA[<div>Why does DNA move towards the positive pole during electrophoresis?<br><br>DNA has phospate groups which gives it a negative charge and negative always attracts positive. </div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:06:40 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162159715</guid>
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      <item>
         <title>GMO Cons</title>
         <author>tmtgill</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162159986</link>
         <description><![CDATA[<div>-can change the organism's metabolism&nbsp;<br>-growth rate<br>-influence the natural environment<br>-potential health risks<br>-cause ecological imbalances<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:07:22 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162159986</guid>
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         <title>Gel Electrophoresis</title>
         <author>18vrana</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162160064</link>
         <description><![CDATA[<div>Why is it important for crime lab technicians to have organized and careful recording techniques?&nbsp;<br><br>Answer: So that the specimen or solutions being tested do not get contaminated and to make sure you are identifying the correct suspect.<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:07:33 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162160064</guid>
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         <title>PCR</title>
         <author>20cblank</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162160138</link>
         <description><![CDATA[<div>What is PCR?<br>-polymerase chain reaction<br>-technique by which a specific segment of a DNA molecule can be targeted and quickly amplified in the laboratory<br>-starting with a minute sample automated PCR can generate billions of copies of a DNA segment in just a few hours producing enough DNA to allow a DNA profile to be constructed<br>STEPS:<br>1. the reaction mixture is heated to separate the strands of the DNA double helixes<br>2. the strands are cooled. as they cool, primer molecules hydrogen bond to their target sequence on the DNA<br>3. a heat-stable DNA polymerase builds new DNA strands by extending the primers the 5'&gt;3' direction<br>^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^<br>these 3 steps are repeated over and over, doubling the amount of DNA after each cycle</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:07:46 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162160138</guid>
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         <title>What enzyme does PCR use?</title>
         <author>20epetersen</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162160483</link>
         <description><![CDATA[<div>TAQ polymerase</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:08:33 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162160483</guid>
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         <title>What are &quot;sticky ends&quot;?</title>
         <author>20pcromley</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162160569</link>
         <description><![CDATA[<div>After restriction enzymes cut through DNA, the sticky ends attach to each other with the help of DNA ligase. Sticky ends fit perfectly together.</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:08:46 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162160569</guid>
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         <title>What does PCR stand for?</title>
         <author>tmtgill</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162160903</link>
         <description><![CDATA[<div>Polymerase Chain Reaction<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:09:35 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162160903</guid>
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         <title>GEL ELECTROPHORESIS</title>
         <author>20nahmad</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162160906</link>
         <description><![CDATA[<div>Why do large molecules move more slowly than smaller molecules?<br><br>Large molecules are obviously larger and bulkier so they take up more room. Small molecules do not have to stay attached to any other molecules which makes it easy for them to move more quickly while taking up less room.</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:09:35 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162160906</guid>
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         <title>What is the purpose of adding antibiotic resistance in recombinant DNA?</title>
         <author>20epetersen</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162160909</link>
         <description><![CDATA[<div>To determine whether or not bacteria picked up the plasmids</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:09:36 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162160909</guid>
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         <title>How does gel electrophoresis order DNA strands by size?</title>
         <author>20pcromley</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162161212</link>
         <description><![CDATA[<div>The smaller fragments move faster, because the larger fragments are held back by the thicket of of polymer fibers within the gel.<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:10:22 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162161212</guid>
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         <title>What was the purpose of arabinose in the pGLO lab?</title>
         <author>20epetersen</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162161441</link>
         <description><![CDATA[<div>To activate the gene that produces the glowing protein</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:10:58 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162161441</guid>
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         <title>What is the purpose of the buffer?</title>
         <author>20sfaruqi</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162161570</link>
         <description><![CDATA[<div>It is the liquid where the reaction happens.</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:11:17 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162161570</guid>
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         <title>What are the ingredients for PCR?</title>
         <author>tmtgill</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162161664</link>
         <description><![CDATA[<div>-Target DNA<br>-Primers<br>-DNA nucleotides</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:11:31 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162161664</guid>
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         <title>GEL ELECTROPHORESIS</title>
         <author>20nahmad</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162161942</link>
         <description><![CDATA[<div>Why is TAE buffer solution necessary during gel electrophoresis?<br><br>It holds the electrical current which makes things happen, thus showing visible data to the lab technician who needs it for a crime case.</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:12:10 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162161942</guid>
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         <title>What enzyme adds nucleotides?</title>
         <author>20sfaruqi</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162161982</link>
         <description><![CDATA[<div>Taq polymerase</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:12:16 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162161982</guid>
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         <title>If you needed to make a large amount of a specific segment of DNA, what method would you use?</title>
         <author>20pcromley</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162162314</link>
         <description><![CDATA[<div>A polymerase chain reaction (PCR)</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:13:07 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162162314</guid>
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         <title>TAQ</title>
         <author>tmtgill</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162162392</link>
         <description><![CDATA[<div>Thermus Aquatics</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:13:18 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162162392</guid>
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         <title>Recombinant DNA</title>
         <author>18vrana</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162162620</link>
         <description><![CDATA[<div>What happens if you cut through all the antibiotic resistants in the gene?<br><br>Answer: The plasmid would not survive because the antibiotics would kill it.<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:13:46 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162162620</guid>
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         <title>Paper plasmid lab</title>
         <author>20bdemarco</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162162757</link>
         <description><![CDATA[<div>explain the role of DNA lingase in in making recombinant DNA?<br>DNA lingase will anneal the the designated gene to the bacterial plasmid</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:14:01 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162162757</guid>
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         <title>What is DNA profiling?</title>
         <author>20pcromley</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162162914</link>
         <description><![CDATA[<div>The analysis of DNA samples to determine whether they came from the same individual.</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:14:20 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162162914</guid>
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         <title>Why must DNA from 2 different sources be cut with the same restriction enzyme?</title>
         <author>20epetersen</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162163055</link>
         <description><![CDATA[<div>To make the "sticky ends" that will allow them to be joined</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:14:37 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162163055</guid>
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         <title>GEL ELECTROPHORESIS</title>
         <author>20nahmad</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162163271</link>
         <description><![CDATA[<div>What color is the negative pole, always?<br><br>BLACK</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:15:01 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162163271</guid>
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      <item>
         <title>VOCAB</title>
         <author>20cblank</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162163530</link>
         <description><![CDATA[<div><strong>biotechnology</strong>: the manipulation of organisms or their components to make useful products<br><br><strong>DNA technology</strong>: modern laboratory techniques for studying and manipulating genetic material<br><br><strong>recombinant DNA</strong>: formed when scientists combine pieces of DNA from 2 different sources, often different species, in vitro(in a test tube) to form a single DNA molecule<br><br><strong>genetic engineering</strong>: the direct manipulation of genes for practical purposes<br><br><strong>plasmids</strong>: small circular DNA molecules that replicate separately from the larger bacterial chromosome<br><br><strong>gene cloning</strong>: the production of many identical copies of a gene carrying piece of DNA<br><br><strong>vector</strong>: gene carrier<br><br><strong>DNA ligase</strong>: joins the 2 DNA molecules by way of covalent bonds<br><br><strong>clone</strong>: group of identical cells descended from a single ancestral cell<br><br><strong>restriction enzymes</strong>: cutting tools that are bacterial enzymes<br><br><strong>restriction site</strong>: short DNA sequence in which a restriction enzyme cuts<br><br><strong>restriction fragments</strong>: yielding pieces of DNA that were cut by restriction enzymes<br><br><strong>genomic library</strong>: a collection of clone DNA fragments that include an organisms entire genome<br><br><strong>reverse transcriptase</strong>: a viral enzyme that can synthesize DNA from an RNA template<br><br><strong>complementary DNA (cDNA)</strong>: represents only the subset of genes that have been transcribed into mRNA in the starting cells. useful for studying the genes responsible for the specialized functions of a particular cell type; ex: brain or liver<br><br><strong>nucleic acid probe</strong>: used to find a specific gene or other nucleotide sequence within a mass of DNA<br><br><strong>vaccine:</strong> a harmless varient(mutant) or derivative of a pathogen usually a bacteria or virus that is used to stimulate the immune system to mount a lasting defense against that pathogen, thereby preventing disease<br><br><strong>GMOs:</strong> organisms that have acquired one or more genes by artificial means<br><br><strong>transgenic organism:</strong> if new gene is from another organism, typically of another species, the recombinant organism, is called this<br><br><strong>gene therapy:</strong> alteration of a diseased individual's genes for therapeutic purposes<br><br><strong>DNA profiling</strong>: the analysis of DNA samples to determine whether they came from the same individual<br><br><strong>polymerase chain reaction(PCR):</strong> a technique by which a specific segment of a DNA molecule can be targeted and quickly amplified in the laboratory<br><br><strong>primers:</strong> short chemically synthesized single-stranded DNA molecules with sequences that are complementary to sequences at each end of the target sequence<br><br><strong>gel electrophoresis:</strong> a method that separates macromolecules on the base of size, electrical charge, or other physical properties</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:15:31 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162163530</guid>
      </item>
      <item>
         <title>What is DNA ligase?</title>
         <author>tmtgill</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162163591</link>
         <description><![CDATA[<div>-a molecule that helps the formation of covalent bonds between nucleotides<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:15:39 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162163591</guid>
      </item>
      <item>
         <title>Gel Electrophoresis </title>
         <author>katiah711</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162163683</link>
         <description><![CDATA[<div>In Gel Electrophoresis there is a positive and negative end, in which direction does the DNA migrate?&nbsp; why?<br><br>DNA moves towards the positive end of the Gel because it is negatively charged (due to phosphate groups) so is attracted to the positive charge</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:15:52 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162163683</guid>
      </item>
      <item>
         <title>Gene Cloning Steps</title>
         <author>pattychow</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162163953</link>
         <description><![CDATA[<div>~~~~~~~~~~~~~~~~~~~~~<br>1. A plasmid is isolated<br>~~~~~~~~~~~~~~~~~~~~~<br>2. The cell's DNA is isolated<br>~~~~~~~~~~~~~~~~~~~~~<br>3. The plasmid is cut with an enzyme<br>~~~~~~~~~~~~~~~~~~~~~<br>4. The cell's DNA is cut with the same enzyme<br>~~~~~~~~~~~~~~~~~~~~~<br>5. The targeted fragment and plasmid DNA are combined<br>~~~~~~~~~~~~~~~~~~~~~<br>6. DNA ligase is added, which joins the two DNA molecules<br>~~~~~~~~~~~~~~~~~~~~~<br>7. The recombinant plasmid is taken by a bacterium through transformation<br>~~~~~~~~~~~~~~~~~~~~~<br>8. The bacterium reproduces<br>~~~~~~~~~~~~~~~~~~~~~<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:16:31 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162163953</guid>
      </item>
      <item>
         <title>DNA Technology</title>
         <author>tmtgill</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162164095</link>
         <description><![CDATA[<div>-techniques for manipulating DNA</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:16:50 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162164095</guid>
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      <item>
         <title>Why are bacteria often the best organisms for manufacturing a protein product?</title>
         <author>20pcromley</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162164247</link>
         <description><![CDATA[<div>-they can be grown rapidly and cheaply<br>-phages and plasmids are widely available for use as gene-cloning vectors<br>-they can be engineered to produce large amounts of the protein</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:17:10 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162164247</guid>
      </item>
      <item>
         <title>What do bacteria use restriction enzymes for?</title>
         <author>20epetersen</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162164283</link>
         <description><![CDATA[<div>To cut out DNA inserted into the bacterium by bacteriophages</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:17:14 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162164283</guid>
      </item>
      <item>
         <title>BIOTECHNOLOGY</title>
         <author>tmtgill</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162164383</link>
         <description><![CDATA[<div>-use of organisms or their products&nbsp; for human purposes<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:17:28 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162164383</guid>
      </item>
      <item>
         <title>Restriction Enzymes</title>
         <author>cbaekseymour</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162165135</link>
         <description><![CDATA[<div>What do restriction enzymes do against bacteriophages?<br>-Destroy the injected DNA, cutting it at places where it sees its specific DNA sequence (Restriction Site). <br>How do the restriction enzymes know to not cut the cells own DNA?<br>-Methyl groups attached to the DNA. <br>What are sticky ends?<br>-Sticky ends are ends that have been cut by the restriction enzymes and have a specific DNA sequence that pairs with another part that has been cut by the same restriction enzyme. They fit together because of their base-pairing rules.<br>What does DNA ligase do?<br>-It solidifies the bond between the sticky ends. <br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:19:16 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162165135</guid>
      </item>
      <item>
         <title>Gene Therapy Steps</title>
         <author>emmaberthiaux2020</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162165147</link>
         <description><![CDATA[<div>Alteration of a diseased individual's genes for therapeutic reasons<br><br>1. A gene from a healthy person is cloned and then converted to an RNA Version which is inserted into the RNA genome of a harmless virus&nbsp;<br>2. Bone marrow cells are taken from patient and infected with recombinant virus<br>3. The virus inserts a DNA version of its genome and a normal human gene into the cells' DNA<br>4. The engineered cells are then injected back into the patient<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:19:18 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162165147</guid>
      </item>
      <item>
         <title>PLASMID</title>
         <author>tmtgill</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162165163</link>
         <description><![CDATA[<div>-round bacterial chromosome</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:19:19 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162165163</guid>
      </item>
      <item>
         <title>What machine is used to copy DNA very quickly?</title>
         <author>20epetersen</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162165184</link>
         <description><![CDATA[<div>Thermocycler</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:19:24 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162165184</guid>
      </item>
      <item>
         <title>RECOMBINANT DNA</title>
         <author>tmtgill</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162165290</link>
         <description><![CDATA[<div>-DNA combined with two different sources</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:19:42 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162165290</guid>
      </item>
      <item>
         <title>Why is a restriction enzyme that cuts through the ORI unusbale?</title>
         <author>20sfaruqi</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162165332</link>
         <description><![CDATA[<div>because then the plasmid won't be able to replicate<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:19:48 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162165332</guid>
      </item>
      <item>
         <title>GENETIC ENGINEERING</title>
         <author>tmtgill</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162165556</link>
         <description><![CDATA[<div>-purposefully altering genes for human purposes</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:20:22 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162165556</guid>
      </item>
      <item>
         <title></title>
         <author>20pcromley</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162165826</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://padletuploads.blob.core.windows.net/prod/185501106/ef6012c42b3ce6129ca0c159d1563375/a.jpg" />
         <pubDate>2017-03-23 15:21:04 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162165826</guid>
      </item>
      <item>
         <title>Nucleic Acid Probe</title>
         <author>cbaekseymour</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162165968</link>
         <description><![CDATA[<div>What is the purpose of the Nucleic Acid Probe?<br>-It allows researchers to find their gene of interest. It has a complimentary base-pairing to the gene of interest.</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:21:23 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162165968</guid>
      </item>
      <item>
         <title>What unique property of DNA allows two distinct samples of DNA to bind at &quot;sticky&#39;&#39; ends?</title>
         <author>20sfaruqi</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162166181</link>
         <description><![CDATA[<div>The base pairing Rule</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:21:55 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162166181</guid>
      </item>
      <item>
         <title>gel electrophoresis</title>
         <author>20pcromley</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162166567</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://padletuploads.blob.core.windows.net/prod/185501106/87da425d4e38792f43948b8369fe028c/b.gif" />
         <pubDate>2017-03-23 15:22:43 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162166567</guid>
      </item>
      <item>
         <title>GENOMIC LIBRARY</title>
         <author>tmtgill</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162166797</link>
         <description><![CDATA[<div>-entire collection of cloned DNA pieces that consist of an organism's genome </div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:23:11 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162166797</guid>
      </item>
      <item>
         <title>PCR</title>
         <author>20epetersen</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162166914</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://padletuploads.blob.core.windows.net/prod/185501138/6ffb4c7884c660a79594cf1c86ed4160/Screen_Shot_2017_03_23_at_10_22_36_AM.png" />
         <pubDate>2017-03-23 15:23:27 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162166914</guid>
      </item>
      <item>
         <title>Recombinant DNA</title>
         <author>18vrana</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162167197</link>
         <description><![CDATA[<div>How many antibiotic resistants do you need to make a function recombinant DNA?<br><br>Answer: At least one.</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:24:04 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162167197</guid>
      </item>
      <item>
         <title>GENE THERAPY</title>
         <author>tmtgill</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162167595</link>
         <description><![CDATA[<div>-the replacement of a person's disease-causing genes with functioning genes</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:25:00 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162167595</guid>
      </item>
      <item>
         <title>Reverse Transcription</title>
         <author>20epetersen</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162167922</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://padletuploads.blob.core.windows.net/prod/185501138/37a7d5bfaad1b173364dc360d04a7e65/Screen_Shot_2017_03_23_at_10_25_23_AM.png" />
         <pubDate>2017-03-23 15:25:56 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162167922</guid>
      </item>
      <item>
         <title>What happens in a bacterial cell during transformation?</title>
         <author>tmtgill</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162168588</link>
         <description><![CDATA[<div>-once the plasmid is within the bacterium, protein synthesis begins<br>-beta-lactamase is produced and provides resistance to ampicillin<br>-if arabinose is present, then GFP is also produced</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:27:28 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162168588</guid>
      </item>
      <item>
         <title>Primers</title>
         <author>cbaekseymour</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162169275</link>
         <description><![CDATA[<div>What is a primer?<br>-Short, artificially created, single strands of DNA that bind to each end of a target sequence in a PCR procedure. Usually 15-20 nucleotides long .</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:29:07 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162169275</guid>
      </item>
      <item>
         <title>link to a practice test</title>
         <author>20pcromley</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162170018</link>
         <description><![CDATA[<div><a href="http://wps.aw.com/bc_campbell_concepts_7_oa/215/55141/14116147.cw/index.html">http://wps.aw.com/bc_campbell_concepts_7_oa/215/55141/14116147.cw/index.html</a></div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:30:37 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162170018</guid>
      </item>
      <item>
         <title>link to a quizlet</title>
         <author>annieperugini</author>
         <link>https://padlet.com/tinadavies03/w0gziocwm913/wish/162170828</link>
         <description><![CDATA[<div><a href="https://quizlet.com/112400724/biotechnology-flash-cards/">https://quizlet.com/112400724/biotechnology-flash-cards/</a></div>]]></description>
         <enclosure url="" />
         <pubDate>2017-03-23 15:32:29 UTC</pubDate>
         <guid>https://padlet.com/tinadavies03/w0gziocwm913/wish/162170828</guid>
      </item>
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