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  <id>http://groups.google.com/group/bionet.organisms.zebrafish</id>
  <title type="text">bionet.organisms.zebrafish Google Group</title>
  <subtitle type="text">
  Research on Zebrafish (Daniorerio) (Moderated)
  </subtitle>
  <link href="/group/bionet.organisms.zebrafish/feed/atom_v1_0_msgs.xml" rel="self" title="bionet.organisms.zebrafish feed"/>
  <updated>2013-06-06T07:18:08Z</updated>
  <generator uri="http://groups.google.com" version="1.99">Google Groups</generator>
  <entry>
  <author>
  <name>Michael Brand</name>
  <email>michael.br...@biotec.tu-dresden.de</email>
  </author>
  <updated>2013-06-06T07:18:08Z</updated>
  <id>http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/731a8e42600be8f4/26ff23fa9184dc42?show_docid=26ff23fa9184dc42</id>
  <link href="http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/731a8e42600be8f4/26ff23fa9184dc42?show_docid=26ff23fa9184dc42"/>
  <title type="text">amyloids, NFTs or Lewy body protocol?</title>
  <summary type="html" xml:space="preserve">
  Dear colleagues &lt;br&gt; &lt;p&gt;has anyone had any luck with a staining protocol to detect amyloid deposits, neurofibrillary tangles (NFTs) or Lewy bodies in zebrafish brain ? I would be grateful for some help. &lt;br&gt; &lt;p&gt;best wishes &lt;br&gt; &lt;p&gt;Michael Brand &lt;br&gt; Dresden
  </summary>
  </entry>
  <entry>
  <author>
  <name>KerryGirleen</name>
  <email>miriam_moria...@hotmail.com</email>
  </author>
  <updated>2013-05-22T13:41:26Z</updated>
  <id>http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/0b44528a9cbcda9b/73c81fa91add24e4?show_docid=73c81fa91add24e4</id>
  <link href="http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/0b44528a9cbcda9b/73c81fa91add24e4?show_docid=73c81fa91add24e4"/>
  <title type="text">Re: [Zbrafish] pCS2Tal3 target vectors</title>
  <summary type="html" xml:space="preserve">
  Hi Richard &lt;br&gt; &lt;p&gt;Thanks for clearing that up for me! &lt;br&gt; &lt;p&gt;Miriam
  </summary>
  </entry>
  <entry>
  <author>
  <name>Richard Maguire</name>
  <email>richard.magu...@york.ac.uk</email>
  </author>
  <updated>2013-05-09T08:47:48Z</updated>
  <id>http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/0b44528a9cbcda9b/c5a03acba5f1edc2?show_docid=c5a03acba5f1edc2</id>
  <link href="http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/0b44528a9cbcda9b/c5a03acba5f1edc2?show_docid=c5a03acba5f1edc2"/>
  <title type="text">Re: [Zbrafish] pCS2Tal3 target vectors</title>
  <summary type="html" xml:space="preserve">
  Hi, Miriam. &lt;br&gt; &lt;p&gt;The Grunwald lab pCS2 TAL3 destination vectors use obligate &lt;br&gt; heterodimeric FOKI domains. DD must heterodimerise with RR in order to &lt;br&gt; induce a double strand break. This reduces possible off target effects &lt;br&gt; you may otherwise get due to spurious homodimerisation of the &amp;quot;standard&amp;quot; &lt;br&gt; homodimeric FokI.
  </summary>
  </entry>
  <entry>
  <author>
  <name>KerryGirleen</name>
  <email>miriam_moria...@hotmail.com</email>
  </author>
  <updated>2013-05-08T15:18:51Z</updated>
  <id>http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/0b44528a9cbcda9b/a6fe97ea5d7d7185?show_docid=a6fe97ea5d7d7185</id>
  <link href="http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/0b44528a9cbcda9b/a6fe97ea5d7d7185?show_docid=a6fe97ea5d7d7185"/>
  <title type="text">pCS2Tal3 target vectors</title>
  <summary type="html" xml:space="preserve">
  Hi all &lt;br&gt; &lt;p&gt;I&#39;m looking to use pCS2Tal3 as my final target vector for my TALENs &lt;br&gt; but I&#39;ve found that there are two mentioned in most protocols and on &lt;br&gt; the ADDGENE website: &lt;br&gt; &lt;p&gt;pCS2TAL3DD and pCS2TAL3RR. &lt;br&gt; &lt;p&gt;Does it matter which one I use? Can I use the same one for my forward &lt;br&gt; and reverse monomers or do I need to use both? If not which one would
  </summary>
  </entry>
  <entry>
  <author>
  <email>htomasiew...@gmail.com</email>
  </author>
  <updated>2013-05-03T19:40:54Z</updated>
  <id>http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/7a88af7ec7eacbd7/3ce171bbc06b6c40?show_docid=3ce171bbc06b6c40</id>
  <link href="http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/7a88af7ec7eacbd7/3ce171bbc06b6c40?show_docid=3ce171bbc06b6c40"/>
  <title type="text">Re: Funduscopy zebrafish</title>
  <summary type="html" xml:space="preserve">
  In addition to the melanin in the retina older fish will have a shiny reflective layer made up of the iridiphores. We have a line of fish, sheer, which lacks these pigments. For younger fish you may be able to use albinos.
  </summary>
  </entry>
  <entry>
  <author>
  <name>Tyrone Genade</name>
  <email>tgen...@gmail.com</email>
  </author>
  <updated>2013-04-30T10:34:51Z</updated>
  <id>http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/8866c08de88db1df/cfa1961a4209ebd2?show_docid=cfa1961a4209ebd2</id>
  <link href="http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/8866c08de88db1df/cfa1961a4209ebd2?show_docid=cfa1961a4209ebd2"/>
  <title type="text">Re: Zbrafish Digest, Vol 93, Issue 3</title>
  <summary type="html" xml:space="preserve">
  did it work?
  </summary>
  </entry>
  <entry>
  <author>
  <name>David Lains</name>
  <email>davidla...@gmail.com</email>
  </author>
  <updated>2013-04-11T18:20:58Z</updated>
  <id>http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/c3fba6858f3120ba/4f96ea276d0118ef?show_docid=4f96ea276d0118ef</id>
  <link href="http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/c3fba6858f3120ba/4f96ea276d0118ef?show_docid=4f96ea276d0118ef"/>
  <title type="text">Re: roy mutant line</title>
  <summary type="html" xml:space="preserve">
  Hello Will &lt;br&gt; &lt;p&gt;ZIRC has the Roy as a single line in the freezers so the recovered embryos would be het/wildtype. &lt;br&gt; &lt;a target=&quot;_blank&quot; rel=nofollow href=&quot;http://zebrafish.org/zirc/fish/lineAll.php?t=Anything&amp;c=ZL1675&amp;searchMenuQuick=Go&quot;&gt;[link]&lt;/a&gt; &lt;br&gt; &lt;p&gt;We also have the Roy in a double mutant with nacre in the transparent casper line. &lt;br&gt; &lt;a target=&quot;_blank&quot; rel=nofollow href=&quot;http://zebrafish.org/zirc/fish/lineAll.php?t=Anything&amp;c=ZL1714&amp;searchMenuQuick=Go&quot;&gt;[link]&lt;/a&gt;
  </summary>
  </entry>
  <entry>
  <author>
  <email>j...@silvaggi.com</email>
  </author>
  <updated>2013-04-11T02:09:09Z</updated>
  <id>http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/7fee389ba8845807/c735577c5401801d?show_docid=c735577c5401801d</id>
  <link href="http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/7fee389ba8845807/c735577c5401801d?show_docid=c735577c5401801d"/>
  <title type="text">Sheer Zebrafish available through MTA</title>
  <summary type="html" xml:space="preserve">
  Dear All, &lt;br&gt; &lt;p&gt;I wanted to inform you of a very useful zebrafish model developed at the University of Wisconsin-Milwaukee by Dr. Henry Tomasiewicz. This triple homozygous mutant fish, known as sheer zebrafish, are characterized by their optically transparent quality throughout life. His laboratory has crossed mutants transparent (tra), albino (alb), and pfeffer (pfe) in which homozygous mutants are each defective in synthesis of different pigments (iridophores, melanin, and xanthophores respectively). Transparent zebrafish enable studies requiring the observation of cellular processes and interactions, and allow for manipulation of cells in adult fish. Sheer fish also allow for observation of all of the internal organs in the adult fish. These transparent fish are ideal for the study of fluorescent proteins, especially when studying the effects of environmental toxicants on neurodegenerative and other disease processes where optical clarity is at a premium.
  </summary>
  </entry>
  <entry>
  <author>
  <name>Will Norton</name>
  <email>wnm...@gmail.com</email>
  </author>
  <updated>2013-04-11T13:17:31Z</updated>
  <id>http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/c3fba6858f3120ba/3448b30d1a2c8d72?show_docid=3448b30d1a2c8d72</id>
  <link href="http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/c3fba6858f3120ba/3448b30d1a2c8d72?show_docid=3448b30d1a2c8d72"/>
  <title type="text">roy mutant line</title>
  <summary type="html" xml:space="preserve">
  HI everyone &lt;br&gt; &lt;p&gt;I am trying to track down the roy mutant line, which I need to do some behavioural experiments. &lt;br&gt; &lt;p&gt;Does anyone have it swimming around in their aquarium who would be willing to send it to me? &lt;br&gt; &lt;p&gt;Thanks &lt;br&gt; &lt;p&gt;Will
  </summary>
  </entry>
  <entry>
  <author>
  <name>Patrick Mueller</name>
  <email>patrick.muel...@tuebingen.mpg.de</email>
  </author>
  <updated>2013-04-06T15:27:05Z</updated>
  <id>http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/b9308d7fc32026b4/bc3076e8e41d5ac0?show_docid=bc3076e8e41d5ac0</id>
  <link href="http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/b9308d7fc32026b4/bc3076e8e41d5ac0?show_docid=bc3076e8e41d5ac0"/>
  <title type="text">open positions in Tübingen, Germany</title>
  <summary type="html" xml:space="preserve">
  Dear zebrafish researchers, &lt;br&gt; &lt;p&gt;Ph.D. and postdoctoral positions are available in my lab at the Max &lt;br&gt; Planck Institute for Developmental Biology in Tï¿œbingen, Germany. &lt;br&gt; &lt;p&gt;We study classical developmental biology questions with quantitative &lt;br&gt; methods in zebrafish embryos. We want to understand how extracellular
  </summary>
  </entry>
  <entry>
  <author>
  <name>zebrafish</name>
  <email>ap...@zebrafish.org</email>
  </author>
  <updated>2013-04-02T23:44:15Z</updated>
  <id>http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/6bcc1fa567ea0494/1cd3e968253b5c32?show_docid=1cd3e968253b5c32</id>
  <link href="http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/6bcc1fa567ea0494/1cd3e968253b5c32?show_docid=1cd3e968253b5c32"/>
  <title type="text">Re: paramecium filters</title>
  <summary type="html" xml:space="preserve">
  Hi Claudia and Aaron, &lt;br&gt; The original sizes may not be available, so I recommend using 100 micron and 20 or 10 mircon. When searching the web, look for &#39;bolting cloth&#39;. The following website has several sizes: &lt;br&gt; &lt;p&gt;&lt;a target=&quot;_blank&quot; rel=nofollow href=&quot;http://www.wildco.com/Nitex_Bolting_Cloth.html&quot;&gt;[link]&lt;/a&gt; &lt;br&gt; &lt;p&gt;Additional note, ZIRC has an updated paramecia culturing protocol on-line if you haven&#39;t seen it. I would be happy to answer questions, if needed.
  </summary>
  </entry>
  <entry>
  <author>
  <name>zebrafish</name>
  <email>ap...@zebrafish.org</email>
  </author>
  <updated>2013-04-02T23:44:15Z</updated>
  <id>http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/6bcc1fa567ea0494/ef9445a9a755d1d5?show_docid=ef9445a9a755d1d5</id>
  <link href="http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/6bcc1fa567ea0494/ef9445a9a755d1d5?show_docid=ef9445a9a755d1d5"/>
  <title type="text">Re: paramecium filters</title>
  <summary type="html" xml:space="preserve">
  Hi Claudia and Aaron, &lt;br&gt; The original sizes may not be available, so I recommend using 100 micron and 20 or 10 mircon. When searching the web, look for &#39;bolting cloth&#39;. The following website has several sizes: &lt;br&gt; &lt;p&gt;&lt;a target=&quot;_blank&quot; rel=nofollow href=&quot;http://www.wildco.com/Nitex_Bolting_Cloth.html&quot;&gt;[link]&lt;/a&gt; &lt;br&gt; &lt;p&gt;Additional note, ZIRC has an updated paramecia culturing protocol on-line if you haven&#39;t seen it. I would be happy to answer questions, if needed.
  </summary>
  </entry>
  <entry>
  <author>
  <email>amlam...@gmail.com</email>
  </author>
  <updated>2013-04-02T15:47:57Z</updated>
  <id>http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/6bcc1fa567ea0494/8fd8726d4a7f690b?show_docid=8fd8726d4a7f690b</id>
  <link href="http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/6bcc1fa567ea0494/8fd8726d4a7f690b?show_docid=8fd8726d4a7f690b"/>
  <title type="text">Re: paramecium filters</title>
  <summary type="html" xml:space="preserve">
  I am looking for the same filter cloth for filtering paramecia. Do you have a recommendation of a vendor from which I could purchase sufficient filter cloth? &lt;br&gt; &lt;p&gt;Thanks, &lt;br&gt; Aaron
  </summary>
  </entry>
  <entry>
  <author>
  <name>KdeLinde</name>
  <email>k.deli...@gmail.com</email>
  </author>
  <updated>2013-04-02T06:21:21Z</updated>
  <id>http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/1cb1f04808f332ad/f54df55de9708f01?show_docid=f54df55de9708f01</id>
  <link href="http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/1cb1f04808f332ad/f54df55de9708f01?show_docid=f54df55de9708f01"/>
  <title type="text">Post doc position in developmental genetics - in Copenhagen</title>
  <summary type="html" xml:space="preserve">
  Post doc in developmental genetics &lt;br&gt; Vacant position as Post doc in developmental genetics (around 3 years) at Department of Cellular and Molecular Medicine, Faculty of Health and Medical Sciences, University of Copenhagen &lt;br&gt; &lt;p&gt;Our research group focuses on molecular genetics of cardiac development and congenital heart disease (CHD). The post doc project will span from identification of disease genes in patients with heart defects to investigations of molecular mechanisms involved in heart development - with focus on left-right patterning. Functional characterization of cardiac developmental genes will be performed using the zebrafish as a model organism, and the project will include implementation of methods in zebrafish for gene targeting (e.g. TALENs) and phenotypic characterization of heart defects. Thus, we exclusively seek candidates with documented expertise in zebrafish developmental biology.
  </summary>
  </entry>
  <entry>
  <author>
  <name>Jenny Lenkowski</name>
  <email>jle...@umich.edu</email>
  </author>
  <updated>2013-03-26T17:12:24Z</updated>
  <id>http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/1ed4df80bb7d6e9d/7053e1783b44a146?show_docid=7053e1783b44a146</id>
  <link href="http://groups.google.com/group/bionet.organisms.zebrafish/browse_thread/thread/1ed4df80bb7d6e9d/7053e1783b44a146?show_docid=7053e1783b44a146"/>
  <title type="text">Re: protocol</title>
  <summary type="html" xml:space="preserve">
  Hi Beth, &lt;br&gt; &lt;p&gt;We started using an alkaline lysis protocol that is quick and a lot cheaper than a proteinase K digestion. I have copied it below. We have also successfully used this for genotyping whole embryos, just with smaller volumes. &lt;br&gt; &lt;p&gt;Best, &lt;br&gt; Jenny &lt;br&gt; Post-doctoral Fellow, Raymond Lab &lt;br&gt; University of Michigan
  </summary>
  </entry>
</feed>
