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<title>bionet.genome.arabidopsis</title>
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<description>Posts for bionet.genome.arabidopsis</description>
<lastBuildDate>Mon, 22 Sep 2008 14:39:31 PDT</lastBuildDate>
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	<title><![CDATA[Sourcing FM4-64]]></title>
	<guid>http://www.nnseek.com/e/bionet.genome.arabidopsis/sourcing_fm4_64_102595570t.html</guid>
	<link>http://www.nnseek.com/e/bionet.genome.arabidopsis/sourcing_fm4_64_102595570t.html</link>
	<description><![CDATA[Hello!<br><br>I am looking into buying FM4-64 to stain cell membranes in living<br>Arabidopsis shoots.  I see that i can buy 1 mg of FM4-64 from<br>Invitrogen/Molecular Probes for about $400 (CAD.)  I've also found a<br>second supplier, Calbiochem, that sells FM4-64 under the name<br>SynaptoRed for $240 (CAD) for 5 mg.  The publications i've looked at<br>have all used FM4-64 from Molecular Probes.  I'm wondering if anyone<br>has used Calbiochem's SynaptoRed/FM4-64 in Arabidopsis, and if they<br>could comment on it's efficacy at staining cell membranes.<br><br>Thanks very much,<br><br>danielle<br><br>
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	<pubDate>Mon, 22 Sep 2008 14:39:31 PDT</pubDate>
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	<title><![CDATA[Post Doctoral Positions in Plant Molecular Biology]]></title>
	<guid>http://www.nnseek.com/e/bionet.genome.arabidopsis/post_doctoral_positions_in_plant_molecular_biology_102437874t.html</guid>
	<link>http://www.nnseek.com/e/bionet.genome.arabidopsis/post_doctoral_positions_in_plant_molecular_biology_102437874t.html</link>
	<description><![CDATA[POST DOCTORAL POSITIONS IN PLANT MOLECULAR BIOLOGY IN THE UNIVERSITY OF<br>MELBOURNE AUSTRALIA<br><br><br><br>Expressions of interest are sought to fill postdoctoral positions within the<br>Plant Molecular Biology and Biotechnology group, at the Melbourne School of<br>Land and Environment at The University of Melbourne, highest ranked Research<br>University in Australia.   We are interested in recruiting highly motivated<br>individuals with a desire to succeed and contribute to the internationally<br>competitive research activities of the laboratory focussing on molecular<br>mechanisms of differentiation and cell specific gene regulation during<br>meristem development, floral transition and reproductive differentiation. A<br>brief description of research projects is provided below.<br> <br>MicroRNAs and Epigenetic Regulation of Meristem Development<br> <br>MicroRNAs (miRNAs) are small non-coding RNAs that regulate expression of<br>many genes.  We have recently discovered a network of shoot apical meristem<br>specific miRNAs. These include novel plant miRNAs being reported for the<br>first time.  The postdoctoral research project will involve investigation of<br>role of these novel miRNAs in meristem development and floral transition<br>using computational and experimental tools.  The experimental approach will<br>include expression profiling of individual miRNAs through gel blots,<br>microarrays, in situ localizations combined with gain-and loss-of-function<br>studies in transgenic plants.<br> <br>Molecular Control of Stem Cell Maintenance in Plants<br> <br>Shoot apical meristems (SAMs) provide niches for self-sustaining groups of<br>stem cells that play a critical role in plant development being founder<br>cells of all aerial plant parts.  Maintenance of these stem cells is thus<br>essential for repetitive organ initiation throughout plant lifecycle.  Using<br>high throughput gene expression profiling technologies we have identified<br>subset of novel genes that are differentially expressed in shoot apical<br>meristem of pea and soybeans.  The postdoctoral appointee will participate<br>in a project addressing developmental role of these genes.  The approaches<br>will include laser capture microdissection, mutant analyses, in situ<br>hybridisations, and reporter gene expression and gain-and loss-of-function<br>studies in transgenic plants.<br> <br>Male Germ Line Development and Fertilization in Flowering Plants<br> <br>Unlike animals where germ line cells diverge from somatic cells during early<br>embryo development the plant germ lineages initiate late in development at<br>flowering stage.  The male germline in plants begins with an asymmetric<br>division, after which one of the resulting cells, the generative cell,<br>divides symmetrically to produce two sperm cells. Research from our<br>laboratory has revealed that the male germ line cells show transcriptional<br>repertoire that is highly divergent from other reproductive and somatic<br>cells.  The post-doctoral appointee will participate in a project focusing<br>on role of cell specific genes and nature of associated regulatory<br>mechanisms. Potential approaches include Potential approaches include<br>DNA-protein interaction analyses, chromatin immunoprecipitation (ChiP), gene<br>knockout in transgenic plants, proteome and methylome analysis,<br>live imaging of fertilization events.<br> <br>Applicants should possess a PhD, together with relevant experience in one or<br>more fields of functional genomics, molecular genetics and cell biology and<br>be able to provide evidence of proven research productivity in the form of<br>publications in refereed journals. Candidates should also be experienced in<br>general molecular biology techniques and ideally have expertise in one or<br>more of following techniques/approaches; protein-DNA interactions,<br>protein-protein interactions, ChIP, protein biochemistry and bioinformatics.<br> <br>The positions are being offered at Research Fellow ( Level A) position with<br>salary range of $63,451-$68,109 p.a.  Candidates with exceptional<br>achievements can be considered for appointment at a higher salary level.<br>Applications close on 17 th October 2008.  For further details contact:<br>Professor Prem L Bhalla, tel. +61 3 8344 9651, email premlb@<a href="http://unimelb.edu.au" rel="nofollow" class="url" target="_blank">unimelb.edu.au</a><br>or Professor Mohan B Singh, tel. +61 3 8344 5051, email mohan@<a href="http://unimelb.edu.au" rel="nofollow" class="url" target="_blank">unimelb.edu.au</a><br><br>
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	<pubDate>Sun, 21 Sep 2008 06:57:50 PDT</pubDate>
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	<title><![CDATA[Post-doc position in Cell Biology at IJPB (Versailles, France)]]></title>
	<guid>http://www.nnseek.com/e/bionet.genome.arabidopsis/post_doc_position_in_cell_biology_at_ijpb_versailles_102029554t.html</guid>
	<link>http://www.nnseek.com/e/bionet.genome.arabidopsis/post_doc_position_in_cell_biology_at_ijpb_versailles_102029554t.html</link>
	<description><![CDATA[POST-DOCTORAL POSITION<br>IJPB, Versailles, France<br><br>Recent results obtained in our group on the characterization of the  <br>TON1, FASS/TON2 proteins and their partners uncovered converging  <br>evidences pointing towards evolutionary conservation of some  <br>centrosomal components at the plant cell's cortex. TON1 and FASS  <br>themselves are related to proteins recently shown to localize at the  <br>centrosome in animal cells. TON1 interacts with centrin, a key  <br>component of eucaryotic MTOCs. Moreover, several TON1 and FASS  <br>interactants belong to a new family of cytoskeleton-associated  <br>proteins called TIM which are reminiscent of some animal centrosomal  <br>proteins. These are the first indications ever for a functional and  <br>evolutionary link between animal centrosomes and the cortical  <br>cytoskeleton of plants, apart from gamma-tubulin dependent nucleation.  <br>Through a collaboration between our group and the group of Marilyn  <br>Vantard the successful candidate will work on the functional  <br>characterization of TON1 and TIM proteins in plant cells, and of their  <br>other interacting partners in the cell from a cytological, molecular  <br>genetics and biochemical point of view.<br><br>The position is available for candidates with outstanding academic  <br>record and excellent experimental and communication skills. It is  <br>located in Versailles (France) for 30 months, starting January 2009.  <br>Part of the work will be done in Grenoble, in Marilyn Vantard's group.  <br>Salary is 2200-2500 euros per month.<br><br>Requirements : Candidates must have a PhD with an excellent academic  <br>record. We are seeking individuals with a strong background in  <br>genetics, molecular biology, biochemistry and microscopy. Experience  <br>in protein biochemistry and/or with fluorescent protein detection and  <br>confocal laser scanning microscopy is a plus. Experience in plant  <br>biology and knowledge of the French language are not mandatory.<br><br>Application : Please send cover letter, CV, publication reprints  and  <br>names and e-mail addresses of three references to David Bouchez (bouchez@versailles.inra.fr <br>). The successful candidate will start in January 2009 or soon after.<br><br>Relevant publications :<br>	Azimzadeh et al (2008). Arabidopsis TONNEAU1 proteins are essential  <br>for preprophase band formation  and interact with centrin. Plant Cell,  <br>in press<br>	Pastuglia & Bouchez (2007). Molecular encounters at microtubule ends  <br>in the plant cell cortex. Curr Op Plant Biol 10:1-7<br>	Pastuglia et al (2006). Gamma-tubulin is essential for microtubule  <br>organization and development in Arabidopsis. Plant Cell 18 : 1412-1425<br>	Camilleri et al (2002). The Arabidopsis TONNEAU2 gene encodes a  <br>putative novel PP2A regulatory subunit essential for the control of  <br>cortical cytoskeleton. Plant Cell, 14 : 833-845.<br><br>The Jean-Pierre Bourgin Institute hosts 25 research groups devoted to  <br>plant biology, totalizing 330 people, comprised of 230 permanent staff  <br>and 100 post-docs, PhD students and others students. The IJPB has a  <br>long-standing and respected expertise in the field of plant biology,  <br>including genomics, genetics, breeding, metabolism, cell biology and  <br>development. All tools and resources relevant for integrative plant  <br>biology are available on site. Local facilities in Versailles include  <br>outstanding experimental facilities dedicated to plant culture (4500  <br>m2 glasshouses and 500 m2 controlled environment rooms), state of the  <br>art technical platforms for Microscopy and Cytology (4 confocal  <br>microscopes, classical microscopy, etc), Protein Biochemistry  <br>(electrophoresis, chromatography, MALDI-TOF MS…), Chemistry (FT-IR,  <br>several mass spec including GC-TOF and LC-MS/MS…), and Bioinformatics.<br><br>Further details and information : bouchez@versailles.inra.fr<br><br><br>David Bouchez<br>Institut Jean-Pierre Bourgin<br>Station de Génétique et Amélioration des Plantes<br>INRA Centre de Versailles - 78026 Versailles Cedex France<br>tel : +33 (0)1 30 83 33 94 - fax : +33 (0)1 30 83 33 19<br>e-mail : bouchez@versailles.inra.fr<br><a href="http://www-ijpb.versailles.inra.fr" rel="nofollow" class="url" target="_blank">http://www-ijpb.versailles.inra.fr</a><br><br>cytoskeleton group :<br><a href="http://www-ijpb.versailles.inra.fr/en/sgap/equipes/cyto" rel="nofollow" class="url" target="_blank">http://www-ijpb.versailles.inra.fr/en/sgap/equipes/cyto</a>/<br><br><br><br><br><br><br>
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        <td><a href="http://www.nnseek.com/e/bionet.genome.arabidopsis/post_doc_position_in_cell_biology_at_ijpb_versailles_102029554t.html">no comments</a></td>
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	<pubDate>Wed, 17 Sep 2008 06:06:29 PDT</pubDate>
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	<title><![CDATA[Arabidopsis Conference Survey Summary]]></title>
	<guid>http://www.nnseek.com/e/bionet.genome.arabidopsis/arabidopsis_conference_survey_summary_101437426t.html</guid>
	<link>http://www.nnseek.com/e/bionet.genome.arabidopsis/arabidopsis_conference_survey_summary_101437426t.html</link>
	<description><![CDATA[<br>If you are interested in seeing a summary of responses to the Arabidopsis<br>conference survey please see:<br><a href="http://www.arabidopsis.org/portals/masc/journal.jsp" rel="nofollow" class="url" target="_blank">http://www.arabidopsis.org/portals/masc/journal.jsp</a>#survey08<br><br>
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        <td><a href="http://www.nnseek.com/e/bionet.genome.arabidopsis/arabidopsis_conference_survey_summary_101437426t.html">no comments</a></td>
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	<pubDate>Thu, 11 Sep 2008 17:36:02 PDT</pubDate>
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	<title><![CDATA[9th IPMB Congress, St. Louis, MO, Oct 25-30, 2009]]></title>
	<guid>http://www.nnseek.com/e/bionet.genome.arabidopsis/_9th_ipmb_congress_st_louis_mo_oct_25_30_2009_101436914t.html</guid>
	<link>http://www.nnseek.com/e/bionet.genome.arabidopsis/_9th_ipmb_congress_st_louis_mo_oct_25_30_2009_101436914t.html</link>
	<description><![CDATA[Dear Colleague:<br><br>You are invited to attend the 9th International Congress of<br>Plant Molecular Biology (IPMB), October 25-30, 2009 taking place<br>in St. Louis, Missouri.  Please look at the following website for<br>all necessary information on this Congress which is composed of<br>53 symposia and 9 Plenary Lectures on all aspects of plant<br>molecular biology.<br><br>          <a href="http://www.ipmb2009.org" rel="nofollow" class="url" target="_blank">http://www.ipmb2009.org</a><br><br>Sincerely,<br><br>Perry Gustafson - Chair IPMB 2009<br>--------------------------------------------------------------------------<br>9th International Congress of Plant Molecular Biology, October 25-30, 2009<br>--------------------------------------------------------------------------<br>[Apologies, the URL sent from a previous message has been corrected here.]<br><br>
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	<pubDate>Thu, 11 Sep 2008 11:41:03 PDT</pubDate>
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	<title><![CDATA[methods for rescue T-DNA in transformants]]></title>
	<guid>http://www.nnseek.com/e/bionet.genome.arabidopsis/methods_for_rescue_t_dna_in_transformants_101437682t.html</guid>
	<link>http://www.nnseek.com/e/bionet.genome.arabidopsis/methods_for_rescue_t_dna_in_transformants_101437682t.html</link>
	<description><![CDATA[Dear all,<br><br>I am trying to rescue the T-DNA  insertion and try to know the sequence which is flanking the  T-DNA left or right border in the plant transformants. The transformed plants have a big genome. Now I try to find a very useful method to know the insertion site in the plant genome.<br><br>Do you know any methods  or have any experiences or suggestions in how to rescue / recover the T-DNA insertion? Could you let me know?<br><br>please email me: xwwang@<a href="http://uga.edu" rel="nofollow" class="url" target="_blank">uga.edu</a> <br><br>Thanks<br><br>xuewen<br><br>
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        <td><a href="http://www.nnseek.com/e/bionet.genome.arabidopsis/methods_for_rescue_t_dna_in_transformants_101437682t.html">no comments</a></td>
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	<pubDate>Thu, 11 Sep 2008 08:12:56 PDT</pubDate>
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	<title><![CDATA[Bioinformatics Analyst Position]]></title>
	<guid>http://www.nnseek.com/e/bionet.genome.arabidopsis/bioinformatics_analyst_position_101436658t.html</guid>
	<link>http://www.nnseek.com/e/bionet.genome.arabidopsis/bioinformatics_analyst_position_101436658t.html</link>
	<description><![CDATA[I realize that Medicago is not Arabidopsis, but it is another model<br>organism. You might be interested in this.<br><br> <br><br>Bioinformatics Analyst<br><br>Requisition Code:<br><br>PLAN688<br><br>Location:<br><br>Rockville, Maryland<br><br>Department:<br><br>Plant Genomics<br><br>Schedule:<br><br>Full Time<br><br> <br><br> <br><br>Job Responsibilities: The Bioinformatics Analyst will work on the<br>curation and annotation of the M. truncatula genome sequence.<br>Responsibilities will include design and maintenance of web pages<br>providing access to Medicago genome sequence and annotation and<br>associated data, including outreach to the users through a community<br>annotation portal. The ideal candidate will have hands-on research<br>experience in Medicago genomics and demonstrated competence in<br>bioinformatics including Perl, SQL, HTML and cgi-scripting. <br><br>Qualifications: Successful candidates will have a Bachelor's or Master's<br>degree in the Biological Sciences, plus experience working with<br>computers in the field of biological sciences and a familiarity with DNA<br>sequence and annotation tools and practices. Candidates will also have a<br>demonstrated competence in appropriate computer languages including<br>Perl, SQL, HTML and cgi-scripting; web technologies including HTML,<br>DHTML, XML, CSS; Graphics tools including Photoshop, Fireworks or<br>similar; Operating Systems including UNIX and UNIX variants, Windows,<br>and/or Macintosh; Relational Database including knowledge of Sybase and<br>SQL. The Bioinformatics Analyst will have a solid knowledge of molecular<br>biology as it relates to DNA sequences, sequencing technologies and<br>genomics. Strong written and verbal communication skills, excellent<br>organization and time management skills, ability to meet schedules, the<br>ability to collaborate across a multi-disciplinary team, and work<br>independently is a must.<br><br> <br><br>You can apply through the JCVI web site; the position is listed under<br>Plant Genomics.<br><br><a href="https://careers.jcvi.org/careers" rel="nofollow" class="url" target="_blank">https://careers.jcvi.org/careers</a>/<br><br> <br><br>___________________________<br><br>Chris Town<br><br>Investigator<br><br>The J. Craig Venter Institute<br><br>9704 Medical Center Drive<br><br>Rockville, MD 20850<br><br>Office Phone: 301-795-7523<br><br>Fax: 301-838-0208<br><br>Home Phone: 301-990-0878<br><br>Cell Phone: 301-204-6300<br><br> <br><br>
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	<pubDate>Thu, 11 Sep 2008 02:43:55 PDT</pubDate>
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	<title><![CDATA[problem in pcr]]></title>
	<guid>http://www.nnseek.com/e/bionet.genome.arabidopsis/problem_in_pcr_101260786t.html</guid>
	<link>http://www.nnseek.com/e/bionet.genome.arabidopsis/problem_in_pcr_101260786t.html</link>
	<description><![CDATA[i am working on tomato disease resistant gene screening i.e MAS( marker<br>assisted selection) . i have did the DNA isolation from<br>green house plant and open field plant. and complete the pcr for diffent<br>resistant gene. for near about 1500 sample the pcr is working fine got the<br>good amplification, but when i have again collected the samples after 30 day<br>the DNA Quality looks good on gel ,but not get amplified in pcr reaction. we<br>are tried the things but its not working. i would be thankful if some one<br>suggest me to over come the problem.<br><br>lookinforward for suggestion<br><br><br>With Regards<br><br>Rupesh<br>
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	<pubDate>Tue, 09 Sep 2008 23:43:37 PDT</pubDate>
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	<title><![CDATA[job posting]]></title>
	<guid>http://www.nnseek.com/e/bionet.genome.arabidopsis/job_posting_101111538t.html</guid>
	<link>http://www.nnseek.com/e/bionet.genome.arabidopsis/job_posting_101111538t.html</link>
	<description><![CDATA[Please post this job to the list serve.  Thank you.  If you have any <br>questions, please let me know.<br><br>Lucy<br><br>*Postdoctoral Positions to Characterize Salicylic Acid Signaling Network <br>in Plants at Cornell Univ./BTI*<br><br> <br><br>The plant hormone salicylic acid (SA) affects many diverse processes in <br>plant growth and development and plays important role(s) in response to <br>abiotic and biotic stresses. Its role(s) in disease resistance has been <br>the most extensively studied but is still only partially understood <br>(e.g. PNAS 2005, 102:1773; Science 2007, 318:113; Curr. Opin. Plant <br>Biol. 2008, 11:436). To obtain insights into how SA carries out its <br>varied functions, a large number of putative SA-binding proteins <br>(pSABPs) have recently been identified in Arabidopsis by affinity <br>chromatography. Investigators will use two powerful high throughput <br>screens, an Arabidopsis protein micro-array and a yeast three hybrid <br>system, to identify additional SABPs, as well as confirm the SA-binding <br>activity of the already identified pSABPs. These SABPs will be <br>characterized using biochemical, genetic, molecular, bioinformatic, and <br>biophysical (X-ray crystallography) techniques to decipher their <br>functions in growth and development and/or responses to abiotic or <br>biotic stresses (particularly disease resistance), and the effects of SA <br>binding on these functions. Based on current data and the results <br>obtained, an SA signaling network model(s) will be constructed, tested <br>by more detailed characterization of putative signaling or regulatory <br>modules, and refined in order to produce an exemplary model of the SA <br>signaling network of SABPs which may serve as a paradigm for other plant <br>hormones (and other small ligands). This multi-disciplinary project will <br>be supported by a 4-year NSF 2010 grant. Applicant should have a Ph.D. <br>in biochemistry, molecular biology, chemistry, genetics, or related <br>areas and must be strongly motivated and dedicated to doing basic <br>research. */Strong background in protein chemistry and enzymology is <br>preferred./*<br>*/ /*<br><br>Send CV and a cover letter detailing experience and _have_ three letters <br>of recommendation sent to: Dan Klessig, Boyce Thompson Institute for <br>Plant Research at Cornell University, Tower Road, Ithaca, NY 14853 or <br>email dfk8@<a href="http://cornell.edu" rel="nofollow" class="url" target="_blank">cornell.edu</a> <br><mailto:dfk8@<a href="http://cornell.edu" rel="nofollow" class="url" target="_blank">cornell.edu</a>>.                                                                       <br>Related website <a href="http://bti.cornell.edu/DanKlessig.php" rel="nofollow" class="url" target="_blank">http://bti.cornell.edu/DanKlessig.php</a><br> <br><br>Institute Description: BTI is a not-for-profit research institute <br>affiliated with Cornell University. Its research emphasis is on <br>fundamentally understanding the basic biology of plants, particularly as <br>this relates to signal transduction within a plant and between a plant <br>and its environment. BTI is an Equal Opportunity/Affirmative Action <br>Employer.<br><br><br>-- <br>Lucy Pola, SPHR<br>Director of Human Resources<br>Boyce Thompson Institute<br>Tower Road<br>Ithaca, NY  14853<br><br>607-254-1239<br>lbp8@<a href="http://cornell.edu" rel="nofollow" class="url" target="_blank">cornell.edu</a><br><a href="http://bti.cornell.edu" rel="nofollow" class="url" target="_blank">http://bti.cornell.edu</a><br><br>
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        <td>Posted In: <a href="http://www.nnseek.com/e/bionet.genome.arabidopsis/">bionet.genome.arabidopsis</a></td>
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	<pubDate>Tue, 09 Sep 2008 12:27:00 PDT</pubDate>
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	<title><![CDATA[BAC Library construction]]></title>
	<guid>http://www.nnseek.com/e/bionet.genome.arabidopsis/bac_library_construction_101110770t.html</guid>
	<link>http://www.nnseek.com/e/bionet.genome.arabidopsis/bac_library_construction_101110770t.html</link>
	<description><![CDATA[Dear Sir,<br><br>I am a PhD student working in India . I have been attempting to construct a<br>High Molecular Weight (HMW) DNA library using<br>BAC but have been completely unsuccessful at producing clones. I know the<br>problem is with ligating the HMW DNA to the vector. I have already checked<br>the ligase and my vector and neither of those appears to be the problem. The<br>problem seems to be restricted to the HMW DNA.I am also worried about the<br>ligation reaction as I have already tried with different molar ratios as<br>advised in many papers but couldn't get any better result. Can you please<br>help me in this regard. Your help would be greatly appreciated.<br><br>Waiting for your kind reply,<br><br>Regards,<br><br>Sanjiban<br>
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	<pubDate>Tue, 09 Sep 2008 07:19:15 PDT</pubDate>
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