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        <title>Biowww.net RSS feed</title>
        <description><![CDATA[BioNews feeds from biowww dot net]]></description>
        <link>http://biowww.net/</link>
        <lastBuildDate>Fri, 04 Jul 2008 01:51:04 +0100</lastBuildDate>
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        <item>
            <title>Protein expression in E.Coli</title>
            <link>http://biowww.net/detail-250.html</link>
            <description>This protocol described a  strategy of parallel expression of a protein from a variety of vectors containing different tags and/or fusion partners, and a variety of E. coli host strains. 

The strategy to expression recombinant protein in e.coli involves two ...</description>
            <author>biowww</author>
        </item>
        <item>
            <title>Lambda protocol</title>
            <link>http://biowww.net/detail-273.html</link>
            <description>Protocol from Rob Phillips Group.
The well-known lambda bacteriophage grows on E. coli bacteria. Here's what you need to know to work with it. 

Preparation of plates with rich medium 
Preparation of liquid medium 
Titering lambda 
TM buffer for storage  ...</description>
            <author>biowww</author>
        </item>
        <item>
            <title>Bacterial cell culture</title>
            <link>http://biowww.net/detail-1414.html</link>
            <description>Bacterial cell culture general procedures:

Follow microbiology bacterial handling practice for all procedures.

- Streak agar plate from bacterial stock and grow overnight at 37c bacterial incubator.

- Transfer bacterial colony using sterile toothpick  ...</description>
            <author>biowww</author>
        </item>
        <item>
            <title>Generally useful protocols for phage and bacteria</title>
            <link>http://biowww.net/detail-272.html</link>
            <description>Here are some generally useful protocols for phage and bacteria. 

Preparation of plates with rich medium 
Preparation of liquid medium  ...</description>
            <author>biowww</author>
        </item>
        <item>
            <title>Bacteriology protocol</title>
            <link>http://biowww.net/detail-919.html</link>
            <description>PDF protocol for bacterial growing, storage and medium recipe etc. (From Marimoto lab at Northwestern University). ...</description>
            <author>biowww</author>
        </item>
        <item>
            <title>Prepare competent cells with RbCl2 method</title>
            <link>http://biowww.net/detail-920.html</link>
            <description>PDF protocol from Marimoto lab at Northwestern University. 

The procedure can be used to obtain competent cells with a transformation frequency of 10^6 - 10^7 colonies per microgram of DNA. Conveniently, these cells can be stored for months with relatively  ...</description>
            <author>biowww</author>
        </item>
        <item>
            <title>Preparation of E.Coli competent cells with CaCl2 method</title>
            <link>http://biowww.net/detail-921.html</link>
            <description>Preparation of E.Coli competent cells with CaCl2 method protocol from Marimoto lab at NothWestern University. (PDF file). ...</description>
            <author>biowww</author>
        </item>
        <item>
            <title>E. Coli Plasmid Vectors: Methods and Applications (Methods in Molecular Biology)</title>
            <link>http://biowww.net/detail-246.html</link>
            <description>E. Coli Plasmid Vectors: Methods and Applications (Methods in Molecular Biology (Clifton, ...</description>
            <author>biowww</author>
        </item>
        <item>
            <title>E.coli recombinant protein proteolysis</title>
            <link>http://biowww.net/detail-47.html</link>
            <description>We've been trying to express a pro-hormone as a GST fusion in E. coli 
 (DH5-alpha) but seem to be having problems with proteolysis - we think this 
 may be occuring at double basic sites but are not completely sure. 
 
 ... ...
 
 Click following links  ...</description>
            <author>biowww</author>
        </item>
        <item>
            <title>need help for the transformation</title>
            <link>http://biowww.net/detail-68.html</link>
            <description>I want to construct a DNA library with different sequence. First step, 
 PCR, the template contained random 40mers in the middle and normal 
 sequence on each end. After the PCR, I could obtain the PCR product 
 library and I ligated them into the plasmid v ...</description>
            <author>biowww</author>
        </item>
        <item>
            <title>Best vector for expressing recombinant antibody fragments?</title>
            <link>http://biowww.net/detail-91.html</link>
            <description>   Does anyone here express recombinant antibody fragments regularly in 
 their research? Which vector do you use and do you have to refold? I am 
 looking for one that gives me the highest yields (I know this depends on 
 individual sequences as well) and  ...</description>
            <author>biowww</author>
        </item>
        <item>
            <title>Protocol for making competent E coli</title>
            <link>http://biowww.net/detail-116.html</link>
            <description>Does anyone have a quick and simple way of making competent E coli for 
 transformation (heat shock)? ... ...
 
 ...</description>
            <author>biowww</author>
        </item>
        <item>
            <title>Plasmid or phagemid vector(s) holding large insert</title>
            <link>http://biowww.net/detail-137.html</link>
            <description>I am looking for plasmid or phagemid vector(s) which can hold 50kb DNA insert. I 
 appreciate it very much if anybody can send me information about the name of the plasmid and the place I can get it ... ...
 
 ...</description>
            <author>biowww</author>
        </item>
        <item>
            <title>Transformation efficiency</title>
            <link>http://biowww.net/detail-152.html</link>
            <description>If you are getting low transformation efficiency with chemically competent cells:
 
There were impurities in the DNA. Remove phenol, protein, detergents, and ethanol, by ethanol precipitation or GlassMAX DNA Isolation Systems. There was excess DNA. Use no mo ...</description>
            <author>biowww</author>
        </item>
        <item>
            <title>Glycerol stock longevity</title>
            <link>http://biowww.net/detail-215.html</link>
            <description>Does any one have information (data or opinion or personal experience) on 
 how 
 long a bacterial glycerol stock is viable @ -80oC? How often to stocks fail 
 to 
 regrow? Is is necessary to thaw and revitalize the stock at time intervals? 
 
  ...</description>
            <author>biowww</author>
        </item>
        <item>
            <title>E.Coli strain database (searchable)</title>
            <link>http://biowww.net/detail-251.html</link>
            <description>Large collection of E.Coli strains.

Large collection of E.Coli strains ...</description>
            <author>biowww</author>
        </item>
        <item>
            <title>PlasMapper Version 1.0 plasmid maps</title>
            <link>http://biowww.net/detail-796.html</link>
            <description>The PlasMapper server automatically generates and annotates plasmid maps using only the plasmid DNA sequence as input. Plasmid sequences up to 20,000 bp may be annotated and displayed. Plasmid figures may be rendered in PNG, JPG, SVG or SVGZ format. PlasMapper ...</description>
            <author>biowww</author>
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