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<title>Antibody Based Technologies</title>
<link>http://www.scientistsolutions.com/c202-antibody+based+technologies.html</link>
<description>Discussion on antibodies techniques  including polyclonal, monoclonal, peptide design, antisera, labeling, ELISA, fusion proteins, complement activation, isotypes, Fab, Fc, class switching…
 Life Science Discussion</description>
<language>en-us</language> 
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<sy:updateBase>2005-05-05T12:00+00:00</sy:updateBase>
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<title>Osteoblasts specific antibodies for Western blot</title>
<link>http://www.scientistsolutions.com/t26934-osteoblasts+specific+antibodies+for+western+blot.html</link>
<description><![CDATA[Hi,<br />Could any one suggest me some good working antibodies for osteoblasts specific markers such as Osteocalcin, BGLAP, Osteopontinand Dickkopf 1 ?? <br />Thanks in advance<br />]]></description>
<pubDate>Fri, 17 May 2013 05:39:27 GMT</pubDate>
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<title>atcc 5c8 supernatant storage ?</title>
<link>http://www.scientistsolutions.com/t26735-atcc+5c8+supernatant+storage+_.html</link>
<description><![CDATA[ hi <br />i'm asking if there is someone working with the atcc 5c8 CELL LINE (cat. num. HB-10916), in fact iwant to know if it's possible to storage the supernatant (used as anti CD154) and in under which conditions? <br />thank you ]]></description>
<pubDate>Wed, 01 May 2013 06:08:51 GMT</pubDate>
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<title>Phalloidin and Methanol</title>
<link>http://www.scientistsolutions.com/t26582-phalloidin+and+methanol.html</link>
<description><![CDATA[Hello everybody,<br />I'm facing a well known problem with phalloidin: it doesn't work with a fixation in Methanol.<br />My issue is that the only antibodies i have found for my protein of interest and working in immunocytochemistery are working with the fixation in Methanol.<br />Somebody told me that i should try to start with a PAF fixation, and then 5 minutes with Methanol.<br />What do you think about this? I'm working on mouse primary cortical neurons.<br />Thank you very much,<br />Rachel...]]></description>
<pubDate>Wed, 10 Apr 2013 02:38:20 GMT</pubDate>
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<title>antibodies for FACS and fluorescence microscopy</title>
<link>http://www.scientistsolutions.com/t26159-antibodies+for+facs+and+fluorescence+microscopy.html</link>
<description><![CDATA[i'am asking if we could use the same antibody for FACS analysis and fluorescence microscopy, if not what is the difference between the two kind of antibodies? <br />thanks  ]]></description>
<pubDate>Thu, 07 Mar 2013 01:54:29 GMT</pubDate>
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<title>inter-assay OD variation</title>
<link>http://www.scientistsolutions.com/t24882-inter_assay+od+variation.html</link>
<description><![CDATA[We are developing assays where we coat each time we do the assay, with  peptide,  overnight (2-8C in humidity box, same shelf of same  fridge each time, same 18hours each time).<br />Next day we block and add rabbit anti-peptide and then anti-rabbit HRP  and measure signal.  All steps are optimised and controls are good  (inter-precision 10% or less, intra precision 4%).<br />But the OD of the standard curve shifts a lot. - %CV of top standard OD  is 20%.  (Excluding extreme three ...]]></description>
<pubDate>Wed, 28 Nov 2012 06:29:20 GMT</pubDate>
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<title>WBCs</title>
<link>http://www.scientistsolutions.com/t24564-wbcs.html</link>
<description><![CDATA[ DID U KNOW THAT THERE ARE FIVE TYPES OF WHITE BLOOD CELLS?SURPRISINLY YES.....FIND OUT WHAT THEY ARE.<br />]]></description>
<pubDate>Tue, 23 Oct 2012 13:00:12 GMT</pubDate>
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<title>WBCs</title>
<link>http://www.scientistsolutions.com/t24563-wbcs.html</link>
<description><![CDATA[ DID U KNOW THAT THERE ARE FIVE TYPES OF WHITE BLOOD CELLS?SURPRISINLY YES.....FIND OUT WHAT THEY ARE.<br />]]></description>
<pubDate>Tue, 23 Oct 2012 12:57:44 GMT</pubDate>
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<title>HIV/Aids does have a cure</title>
<link>http://www.scientistsolutions.com/t24562-hiv_aids+does+have+a+cure.html</link>
<description><![CDATA[To every beginning is an end and the only solution is to look back and trace the creation of its roots,only then will it be understood.As a lab technician i see the solution but it will take just awhile until i can fully provide all verificationS.]]></description>
<pubDate>Mon, 22 Oct 2012 11:09:58 GMT</pubDate>
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<title>western blotting</title>
<link>http://www.scientistsolutions.com/t24560-western+blotting.html</link>
<description><![CDATA[<br />In western blotting first we do sds page na that time all the proteins will be linearised..<br />But after that wen we MAbs (which can recognise conformational and linear epitopes)to identify  binds to the linearised protein how? that time as such there is no <br />conformational epitope na then how it binds...<br />wat is the mechanism behind it....<br />Thank you...]]></description>
<pubDate>Sat, 20 Oct 2012 05:59:25 GMT</pubDate>
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<title>Where do you buy antibodies?</title>
<link>http://www.scientistsolutions.com/t24501-where+do+you+buy+antibodies_.html</link>
<description><![CDATA[I work for a company that develops and sales quality antibodies. As these antibodies perfom as expected by the scientists who use them, I would like more scientists to benefit from them in their research. For that I need to learn where the scientists buy their antibodies.<br />Can you tell me on which website you go when looking for a primary antibody? a secondary antibody?<br />Thank you very much!<br />]]></description>
<pubDate>Thu, 11 Oct 2012 07:17:04 GMT</pubDate>
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<title>Antibodies</title>
<link>http://www.scientistsolutions.com/t24117-antibodies.html</link>
<description><![CDATA[Hello,<br />I have only idea that Antibodies are produced by a type of white blood cell called a plasma cell. Antibodies can occur in two physical forms, a soluble form that is secreted from the cell, and a membrane-bound form that is attached to the surface of a B cell and is referred to as the B cell receptor (BCR). Some antibodies act by binding to certain essential enzymes in the target bacteria. So, I want to know that how might these antibiotics influence the chemical reactions controlle...]]></description>
<pubDate>Thu, 13 Sep 2012 21:33:13 GMT</pubDate>
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<title>How long do mold antibodies stay in your blood stream?</title>
<link>http://www.scientistsolutions.com/t24097-how+long+do+mold+antibodies+stay+in+your+blood+stream_.html</link>
<description><![CDATA[Hi all,<br />My sister was getting allergy tested next Tuesday because of severe  reaction to some kind of mold in her apartment. I read somewhere that  mold antibodies produced from an allergy stay in your stream for around  30 days, but that was the only information I could really find. So, now I  am in doubt. Any one having knowledge please suggest me.<br />Thanks!  <br />Stephen Jones ]]></description>
<pubDate>Thu, 06 Sep 2012 21:51:35 GMT</pubDate>
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<title>PrP antibodies specific to PrPc or PrPsc</title>
<link>http://www.scientistsolutions.com/t23625-prp+antibodies+specific+to+prpc+or+prpsc.html</link>
<description><![CDATA[ Hi!<br />I have been looking the past few days for antibodies to recognize the native PrPc and PrPsc of mouse. <br />So far, I think I have found some good candidates, but I am wondering if anyone here is a prion specialist and might be able to help me out with options.<br />I need an Ab that will recognize both PrPc and PrPsc in their native states - without denaturing or Proteinase <br />K.<br />Also, an Ab that will recognize ONY PrPc in int native state.<br />An...]]></description>
<pubDate>Mon, 23 Jul 2012 13:12:14 GMT</pubDate>
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<title>Protein expression.</title>
<link>http://www.scientistsolutions.com/t23445-protein+expression_.html</link>
<description><![CDATA[<br />Dear All,<br />I'm trying to get the soluble expression of Fab(Fragment of Antibody) in cytoplasma of E.coli.I have gone through the no of litratures and tried some experiment but not getting enough expression.<br />Actually my question is that ,What we can do as a upstream member (fermentation) to get the good level of soluble expression in e.coli?<br />I have tried lower temprature,lower agitation,low level of inducer concentration and used some modified media also to get the solu...]]></description>
<pubDate>Thu, 05 Jul 2012 09:46:10 GMT</pubDate>
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<title>Affinity Purification of Chicken Antibodies</title>
<link>http://www.scientistsolutions.com/t23407-affinity+purification+of+chicken+antibodies.html</link>
<description><![CDATA[ We are attemptting to do a affinity purification of some IgY. We made a column using the protein. Blocked it. And then added our antibody. We have tried several elutions with no success. Does anyone know the secret? Any assistance would be appreciated.]]></description>
<pubDate>Thu, 21 Jun 2012 10:11:56 GMT</pubDate>
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<title>DAB destain, is this possible?</title>
<link>http://www.scientistsolutions.com/t22738-dab+destain%2c+is+this+possible_.html</link>
<description><![CDATA[We have completed an immunohistochemical stain having used DAB as the chromagen.  We now would like to use this same tissue section for another antibody.  Is it possible to remove the DAB staining somehow?]]></description>
<pubDate>Fri, 06 Apr 2012 09:27:46 GMT</pubDate>
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<title>How to separate A/G beads from the attached antibodies?</title>
<link>http://www.scientistsolutions.com/t21055-how+to+separate+a_g+beads+from+the+attached+antibodies_.html</link>
<description><![CDATA[I want to pull down my vesicle of interest with antibody coated A/G beads, but, the problem is I want to separate the vesicle from the beads and use that vesicle for other purpose. Does anyone know if there is way to get stuff off the beads without heating? Also, I want to avoid using magnetic beads.<br />Thanks<br />VS<br />]]></description>
<pubDate>Fri, 04 Nov 2011 12:16:57 GMT</pubDate>
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<title>ELISA Validation</title>
<link>http://www.scientistsolutions.com/t20601-elisa+validation.html</link>
<description><![CDATA[Hii all,<br />Does anyone have a protocol for immunoassays validation as I can't find clear guidelines for this??<br />or at least if anybody can provide me with any guidelines for the validation of immunoassays.<br />thank you]]></description>
<pubDate>Wed, 28 Sep 2011 05:20:53 GMT</pubDate>
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<title>ELISA, What is the Best Fit for the Standard Curve?</title>
<link>http://www.scientistsolutions.com/t20485-elisa%2c+what+is+the+best+fit+for+the+standard+curve_.html</link>
<description><![CDATA[<br />Help!  :(<br />I'm working on ELISA, using ELISA kit ready coated, ELISA reader with software.<br />I make dilution series to create standard curve (1000 pg/ml, 500, 250, 125, 62, 31, 15) but sometimes I apply in the reaction only 5 std.<br />the cytokine i'm working with has very low level in human serum, almost around the lowest std. (15 pg/ml)<br />I got std. curve with R^2 &amp;gt; 0.99 which is very good but still not enough, because I need almost perfect std. curv...]]></description>
<pubDate>Mon, 19 Sep 2011 05:44:10 GMT</pubDate>
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<title>Are IgGs secreted in the gut?</title>
<link>http://www.scientistsolutions.com/t20098-are+iggs+secreted+in+the+gut_.html</link>
<description><![CDATA[Hi,<br />  I was reading a paper about a phase II clinical trial involving IV injection of monoclonal anti-toxin IgGs againt C. difficile toxine A and B. I thought that only IgA were secreted in the gut... How can an IV of IgG be effective against a bug in the gut? <br />(Leav et al 2010 Vaccine 28 (2010) 965&amp;ndash;969)<br />Thanks<br />]]></description>
<pubDate>Mon, 22 Aug 2011 17:14:45 GMT</pubDate>
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