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Sökning: L773:1940 6029

  • Resultat 341-350 av 503
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341.
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342.
  • Pasetto, A, et al. (författare)
  • T-Cell Repertoire Characterization
  • 2022
  • Ingår i: Methods in molecular biology (Clifton, N.J.). - New York, NY : Springer US. - 1940-6029. ; 2574, s. 209-219
  • Tidskriftsartikel (refereegranskat)
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343.
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344.
  • Pejler, Gunnar, et al. (författare)
  • Serglycin- the master of the mast cell
  • 2012
  • Ingår i: Methods in Molecular Biology. - Totowa, NJ : Humana Press. - 1064-3745 .- 1940-6029. ; 836, s. 201-217
  • Tidskriftsartikel (refereegranskat)
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345.
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346.
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347.
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348.
  • Persson, Andrea, et al. (författare)
  • Production and HPLC-Based Disaccharide Analysis of Xyloside-Primed Glycosaminoglycans
  • 2022
  • Ingår i: Glycosaminoglycans. Methods in Molecular Biology, vol 2303. Balagurunathan K., Nakato H., Desai U., Saijoh Y. (eds). - New York, NY : Springer. - 1064-3745 .- 1940-6029. - 9781071613986 ; , s. 173-182
  • Bokkapitel (övrigt vetenskapligt/konstnärligt)abstract
    • Although glycosaminoglycans (GAGs) are known to be involved in a variety of physiological and pathological processes, knowledge about their expression by cells or tissues, the GAGome, is limited. Xylosides can be used to induce the formation of GAGs without the presence of a proteoglycan core protein. The administration of xylosides to living cells tends to result in a considerable amplification in GAG production, and the xylosides can, therefore, be used as analytical tools to study the GAG produced by a certain cell type. One of the most common ways to analyze the GAGs structurally is by disaccharide analysis, which involves depolymerization of the GAGs into disaccharides, fluorescent labeling of the disaccharides with 2-aminoacridone, and quantification using high-pressure liquid chromatography (HPLC). Here, we describe the procedure of producing xyloside-primed GAGs and how to study them structurally by disaccharide analysis. © 2022, Springer Science+Business Media, LLC, part of Springer Nature.
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349.
  • Persson, Helena, et al. (författare)
  • Antibody validation by immunoprecipitation followed by mass spectrometry analysis
  • 2017
  • Ingår i: Methods in Molecular Biology. - New York, NY : Humana Press Inc.. ; 1575, s. 175-187
  • Konferensbidrag (refereegranskat)abstract
    • We describe a mass spectrometry-based approach for validation of antibody specificity. This method allows validation of antibodies or antibody fragments, against their endogenous targets. It can assess if the antibody is able to bind to its native antigen in cell lysates among thousands of other proteins, DNA, RNA, and other cellular components. In addition, it identifies other proteins the antibody is able to immunoprecipitate allowing for the assessment of antibody specificity and selectivity. This method is easily scalable, adaptable to different cell lines and conditions and has been shown to be reproducible between multiple laboratories.
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350.
  • Pettersson, Mats, et al. (författare)
  • Capacitating epistasis--detection and role in the genetic architecture of complex traits.
  • 2015
  • Ingår i: Methods in Molecular Biology. - New York, NY : Springer New York. - 1064-3745 .- 1940-6029. ; 1253:1253, s. 185-196
  • Tidskriftsartikel (refereegranskat)abstract
    • Here, we discuss the potential role of capacitating epistasis in the genetic architecture of complex traits. Two alternative methods for identifying such gene-gene interactions in genetic association studies-mapping of variance controlling loci and the variance plane ratio (VPR) method-are introduced. An overview of the theoretical foundation of the methods is presented together with a discussion on their implementation and available software for performing these analyses. We conclude by highlighting a few examples of capacitating epistasis described in the literature and its potential impacts on the genetics of complex traits.
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  • Resultat 341-350 av 503
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