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Sökning: L773:1940 6029 > (2020)

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1.
  • Altai, Mohamed, et al. (författare)
  • Preparation of Conjugates for Affibody-Based PNA-Mediated Pretargeting.
  • 2020
  • Ingår i: Methods in Molecular Biology. - New York, NY : Springer US. - 1064-3745 .- 1940-6029. ; 2105, s. 283-304, s. 283-304
  • Tidskriftsartikel (refereegranskat)abstract
    • Affibody molecules are small engineered scaffold proteins suitable for in vivo tumor targeting. Radionuclide molecular imaging using directly radiolabelled affibody molecules provides excellent imaging. However, affibody molecules have a high renal reabsorption, which complicates their use for radionuclide therapy. The high renal reabsorption is a common problem for the use of engineered scaffold proteins for radionuclide therapy. Affibody-based PNA-mediated pretargeting reduces dramatically the absorbed dose to the kidneys and makes affibody-based radionuclide therapy possible. This methodology might, hopefully, solve the problem of high renal reabsorption for radionuclide therapy mediated by other engineered scaffold proteins.
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  • Barreby, E, et al. (författare)
  • Kupffer Cell mRNA Sequencing
  • 2020
  • Ingår i: Methods in molecular biology (Clifton, N.J.). - New York, NY : Springer US. - 1940-6029. ; 2164, s. 27-44
  • Tidskriftsartikel (refereegranskat)
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4.
  • Christoffersson, G, et al. (författare)
  • Mouse Models of Virus-Induced Type 1 Diabetes
  • 2020
  • Ingår i: Methods in molecular biology (Clifton, N.J.). - New York, NY : Springer US. - 1940-6029. ; 2128, s. 93-105
  • Tidskriftsartikel (refereegranskat)
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5.
  • Dahlgren, Claes, 1949, et al. (författare)
  • Measurement of Respiratory Burst Products, Released or Retained, During Activation of Professional Phagocytes.
  • 2020
  • Ingår i: Methods in molecular biology (Clifton, N.J.) Vol 2087.. - New York, NY : Springer. - 1940-6029. - 9781071601532 ; , s. 301-324
  • Bokkapitel (refereegranskat)abstract
    • Activation of professional phagocytes, potent microbial killers of our innate immune system, is associated with an increased cellular consumption of molecular oxygen (O2). The O2 molecules consumed are reduced by electrons delivered by a membrane localized NADPH-oxidase that initially generate one- and two electron reduced superoxide anions (O2-) and hydrogen peroxide (H2O2), respectively. These oxidants can then be processed into other highly reactive oxygen species (ROS) that can kill microbes, but that may also cause tissue destruction and drive other immune cells into apoptosis. The development of basic techniques to measure and quantify ROS generation by phagocytes is of great importance, and a large number of methods have been used for this purpose. A selection of methods (including chemiluminescence amplified by luminol or isoluminol, absorbance change following reduction of cytochrome c, and fluorescence increase upon oxidation of PHPA) are described in detail in this chapter with special emphasis on how to distinguish between ROS that are released extracellularly, and those that are retained within intracellular organelles. These techniques can be valuable tools in research spanning from basic phagocyte biology to diagnosis of diseases linked to the NADPH-oxidase and more clinically oriented research on innate immune mechanisms and inflammation.
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  • Isaksson, Linnéa, et al. (författare)
  • Cell-Free Protein Synthesis of Small Intrinsically Disordered Proteins for NMR Spectroscopy
  • 2020
  • Ingår i: Methods in molecular biology (Clifton, N.J.). - New York, NY : Springer US. - 1940-6029. ; 2141, s. 233-245
  • Tidskriftsartikel (refereegranskat)abstract
    • Cell-free protein synthesis (CFPS) is an established method to produce recombinant proteins and has been used in a wide variety of applications. The use of CFPS has almost from the onset been favorably linked to the production of isotopically labelled proteins for NMR spectroscopy as the resulting labelling of the produced protein is defined by the chosen amino acids during reaction setup. Here we describe how to set up production and isotopic labelling of small intrinsically disordered proteins (IDPs) for NMR spectroscopy applications using an E. coli-based CFPS system in batch mode.
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9.
  • Jensen, Kristine Steen (författare)
  • Measuring and Analyzing Binding Kinetics of Coupled Folding and Binding Reactions Under Pseudo-First-Order Conditions
  • 2020
  • Ingår i: Methods in molecular biology (Clifton, N.J.). - New York, NY : Springer US. - 1940-6029. ; 2141, s. 629-650
  • Tidskriftsartikel (refereegranskat)abstract
    • Many intrinsically disordered proteins (IDPs) adopt a well-defined structure upon binding to their interaction partners. Kinetic characterization is a requirement for the investigation of the dynamics and mechanisms of these folding-upon-binding reactions. Here a protocol is described for the investigation of binding kinetics of bimolecular binding and folding reactions of IDPs to their ligand partner under pseudo-first-order conditions using stopped-flow mixing and fluorescence detection.
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