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Artykuły w czasopismach na temat "Chemical affinity"
Košíková, Božena, Elena Sláviková i Juraj Lábaj. "Affinity of lignin preparations towards genotoxic compounds". BioResources 4, nr 1 (17.11.2008): 72–79. http://dx.doi.org/10.15376/biores.4.1.72-79.
Pełny tekst źródłaKauvar, Lawrence M., Hugo O. Villar, J. Richard Sportsman, Deborah L. Higgins i Donald E. Schmidt. "Protein affinity map of chemical space". Journal of Chromatography B: Biomedical Sciences and Applications 715, nr 1 (wrzesień 1998): 93–102. http://dx.doi.org/10.1016/s0378-4347(98)00045-0.
Pełny tekst źródłaPARIKH, INDU, i PEDRO CUATRECASAS. "AFFINITY CHROMATOGRAPHY". Chemical & Engineering News 63, nr 34 (26.08.1985): 17–32. http://dx.doi.org/10.1021/cen-v063n034.p017.
Pełny tekst źródłaOhno, K., Y. Inoue i M. Sakurai. "Quantum Chemical Study of Antibody Affinity Maturation". Seibutsu Butsuri 43, supplement (2003): S50. http://dx.doi.org/10.2142/biophys.43.s50_4.
Pełny tekst źródłaAlcantara, R. E., C. Xu, T. G. Spiro i V. Guallar. "A quantum-chemical picture of hemoglobin affinity". Proceedings of the National Academy of Sciences 104, nr 47 (14.11.2007): 18451–55. http://dx.doi.org/10.1073/pnas.0706026104.
Pełny tekst źródłaHornung, M. W., M. A. Tapper, J. S. Denny, R. C. Kolanczyk, B. R. Sheedy, P. C. Hartig, H. Aladjov, T. R. Henry i P. K. Schmieder. "Effects-based chemical category approach for prioritization of low affinity estrogenic chemicals". SAR and QSAR in Environmental Research 25, nr 4 (3.04.2014): 289–323. http://dx.doi.org/10.1080/1062936x.2014.898692.
Pełny tekst źródłaSchmieder, P., Ovanes Mekenyan, Steven Bradbury i G. Veith. "QSAR prioritization of chemical inventories for endocrine disruptor testing". Pure and Applied Chemistry 75, nr 11-12 (1.01.2003): 2389–96. http://dx.doi.org/10.1351/pac200375112389.
Pełny tekst źródłaFreidin, A. B. "On the chemical affinity tensor for chemical reactions in deformable materials". Mechanics of Solids 50, nr 3 (maj 2015): 260–85. http://dx.doi.org/10.3103/s0025654415030048.
Pełny tekst źródłaNayarisseri, Anuraj. "Experimental and Computational Approaches to Improve Binding Affinity in Chemical Biology and Drug Discovery". Current Topics in Medicinal Chemistry 20, nr 19 (14.09.2020): 1651–60. http://dx.doi.org/10.2174/156802662019200701164759.
Pełny tekst źródłaNowak, Damian, Rafał Adam Bachorz i Marcin Hoffmann. "Neural Networks in the Design of Molecules with Affinity to Selected Protein Domains". International Journal of Molecular Sciences 24, nr 2 (16.01.2023): 1762. http://dx.doi.org/10.3390/ijms24021762.
Pełny tekst źródłaRozprawy doktorskie na temat "Chemical affinity"
Lindgren, Joel. "Chemical Engineering of Small Affinity Proteins". Doctoral thesis, KTH, Proteinteknologi, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-141014.
Pełny tekst źródłaQC 20140207
Zourna, Kalliopi. "Smart magnetic affinity adsorbents". Thesis, University of Birmingham, 2009. http://etheses.bham.ac.uk//id/eprint/511/.
Pełny tekst źródłaBeard, Hester Annie. "Affinity-guided chemical probes for the study of protein interactions". Thesis, University of Leeds, 2018. http://etheses.whiterose.ac.uk/20637/.
Pełny tekst źródłaTarasova, Anna Optometry UNSW. "Fabrication and characterisation of affinity-bound liposomes". Awarded by:University of New South Wales. Optometry, 2007. http://handle.unsw.edu.au/1959.4/29114.
Pełny tekst źródłaZulqarnain, Kamran. "Scale-up of affinity separation based on magnetic support particles". Thesis, University College London (University of London), 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.313426.
Pełny tekst źródłaStewart, David Johnston. "Immobilisation of triazine dyes on inert hydrophobic supports for affinity chromatography". Thesis, University of Cambridge, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.315974.
Pełny tekst źródłaMiller, Eric Alexander. "Development of thermostable affinity reagents for low-cost, paper-based medical diagnostics". Thesis, Massachusetts Institute of Technology, 2019. https://hdl.handle.net/1721.1/122849.
Pełny tekst źródłaCataloged from PDF version of thesis.
Includes bibliographical references.
The timely diagnosis and treatment of disease in resource-constrained settings requires the development of robust point-of-care (POC) diagnostics, which provide accurate results and can be employed by users with minimal medical training and limited access to basic infrastructure. One of the most common POC diagnostic formats is the immunochromatographic rapid diagnostic test, which traditionally uses nitrocellulose-immobilized IgG antibodies as binding proteins for the capture of disease biomarkers from patient samples. However, these antibodies are expensive to produce and structurally complex, and are prone to thermal denaturation. In contexts where continuous cold chain storage may be infeasible, the resulting loss in binding activity can manifest as diminished assay sensitivity, leading to adverse clinical outcomes and eroding patient trust in the diagnostic format.
In the interest of replacing diagnostic antibodies with a more cost-effective, robust class of binding proteins, this thesis explores the development of thermostable affinity reagents based on the hyperthermophilic scaffold protein rcSso7d. Given its native microbial host, minimalist structure, and high wild-type melting temperature (98°C), rcSso7d represents a viable alternative to antibodies in in vitro POC assays. To assess the applicability of the rcSso7d scaffold in this context, protein engineering techniques were used to rapidly select analyte-specific binding variants from a yeast surface display library of >109 members. A high-affinity rcSso7d binder was identified, produced in high yield in a bacterial host, and readily purified in a single chromatographic step.
The in vitro activity and thermal stability of this engineered binder were characterized in the context of a low-cost, paper-based assay, and significant improvements in stability and production economics were observed for rcSso7d-based assays, relative to assays featuring a representative antibody reagent. Additionally, general strategies were developed to improve the diagnostic performance of paper-based assays employing rcSso7d-based reagents. In one instance, chimeric protein constructs in which rcSso7d variants are fused to a cellulose-binding domain were found to bind to unmodified cellulose in an oriented fashion and with high efficiency. This substrate anchoring approach permits the rapid, high-density immobilization of the rcSso7d species in paper-based assays, and yields significant sensitivity enhancement by enabling both the depletion of the soluble analyte from the sample, and the processing of large sample volumes within clinically relevant timescales.
Detection reagents incorporating rcSso7d binders were also developed, using novel fusion constructs which enabled in vivo labelling while preserving analyte binding activity. These techniques were applied in the context of a urine-based tuberculosis biomarker, and may one day permit the development of multiplexed assays targeting a suite of these analytes. Such a development would enable point-of-care diagnostic testing without requiring the production of sputa, facilitating disease detection in otherwise inaccessible patient populations (e.g. children under five, the elderly, and immunocompromised patients).
"People who have financially supported this thesis: the NIH Biotechnology Training Program, the Tata Center for Technology and Design, the Deshpande Center, the Sandbox program, and the Singapore- MIT Alliance for Research and Technology"
by Eric Alexander Miller.
Ph. D.
Ph.D. Massachusetts Institute of Technology, Department of Chemical Engineering
Hsu, Kuang-Hsin. "Scale-up of affinity chromatography for protein purifications". Ohio : Ohio University, 2000. http://www.ohiolink.edu/etd/view.cgi?ohiou1172002240.
Pełny tekst źródłaLam, Hei Ning Henry. "Electrostatic and affinity enhancements of protein partitioning in two-phase aqueous micellar systems". Thesis, Massachusetts Institute of Technology, 2005. http://hdl.handle.net/1721.1/33700.
Pełny tekst źródłaIncludes bibliographical references (p. 175-188).
This thesis was motivated by the practical need to develop a scalable and cost-effective separation method for low-cost, high-volume protein products. This unmet challenge can potentially be addressed by extraction in two-phase aqueous micellar systems, in which biomolecules can be partitioned in mild, predominantly aqueous environments. The goal of this thesis was to explore various ways of enhancing protein partitioning in two-phase aqueous micellar systems, by the incorporation of electrostatic and affinity interactions, to obtain satisfactory yield and specificity for the purification of industrially relevant hydrophilic proteins. The electrostatically-enhanced partitioning of the enzyme glucose-6-phosphate dehydrogenase (G6PD) in two-phase aqueous mixed (nonionic/cationic) micellar systems was investigated experimentally and theoretically. The successful enhancement, up to 22-fold, of the partitioning of the negatively-charged G6PD was attained by adding the positively- charged surfactant alkyltrimethylammonium bromide (CnTAB) to form charged mixed micelles with the phase-forming nonionic surfactant, decyl tetra(ethylene oxide) (C₁₀E₄).
(cont.) The effects of the tail length of the positively-charged surfactant on protein denaturation and protein partitioning behavior were also studied. Furthermore, the experimental results were used to validate a predictive theory for electrostatic enhancement. In the area of affinity enhancement, the affinity-enhanced partitioning of an engineered affinity-tagged protein, CBM9-GFP (Green Fluorescent Protein linked to a carbohydrate- binding module), in two-phase aqueous micellar systems was investigated experimentally and theoretically. The experimental results showed that the partition coefficient of the target protein, CBM9-GFP, can be improved more than 6-fold, by virtue of the affinity interactions, and that the enhancement is specific to the target protein. The system utilized requires only one surfactant, decyl [beta]-D-glucopyranoside (C₁₀G₁), which acts simultaneously as the affinity ligand and as the phase-forming surfactant, and as such, has important practical advantages. A novel theoretical framework to describe affinity- enhanced protein partitioning in two-phase aqueous micellar systems was developed and validated experimentally. In addition, the separation method developed was successfully applied to a real cell lysate.
(cont.) It was found that the protein impurities in the cell lysate do not interfere with the partitioning of the target protein (CBM9-GFP) at industrially relevant concentrations, and that the protein impurities were concentrated away from the target protein. Lastly, the theoretical description developed was used to identify various strategies for improving the affinity-enhanced partitioning of the target protein in two-phase aqueous micellar systems. Although more work remains to be done before the separation methods studied in this thesis can reach their full potential and be eventually commercialized, this thesis nevertheless represents an essential starting point for future efforts to improve, extend, and commercialize this promising bioseparation method.
by Hei Ning Henry Lam.
Ph.D.
Liebenberg, Liesl Eileen. "Non-covalent immobilisation of a ligand system : a new approach to affinity separation". Thesis, Stellenbosch : Stellenbosch University, 2003. http://hdl.handle.net/10019.1/53522.
Pełny tekst źródłaENGLISH ABSTRACT: Advances in pharmacology, biochemistry and biotechnology are increasingly dependant upon affinity chromatography as a preferred separation technique for the purification and characterisation of specific biomolecules. In the past few years avidin-biotin technology has been widely and successfully used in the fields of medicine, pharmacy, biology and biochemistry. The avidin-biotin complex (ABC) has been used as a mediator for affinity chromatography, affinity cytochemistry, immunoassay, histopathology, bioaffinity sensors, erosslinking and immobilisation studies. The main reason for the popularity of the ABC and its growing usefulness in biotechnology is the exceptionally high affinity (1015 M-l) and stability of the noncovalent interaction between avidin and biotin. The use of the ABC is broadening as different biotin derivatives and avidin-containing conjugates are becoming commercially available. The aim of this work was to evaluate the usefulness of a plutonic" FI 08 and the ABC conjugate to effect affinity separation. Towards this aim, the adsorption of plutonic" F108 onto hydrophobic polysulphone membrane surfaces was studied. This information was used to determine the theoretical maximum amount of pluronic" FI08 that will adsorb onto a unit surface area of the membrane. It is known that the polypropylene oxide (PPO) centre block ofthe pluronic" F I08 surfactant molecule governs the concentration of pluronic" F I 08 molecules that will adsorb onto a given hydrophobic surface. If the maximum coating concentration of plutonic" FI08 is known, one can assume that the maximum coating concentration of any pluronic derivative, with the same PPO centre block size, will be the same. Adsorption studies were carried out, the Langmuir adsorption isotherm was determined, and subsequently the fractional coating was calculated. The end-groups of plutonic" FI08 were modified as follows and the substituted pluronic was adsorbed onto a membrane that was to act as the solid support matrix in the development of an affinity system: Amino pluronic was synthesised by first tosylating pluronic" FI08, followed by azidation with NaN3 then reduction with LiAI~. The synthesised amino pluronic was then biotinylated using N-hydroxysuccinimide biotin ester. The suitability of this synthetic route was first assessed on a model compound, 2-methoxyethylamine, and validated by NMR (Nuclear Magnetic Resonance) spectroscopy. The synthetic protocol was then used to derivatise the larger pluronic molecule. The affinity system was tested on two different hydrophobic surfaces: polystyrene and polysulphone membranes (PSMs). Avidin-conjugated horseradish peroxidase was obtained and used to interact with the immobilised biotin. The enzymatic reaction of the coupled peroxidase converted the substrate, 2, 2'-azino-di-(3-ethyl-benzthiazoline-6-sulphonic acid) (ABTS) to a coloured product. The colour developed is proportional to the amount of biotin that was immobilised on the hydrophobic surfaces studied. Non-covalent immobilisation of the synthesised biotin-pluronic molecule was successfully obtained onto the hydrophobic polystyrene as well as the polysulphone membrane surfaces.
AFRIKAANSE OPSOMMING: Vooruitgang in die farmakologie, biochemie en biotegnologie word al meer afhanklik van affiniteits chromatografie as die verkose tegniek vir die suiwering en karaterisering van spesifieke biomolekules. Oor die afgelope jare het die avidien-biotien tegnologie homself as baie bruikbaar bewys in die mediese, farmakologiese, biologiese en biochemiese velde. Toepassings waar die avidien-biotien kompleks betrokke was sluit in die toepassing as 'n mediator vir affiniteits chromatografie, affiniteits sitologie, immuno bepalings, histopatologie, bioaffiniteits sensors sowel as kruisbinding en immobiliserings studies en vele meer. Die hoofrede vir die gewildheid van die avidien-biotien kompleks en die groeiende bruikbaarheid in die biotegnologie is die buitengewone hoë affiniteit (l015 M-I ) en stabiliteit van die nie-kovalente interaksie tussen avidien en biotien. Die toepassingsveld van die avidien-biotien kompleks word wyer met die verskeidenheid biotien derivate en avidien-bevattende konjugate wat kommersiëel beskikbaar is. Die doel van die werk wat hier gedokumenteer word is om die bruikbaarheid van Plutonic" FI08 en die avidien-biotien kompleks, vir gebruik in 'n affiniteits chromatografie sisteem, te evalueer. Om hierdie doel te bereik is die adsorpsie van Pluronic" FI08 aan hidrofobiese polisulfoon membraan oppervlaktes bestudeer. Die eksperimentele data wat gegenireer is, is gebruik om die teoretiese maksimum hoeveelheid Pluronic wat per eenheids oppervlakte membraan adsorbeer te bepaal. Dit is reeds bekend dat die polipropileen (PPO) middel blok van die Pluronic emulgant die konsentrasie van die geadsorbeerde Pluronic molekules op 'n gegewe hidrofobiese oppervlakte bepaal. Indien die maksimum bedekkingskonsentrasie VIr maksimum oppervlakbedekking van Plutonic" FI08 bekend is, kan teoreties aanvaar word dat die bedekkingskonsentrasie vir enige Pluronic derivaat met dieselfde grootte PPO blok dieselfde sal wees. Adsorpsiestudies was uitgevoer om die Langmuir adsorpsie isoterm te bepaal. Daaropvolgend was die fraksionele bedekking bereken. Amino-pluronic was gesintetiseer deur die eindpunte van Pluronic te derivatiseer. Hierdie Pluronic derivaat was gevolglik geadsorbeer aan 'n membraan wat gedien het as die soliede oppervlakte vir die ontwikkeling van 'n affiniteits chromatografie sisteem. Amino-pluronic was gesintetiseer deur Pluronic eers te tosileer en daarna te asideer met NaN3 en laastens te reduseer met LiAI~. Die produk was gebiotinileer deur gebruik te maak van N-hidroksisuksinimied-biotien-ester. Die bruikbaarheid van hierdie sintetiese roete is eers bepaal deur van 'n model verbinding, 2-metoksiëtielamien, gebruik te maak en dit met behulp van KMR (Kern Magnetiese Resonans) spektroskopie te karakteriseer. Die affiniteits sisteem is getoets op twee verskillende hidrofobiese oppervlaktes naamlik polistireen en polisulfoon membraan oppervlaktes. Avidien gekonjugeerd met 'n peroksiedase ensiem is gebruik om met die geïmmobiliseerde biotien te assosieer. Die ensiematiese reaksie van die gekoppelde peroksiedase het die substraat 2, 2' -azino-di-(3-etiel-benzthiazolien-6-sulfoonsuur) (ABTS) omgesit na 'n gekleurde produk, waar dit teenwoordig is. 'n Reeks wasstappe is gebruik om die gemodifiseerde peroksidase ensiem wat nie aan die hidrofobiese oppervlakte gekoppel nie, weg te spoel. Hierdeur is die mate van binding aan die hirofobiese oppervlakte gekwantifiseer deur die kleur te kwantifiseer wat ontwikkelomdat die kleurontwikkeling direk proporsioneel is aan die hoeveelheid peroksidase wat nog aan die membraan gekoppel is. Nie-kovalente immobilisasie van die gesintetiseerde biotien-pluronic molekule is suksesvolop beide die hidrofobiese polistireen oppervlakte sowel as die polisulfoon membraan verkry.
Książki na temat "Chemical affinity"
Wrotnowski, Cort. Affinity technology. Norwalk, CT: Business Communications Co., 1991.
Znajdź pełny tekst źródłaSadoun-Goupil, Michelle. Du flou au clair? Histoire de l'affinité chimique: De Cardan à Prigogine. Paris: Ed. du C.T.H.S., 1991.
Znajdź pełny tekst źródłaSadoun-Goupil, Michelle. Du flou au clair?: Histoire de l'affinité chimique de Cardan à Prigogine. Paris: Éditions du C.T.H.S., 1991.
Znajdź pełny tekst źródłaAndrew, Kenney, i Fowell Susan, red. Practical protein chromatography. Totowa, N.J: Humana Press, 1992.
Znajdź pełny tekst źródłaTsukahara, Togo. Affinity and shinwa ryoku: Introduction of western chemical concepts in early nineteenth-century Japan. Amsterdam: J.C. Gieben, 1993.
Znajdź pełny tekst źródłaA, Olah George. Superelectrophiles and their chemistry. Hoboken, N.J: John Wiley, 2007.
Znajdź pełny tekst źródła1964-, Yang Xueming, i Liu Kopin, red. Modern trends in chemical reaction dynamics. Singapore: World Scientific, 2004.
Znajdź pełny tekst źródłaL, Krainsky I., i United States. National Aeronautics and Space Administration., red. Negative electron affinity effect on the surface of chemical vapor deposited diamond polycrystalline films. [Washington, D.C: National Aeronautics and Space Administration, 1996.
Znajdź pełny tekst źródłaW, Ball David, i Lewis Research Center, red. Theoretical and experimental determination of the proton affinity of (CF₃CH₂)₂O. [Cleveland, Ohio]: National Aeronautics and Space Administration, Lewis Research Center, 1998.
Znajdź pełny tekst źródłaW, Ball David, i Lewis Research Center, red. Theoretical and experimental determination of the proton affinity of (CF₃CH₂)₂O. [Cleveland, Ohio]: National Aeronautics and Space Administration, Lewis Research Center, 1998.
Znajdź pełny tekst źródłaCzęści książek na temat "Chemical affinity"
Carredano, Enrique, i Herbert Baumann. "Affinity Ligands from Chemical Combinatorial Libraries". W Methods of Biochemical Analysis, 259–67. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9780470939932.ch10.
Pełny tekst źródłade Berg, Kevin C. "The Reaction: Chemical Affinity and Controversy". W The Iron(III) Thiocyanate Reaction, 31–39. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-27316-3_4.
Pełny tekst źródłaSato, Tsutomu. "Chemical Affinity in Kant’s Practical Philosophy". W Law and Peace in Kant’s Philosophy, 359–68. Berlin, New York: Walter de Gruyter, 2008. http://dx.doi.org/10.1515/9783110210347.3.359.
Pełny tekst źródłaWang, Guangquan, Jeffrey R. Salm, Patrick V. Gurgel i Ruben G. Carbonell. "Small Peptide Ligands for Affinity Separations of Biological Molecules". W Chemical Engineering, 63–83. Chichester, UK: John Wiley & Sons, Ltd, 2005. http://dx.doi.org/10.1002/0470025018.ch3.
Pełny tekst źródłaAdamczewski, Martin, i Jean-Pierre Kinet. "The High-Affinity Receptor for Immunoglobulin E". W Chemical Immunology and Allergy, 173–90. Basel: KARGER, 1994. http://dx.doi.org/10.1159/000319254.
Pełny tekst źródłaYatsimirsky, Anatoly K., i Vladimir M. Mirsky. "Quantitative Affinity Data on Selected Artificial Receptors". W Artificial Receptors for Chemical Sensors, 439–60. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527632480.ch14.
Pełny tekst źródłaTakayama, Hiroshi, Takashi Moriya i Naoki Kanoh. "Preparation of Photo-Cross-Linked Small Molecule Affinity Matrices for Affinity Selection of Protein Targets for Biologically Active Small Molecules". W Chemical Genomics and Proteomics, 75–83. Totowa, NJ: Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-349-3_6.
Pełny tekst źródłaMirsky, Vladimir M. "Quantitative Characterization of Affinity Properties of Immobilized Receptors". W Artificial Receptors for Chemical Sensors, 1–15. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527632480.ch1.
Pełny tekst źródłaCodd, Rachel, Jiesi Gu, Najwa Ejje i Tulip Lifa. "New Applications of Immobilized Metal Ion Affinity Chromatography in Chemical Biology". W Inorganic Chemical Biology, 1–35. Chichester, UK: John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118682975.ch1.
Pełny tekst źródłaGutsev, G. L., i A. I. Boldyrev. "The Theoretical Investigation of the Electron Affinity of Chemical Compounds". W Advances in Chemical Physics, 169–221. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470142851.ch3.
Pełny tekst źródłaStreszczenia konferencji na temat "Chemical affinity"
Weaver, John B., i Adam M. Rauwerdink. "Chemical binding affinity estimation using MSB". W SPIE Medical Imaging, redaktorzy John B. Weaver i Robert C. Molthen. SPIE, 2011. http://dx.doi.org/10.1117/12.878788.
Pełny tekst źródła"Estrogen receptor binding affinity estimated by QSAR". W International Institute of Chemical, Biological & Environmental Engineering. International Institute of Chemical, Biological & Environmental Engineering, 2015. http://dx.doi.org/10.15242/iicbe.c0615100.
Pełny tekst źródłaFreidin, Alexander B. "Chemical Affinity Tensor and Stress-Assist Chemical Reactions Front Propagation in Solids". W ASME 2013 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/imece2013-64957.
Pełny tekst źródłaYang, Yin-Jie, Ellis M. Shelley, Yi-Chia Liaw, Shing-Yi Suen, Min-Ying Wang, Eric D. Conte, Tai-Hong Cheng, Cheng-Chiang Huang i Shin-Ying Chou. "Preparation of Polyacrylonitrile-based Immobilized Metal-Ion Affinity Membrane for Protein Adsorption". W 14th Asia Pacific Confederation of Chemical Engineering Congress. Singapore: Research Publishing Services, 2012. http://dx.doi.org/10.3850/978-981-07-1445-1_304.
Pełny tekst źródłaYang, Shiau-Jyun, i Yu-Kaung Chang. "Method Development for Extraction of GST-EGFP Fusion Protein by Immobilized Metal Affinity Chromatography". W 14th Asia Pacific Confederation of Chemical Engineering Congress. Singapore: Research Publishing Services, 2012. http://dx.doi.org/10.3850/978-981-07-1445-1_714.
Pełny tekst źródłaVijayakumaran, Thivina, U. Hashim, A. Rahim Ruslinda, M. K. Arshad, P. Veeradasan i N. K. S. Nordin. "Improving the affinity of silicon surface for biosensor application: The interaction between multiwall carbon nanotube (MWCNT) and chitosan (CS)". W 11TH ASIAN CONFERENCE ON CHEMICAL SENSORS: (ACCS2015). Author(s), 2017. http://dx.doi.org/10.1063/1.4975294.
Pełny tekst źródłaChou, Yan-Syun, i Yu-kaung Chang. "Stirred Fluidized Bed Immobilized Metal Affinity Chromatography for Direct Recovery of Poly His-tagged Enhanced Green Fluorescent Protein". W 14th Asia Pacific Confederation of Chemical Engineering Congress. Singapore: Research Publishing Services, 2012. http://dx.doi.org/10.3850/978-981-07-1445-1_709.
Pełny tekst źródłaNa Luo, Wei Feng, Xiaoqiang Wang i Feng Qian. "Dynamic optimization of chemical engineering problems using affinity propagation based estimation of distribution algorithm". W 2014 11th World Congress on Intelligent Control and Automation (WCICA). IEEE, 2014. http://dx.doi.org/10.1109/wcica.2014.7053323.
Pełny tekst źródłaMosentsova, K. I., A. V. Toropova, M. Nour, A. Eldeeb i D. M. Kolpashchikov. "DEPENDENCE OF THE AFFINITY OF OLIGONUCLEOTIDES ON CHEMICAL MODIFICATIONS AND THE LENGTH OF NUCLEOTIDE SEQUENCES". W X Международная конференция молодых ученых: биоинформатиков, биотехнологов, биофизиков, вирусологов и молекулярных биологов — 2023. Novosibirsk State University, 2023. http://dx.doi.org/10.25205/978-5-4437-1526-1-278.
Pełny tekst źródłaCHEN, KUAN, i THOMAS EDDY. "Investigation of chemical affinity for reacting flows of non-LThE (non-Local Thermal Equilibrium) gases". W 24th Plasma Dynamics, and Lasers Conference. Reston, Virigina: American Institute of Aeronautics and Astronautics, 1993. http://dx.doi.org/10.2514/6.1993-3225.
Pełny tekst źródłaRaporty organizacyjne na temat "Chemical affinity"
Glasscott, Matthew, Johanna Jernberg, Erik Alberts i Lee Moores. Toward the electrochemical detection of 2,4-dinitroanisole (DNAN) and pentaerythritol tetranitrate (PETN). Engineer Research and Development Center (U.S.), marzec 2022. http://dx.doi.org/10.21079/11681/43826.
Pełny tekst źródłaAuthor, Not Given. Colloids in groundwater: Their mobilization, subsurface transport, and sorption affinity for toxic chemicals. Office of Scientific and Technical Information (OSTI), styczeń 1991. http://dx.doi.org/10.2172/6144063.
Pełny tekst źródłaGschwend, P. M. Colloids in groundwater: Their mobilization, subsurface transport, and sorption affinity for toxic chemicals. Office of Scientific and Technical Information (OSTI), lipiec 1992. http://dx.doi.org/10.2172/7288440.
Pełny tekst źródłaChen, Yona, Jeffrey Buyer i Yitzhak Hadar. Microbial Activity in the Rhizosphere in Relation to the Iron Nutrition of Plants. United States Department of Agriculture, październik 1993. http://dx.doi.org/10.32747/1993.7613020.bard.
Pełny tekst źródłaGschwend, P. M. Colloids in groundwater: Their mobilization, subsurface transport, and sorption affinity for toxic chemicals. Annual technical progress report. Office of Scientific and Technical Information (OSTI), lipiec 1992. http://dx.doi.org/10.2172/10168896.
Pełny tekst źródłaChefetz, Benny, Baoshan Xing i Yona Chen. Interactions of engineered nanoparticles with dissolved organic matter (DOM) and organic contaminants in water. United States Department of Agriculture, styczeń 2013. http://dx.doi.org/10.32747/2013.7699863.bard.
Pełny tekst źródłaAvnimelech, Yoram, Richard C. Stehouwer i Jon Chorover. Use of Composted Waste Materials for Enhanced Ca Migration and Exchange in Sodic Soils and Acidic Minespoils. United States Department of Agriculture, czerwiec 2001. http://dx.doi.org/10.32747/2001.7575291.bard.
Pełny tekst źródłaLandau, Sergei Yan, John W. Walker, Avi Perevolotsky, Eugene D. Ungar, Butch Taylor i Daniel Waldron. Goats for maximal efficacy of brush control. United States Department of Agriculture, marzec 2008. http://dx.doi.org/10.32747/2008.7587731.bard.
Pełny tekst źródłaShomer, Ilan, Ruth E. Stark, Victor Gaba i James D. Batteas. Understanding the hardening syndrome of potato (Solanum tuberosum L.) tuber tissue to eliminate textural defects in fresh and fresh-peeled/cut products. United States Department of Agriculture, listopad 2002. http://dx.doi.org/10.32747/2002.7587238.bard.
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