Literatura académica sobre el tema "Chromatographic assays"
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Artículos de revistas sobre el tema "Chromatographic assays"
Ristuccia, Patricia A. "Liquid Chromatographic Assays of Antimicrobial Agents". Journal of Liquid Chromatography 10, n.º 2-3 (febrero de 1987): 241–76. http://dx.doi.org/10.1080/01483918708066718.
Texto completoReif, Van D., Kevin L. Kaufmann, Nicholas J. Deangelis y Mary C. Frankhouser. "Liquid Chromatographic Assays for Barbiturate Injections". Journal of Pharmaceutical Sciences 75, n.º 7 (julio de 1986): 714–16. http://dx.doi.org/10.1002/jps.2600750721.
Texto completoZhao, Qiang, Xing-Fang Li, Yuanhua Shao y X. Chris Le. "Aptamer-Based Affinity Chromatographic Assays for Thrombin". Analytical Chemistry 80, n.º 19 (octubre de 2008): 7586–93. http://dx.doi.org/10.1021/ac801206s.
Texto completoTurpeinen, U., P. Lehtovirta, H. Alfthan y U. H. Stenman. "Interference by human anti-mouse antibodies in CA 125 assay after immunoscintigraphy: anti-idiotypic antibodies not neutralized by mouse IgG but removed by chromatography". Clinical Chemistry 36, n.º 7 (1 de julio de 1990): 1333–38. http://dx.doi.org/10.1093/clinchem/36.7.1333.
Texto completoWilliard, Clark V. "Bioanalytical method transfer considerations of chromatographic-based assays". Bioanalysis 8, n.º 13 (julio de 2016): 1409–13. http://dx.doi.org/10.4155/bio.16.34.
Texto completoJohns, Margaret A., Laura K. Rosengarten, Martha Jackson y Fred E. Regnier. "Enzyme-linked immunosorbent assays in a chromatographic format". Journal of Chromatography A 743, n.º 1 (agosto de 1996): 195–206. http://dx.doi.org/10.1016/0021-9673(96)00370-6.
Texto completoLondhe, Vaishali y Madhura Rajadhyaksha. "Review of Recommendations for Bioanalytical Method Validation: Chromatographic Assays and Ligand Binding Assays". Chromatographia 82, n.º 2 (19 de diciembre de 2018): 523–35. http://dx.doi.org/10.1007/s10337-018-3677-z.
Texto completoColeman, Mark R., Thomas D. Macy, John W. Morgan y J. Matthew Rodewald. "Ruggedness of the Monensin and Narasin Liquid Chromatographic Assays". Journal of AOAC INTERNATIONAL 77, n.º 5 (1 de septiembre de 1994): 1065–72. http://dx.doi.org/10.1093/jaoac/77.5.1065.
Texto completoVidal-Casanella, Oscar, Javier Moreno-Merchan, Merce Granados, Oscar Nuñez, Javier Saurina y Sonia Sentellas. "Total Polyphenol Content in Food Samples and Nutraceuticals: Antioxidant Indices versus High Performance Liquid Chromatography". Antioxidants 11, n.º 2 (7 de febrero de 2022): 324. http://dx.doi.org/10.3390/antiox11020324.
Texto completoMoraes, Marcela Cristina, Carmen Cardoso, Cláudia Seidl, Ruin Moaddel y Quezia Cass. "Targeting Anti-Cancer Active Compounds: Affinity-Based Chromatographic Assays". Current Pharmaceutical Design 22, n.º 39 (14 de diciembre de 2016): 5976–87. http://dx.doi.org/10.2174/1381612822666160614080506.
Texto completoTesis sobre el tema "Chromatographic assays"
Serrano, Nadja Fernanda Gonzaga. "Produção de compostos antimicrobianos por Paenibacillus polymyxa RNC-D: otimização das condições de cultivo, purificação e caracterização dos bioprodutos". Universidade Federal de São Carlos, 2014. https://repositorio.ufscar.br/handle/ufscar/273.
Texto completoFinanciadora de Estudos e Projetos
The increase in the production of antimicrobial metabolites by Paenibacillus polymyxa RNC-D was appraised through the study of cultivation variables. Two process variables, namely the glucose and inoculum concentrations, were evaluated in different levels (5 to 40 g/l, and 2.5% to 5.0% v/v, respectively), and their effects on biomass formation, minimal inhibitory concentration (MIC) against Escherichia coli and surface tension reduction (STR) were studied. The fermentation process was firstly carried out using non-optimized parameters, where the dependent variables biomass, MIC and STR reached the values of 0.6 g/l, 1.000,0 μg/ml and 18.4 mN/m, respectively. The optimum glucose (16 g/l) and inoculum concentrations (5.0% v/v) were defined in order to maximize the biomass formation, with low value of MIC and large STR of extract. Under these conditions, a biomass of 2.76 g/l, MIC of 15.8 μg/ml, and STR of 14.58 mN/m were predicted by the model. Data attained by experiments using optimized settings showed the following values: biomass 2.05 g/l; MIC 31.2 μg/ml; STR 10.7 mN/m. Thus, the percentage of improvement for each target response was: biomass 241.6%; MIC 96.88%; STR 41.85%. It was found that high concentrations of glucose substrate, although reflected in an increase in bacterial biomass, inhibited the microbial secondary metabolism, resulting in a low production of biomolecules associated with high values of MICs. Thus, initial concentrations of glucose and inoculum are shown as variables of strong influence in the production of antimicrobial metabolites by P. polymyxa RNC-D. Through the methods of experimental factorial design and surfaceresponse followed by graphical optimization it was possible to determine the optimum operating condition to achieve both maximum biomass and RTS as well as and lowest possible values of CIM. The validity of the proposed model was verified and confirmed. This is the first study on the optimization of culture conditions for the production of antimicrobial metabolites by P. polymyxa RNC-D, and constitutes an important step in the development of strategies to modulate the production of antimicrobial molecules by this microorganism in elevated levels. Novel antimicrobial compounds were isolated from the fermentation broth of P. polymyxa RNC-D, here named total extract (TE). It was possible to verify the presence of lipopeptide and peptide active compounds through enzymatic assays made with ET. Total extract was subjected to a two-phase system, resulting in lipopeptide extract (LPE) and aqueous fraction (AF). According to the results of bioassays, LPE has broad-spectrum activity against Gram-positive bacteria, Gram-negative bacteria and fungi. The mass spectrometry analysis of PLA revealed the existence of a novel compound that was named polycerradin. The purification of a novel antimicrobial peptide (AMP) from the AF was carried out by using chromatography. The compound was active against Gram-negative bacteria. Nterminal analysis determined the amino acid sequence, as well as MS / MS analysis confirmed the primary structure of this new compound. This research reports firstly the production of PAM PpRNCD that has an unusual amino acid in its constitution. It is an unprecedented fact considering the bacterial specie P. polymyxa. In terms of molecule size, PAM PpRNCD can be considered one of the smallest active natural peptide reported to date. It was also possible to isolate from FA the depsipeptides IL-F04a (m/z 883), LI-F04b (m/z 897), LI-F03a (m/z 947) and LI-F03b (m/z 961) previously described in the literature. The photoluminescence study of the LPE, TE, AF in both at room temperature (RT) and low temperature (T = 8K) was performed. In addition, this technique was applied to evaluate the action of the ELP on Staphylococcus aureus ATCC 29213, Enterococcus faecalis ATCC 29212, Escherichia coli ATCC 29212, Shigella sonnei ATCC 1578 and Candida albicans ATCC 10231 in two different situations: (a) immediately after mixing LPE with the bacterial and fungus cell suspension, and (b) after thirty minutes. The photoluminescence emission was collected by a triple spectrometer (three diffraction gratings) T64000 model from Jobin Yvon, equipped with an optical microscope. For the detection of the radiation emitted by the sample we used a CCD camera (charge coupled device) cooled by liquid nitrogen. The slits of the spectrometer were adjusted to produce a spectral resolution of the order of 10-4 nm. The excitation source used was the line of 457 nm (violet) from an argon laser. The behaviors here observed indicate a strong potential for applications in biosensors as well as molecular markers.
Através do estudo de variáveis do cultivo pretendeu-se aumentar a produção de metabólitos antimicrobianos por Paenibacillus polymyxa RNC-D. Duas variáveis do processo - glicose e concentração de inóculo - foram avaliadas em diferentes níveis e seus efeitos na formação de biomassa, concentração inibitória mínima (CIM) contra Escherichia coli e redução na tensão superficial (RTS) foram estudados. Utilizando parâmetros não-otimizados as variáveis dependentes biomassa, CIM e RTS atingiram valores de 0,6 g/l, 1.000,0 μg/ml e 18,4 mN/m, respectivamente. As concentrações ótimas de glicose (16 g/l) e inóculo (5,0% v/v) foram definidas no sentido de maximizar a formação de biomassa e RTS do extrato, bem como diminuir o valor de CIM do extrato. Experimentalmente 2,05 g/l de biomassa; 31,2 μg/ml de CIM e 10,7 mN/m de RTS foram obtidos sob condições otimizadas. Foi constatado que altas concentrações do substrato glicose, embora refletissem em aumento de biomassa bacteriana, inibiram o metabolismo secundário microbiano, resultando em baixa produção de biomoléculas associada a altos valores de CIM. Através dos métodos de design fatorial experimental e superfície-resposta seguidos por otimização gráfica foi possível determinar a condição operacional ótima das concentrações iniciais de glicose e inóculo, as quais se demonstraram como variáveis de grande influência na produção de metabólitos antimicrobianos por P. polymyxa RNC-D. O extrato total (ET), proveniente do caldo de fermentação de P. polymyxa RNC-D, foi utilizado para pesquisa e isolamento de novos compostos antimicrobianos. Através de ensaios enzimáticos feitos com ET foi possível verificar a natureza lipopeptídica e peptídica dos compostos antimicrobianos. O ET foi submetido a um sistema de duas fases, separandose então em extrato lipopeptídico (ELP) e fração aquosa (FA). Resultados de bioensaios revelaram que o ELP apresenta amplo espectro de atividade contra bactérias Grampositivas, Gram-negativas e fungo. A análise por espectrometria de massas de ELP revelou a presença de um composto peptídico inédito o qual foi denominado polycerradin. A partir da fração aquosa (FA) foi possível a purificação de um novo peptídeo antimicrobiano (PAM) através de etapas cromatográficas. A bioatividade do composto foi avaliada e confirmada frente às bactérias Gram-negativas. A determinação da sequência de aminoácidos foi realizada por análise do N-terminal, e a confirmação da estrutura primária deste novo composto foi feita por MS/MS. O presente estudo relata pela primeira vez a produção do PAM PpRNCD que possui um aminoácido não usual em sua constituição, relato primeiramente aqui descrito considerando-se a espécie bacteriana P. polymyxa. Em termos de tamanho de molécula, pode-se considerar que o PAM PpRNCD é um dos menores peptídeos naturais ativos relatados até o momento. Utilizando-se a FA também foi possível o isolamento dos depsipeptídeos LI-F04a (m/z 883), LI-F04b (m/z 897), LI-F03a (m/z 947) e LI-F03b (m/z 961) previamente descritos na literatura. O estudo da fotoluminescência do ELP, do ET e da FA foi realizado tanto em temperatura ambiente (RT) quanto em baixa temperatura (T=8K). Também se estudou, através desta técnica, a ação do ELP sobre as bactérias Staphylococcus aureus ATCC 29213, Enterococcus faecalis ATCC 29212, Escherichia coli ATCC 29212, Shigella sonnei ATCC 1578 e fungo Candida albicans ATCC 10231 em duas situações: (a) imediatamente após a mistura do ELP com a suspensão celular bacteriana, e (b) trinta minutos após a mistura. Detectou-se emissão fotoluminescente por ELP, ET e FA, e sinais de Raman a λ 699 nm (FA a baixa temperatura). Decorridos 30 min da mistura do ELP com as suspensões celulares microbianas houve alteração na emissão fotoluminescente, sendo que alguns sinais foram suprimidos (λ 470, 480 e 700 nm para S. sonnei, por exemplo). Isto evidencia a potencial aplicação destas frações (ELP, ET e FA) para a fabricação de sensores, detectores e marcadores moleculares.
Zhang, Qunying. "Characterization of receptors for Escherichia coli 987P using competitive binding assays, thin-layer chromatography and gel filtration chromatography". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape2/PQDD_0023/MQ51825.pdf.
Texto completoEmbree, Leanne. "Development of a high-performance liquid chromatographic assay for human chorionic gonadotropin as an alternative to the official United States pharmacopeial animal assay". Thesis, University of British Columbia, 1985. http://hdl.handle.net/2429/24637.
Texto completoPharmaceutical Sciences, Faculty of
Graduate
Fillmann, Gilberto. "Appraisal and validation of rapid, integrated chemical and biological assays of environmental quality". Thesis, University of Plymouth, 2001. http://hdl.handle.net/10026.1/2372.
Texto completoAhmed, Naila Masud. "Chromatographic assay of advanced glycation endproducts and application to the study of human disease". Thesis, University of Essex, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.364507.
Texto completoBhattacharjee, Rathindra Chandra. "Development of a sensitive and stereoselective high performance liquid chromatographic assay method for propafenone enantiomers in human plasma". Thesis, University of British Columbia, 1988. http://hdl.handle.net/2429/27800.
Texto completoPharmaceutical Sciences, Faculty of
Graduate
CHILAKALA, SUJATHA. "DEVELOPMENT OF LIQUID CHROMATOGRAPHY-MASS SPECTROMETRIC ASSAYS AND SAMPLE PREPARATION METHODS FOR THE BIOLOGICAL SAMPLE ANALYSIS". Cleveland State University / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=csu1512927043412916.
Texto completoLövgren, Ulf. "Enzyme immunoassay in combination with liquid chromatography for sensitive and selective determination of drugs in biosamples". Lund : Dept. of Analytical Chemistry, Lund University, 1997. http://books.google.com/books?id=Ju1qAAAAMAAJ.
Texto completoKirk, Loren Madden y Stacy D. Brown. "Beyond-Use Date Determination of Buprenorphine Buccal Solution Using a Stability-Indicating High-Performance Liquid Chromatographic Assay". Digital Commons @ East Tennessee State University, 2015. https://dc.etsu.edu/etsu-works/5305.
Texto completoLiu, Tina. "Development and validation of an HPLC assay for simethicone in pharmaceutical formulations". Master's thesis, Department of Pharmacy, 2001. http://hdl.handle.net/2123/12307.
Texto completoLibros sobre el tema "Chromatographic assays"
High performance liquid chromatography in enzymatic analysis: Applications to the assay of enzymatic activity. New York: Wiley, 1987.
Buscar texto completoRossomando, Edward F. High performance liquid chromatography in enzymatic analysis: Applications to the assay of enzymatic activity. New York: Wiley, 1987.
Buscar texto completoChiappetta, Terasa. Comparison of microbiological assay with spectrophotometry and high-performance liquid chromatography in the quantitative analysis of gentamicin spiked in phosphate buffered saline. Sudbury, Ont: Laurentian University, 2004.
Buscar texto completoGolubkina, Nadezhda, Elena Kekina, Anna Molchanova y Sergey Nadezhkin. Antioxidants of plants and methods of their definition. ru: INFRA-M Academic Publishing LLC., 2020. http://dx.doi.org/10.12737/1045420.
Texto completoVandenBoer, Trevor. Development of an analysis for ketamine in wistar rat femoral bone, bone marrow and blood following a single acute administration by enzyme-linked immunosorbent assay and gas chromatography electron capture detection methods. Sudbury, Ont: Laurentian University, 2007.
Buscar texto completoGerman, Igor. Ultrasensitive detection of proteins and peptides by capillary electrophoresis affinity assays. 2001.
Buscar texto completoTargove, Margaret Alice. Post-column chemiluminescent detection of pharmaceuticals and direct or indirect electrochemical detection using a carbon paste electrode with high performance liquid chromatography. 1988.
Buscar texto completoPuntis, John. Carbohydrate intolerance. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198759928.003.0020.
Texto completoNewman, Franklin Scott. Comparison of the Chromatographic and the Microbiological Assay Methods for the Determination of the Nucleic Acids in Newcastle Virus. Creative Media Partners, LLC, 2021.
Buscar texto completoStill, Rachel. Evaluation of a high performance liquid chromatography assay for measurement of plasma homocysteine, with application to patients with suspected vitamin B12 or folate deficiency. 1996.
Buscar texto completoCapítulos de libros sobre el tema "Chromatographic assays"
Svinarov, D. A. "Unified Liquid Chromatographic and Gas Chromatographic Assays for Therapeutic Drug Monitoring and Toxicology". En Recent Developments in Therapeutic Drug Monitoring and Clinical Toxicology, 691–702. Boca Raton: CRC Press, 2023. http://dx.doi.org/10.1201/9781003418153-107.
Texto completoWainer, Irving W. "Developing Stereoselective High-Performance Liquid Chromatographic Assays for Pharmacokinetic Studies". En ACS Symposium Series, 100–110. Washington, DC: American Chemical Society, 1992. http://dx.doi.org/10.1021/bk-1992-0512.ch008.
Texto completoBall, G. F. M. "High-performance liquid chromatographic methods for the determination of thiamin, riboflavin, niacin, vitamin B6 folate and vitamin C". En Water-soluble Vitamin Assays in Human Nutrition, 202–316. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4615-2061-0_6.
Texto completoHonour, John W. "Gas Chromatography-Mass Spectrometry". En Hormone Assays in Biological Fluids, 53–74. Totowa, NJ: Humana Press, 2006. http://dx.doi.org/10.1385/1-59259-986-9:53.
Texto completoSchmidt, Dietmar. "Bioanalytical Assays – Gas Chromatography". En Drug Discovery and Evaluation, 629–42. Berlin, Heidelberg: Springer Berlin Heidelberg, 2006. http://dx.doi.org/10.1007/3-540-29804-5_34.
Texto completoSánchez-Guijo, Alberto, Michaela F. Hartmann y Stefan A. Wudy. "Introduction to Gas Chromatography-Mass Spectrometry". En Hormone Assays in Biological Fluids, 27–44. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-616-0_3.
Texto completoHonour, John W. "High-Performance Liquid Chromatography for Hormone Assay". En Hormone Assays in Biological Fluids, 25–52. Totowa, NJ: Humana Press, 2006. http://dx.doi.org/10.1385/1-59259-986-9:25.
Texto completoSchmidt, Dietmar. "Bioanalytical Assays: Gas Chromatography (GC)". En Drug Discovery and Evaluation: Safety and Pharmacokinetic Assays, 835–52. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-25240-2_34.
Texto completoSchmidt, Dietmar. "Bioanalytical Assays: Gas Chromatography (GC)". En Drug Discovery and Evaluation: Safety and Pharmacokinetic Assays, 1–19. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-73317-9_34-1.
Texto completoNeubert, Hendrik. "Quantification of Protein Biomarkers Using Liquid Chromatography Tandem Mass Spectrometry". En Translating Molecular Biomarkers into Clinical Assays, 87–98. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-40793-7_9.
Texto completoActas de conferencias sobre el tema "Chromatographic assays"
Lee, C. H. y A. Lal. "Low-Voltage High-Speed Ultrasonic Chromatography for Microfluidic Assays". En 2002 Solid-State, Actuators, and Microsystems Workshop. San Diego, CA USA: Transducer Research Foundation, Inc., 2002. http://dx.doi.org/10.31438/trf.hh2002.25.
Texto completoZhao, Ming, Dakang Ma, Quanxu Shen y Bin Hong. "Abstract 400: Immunofluorescence chromatographic assay of tumor cells in dried blood spot". En Proceedings: AACR 107th Annual Meeting 2016; April 16-20, 2016; New Orleans, LA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.am2016-400.
Texto completoYAMADA, K., T. MEGURO, A. SHIRAHATA, T. NAKAMURA y A. ASAKURA. "EFFECTS OF VITAMIN K ON VITAMIN K DEPENDENT PROTEINS IN NEWBORN INFANTS". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644264.
Texto completoHori, F. y S. Uno. "Electrochemical Impedance Spectroscopy of Colloidal Gold Nanoparticles in Chromatography Paper for Immunochromatographic Assay". En 2014 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2014. http://dx.doi.org/10.7567/ssdm.2014.ps-11-14.
Texto completoHeiremans, J., M. Claeys y A. G. Herman. "DETERMINATION OF CHOLESTERYL HYDROXYOCTADBCADIENOATES IN VASCULAR TISSUE BY HPLC AND ITS RELEVANCE TO ATHEROSCLEROSIS". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643084.
Texto completoRiethorst, W., M. W. P. M. te Booy, T. Beugeling, A. Bantjes, J. Over y W. G. van Aken. "THE ISOLATION OF COAGULATION FACTOR VIII FROM HUMAN BLOOD PLASMA BY AFFINITY CHROMATOGRAPHY". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644059.
Texto completoTandon, N. N. y G. A. Jamieson. "ROLE OF PLATELET MEMBRANE GLYCOPROTEIN IV IN PLATELET-COLLAGEN INTERACTION: A MICROTITER ASSAY TO STUDY PLATELET ADHERENCE". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643906.
Texto completoGiddings, J. C. "AN IMMUNORADIOMETRIC ASSAY (IRMA) FOR HUMANTHROMBOMODULIN". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643963.
Texto completoLin, Hongxia, Murugesan K. Gounder, Susan Goodin, Joseph R. Bertino, Robert S. DiPaola y Roger K. Strair. "Abstract 2759: Validated liquid chromatography-mass spectrometry assay for determination of busulfan: Application to clinical pharmacokinetics studies". En Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-2759.
Texto completoGRIFFITH, M., S. A. LIU, G. NESLUND, I. TSANG, D. LETTELIER y R. BERKEBILE. "PREPARATION OF HIGH SPECIFIC ACTIVITY PLASMA AHF BY ANTI-FVIIIc IMMUNOAFFINITY CHROMATOGRAPHY". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643922.
Texto completoInformes sobre el tema "Chromatographic assays"
Olsen y Wise. PR-179-12603-R02 Energy Meter Performance Assessment Phase 1 Amendment - Unblinded. Chantilly, Virginia: Pipeline Research Council International, Inc. (PRCI), abril de 2014. http://dx.doi.org/10.55274/r0010833.
Texto completoOlsen y Wise. PR-179-12603-R03 Energy Meter Performance Assessment Phase 1 Amendment - Blinded. Chantilly, Virginia: Pipeline Research Council International, Inc. (PRCI), junio de 2014. http://dx.doi.org/10.55274/r0010559.
Texto completoBora. PR-004-14604-R01 Miniaturized Gas Chromatography and Gas Quality Sensor. Chantilly, Virginia: Pipeline Research Council International, Inc. (PRCI), junio de 2015. http://dx.doi.org/10.55274/r0010869.
Texto completoPeterson, Warren. PR-663-19600-Z01 Develop Guidance for Calculation of HCDP in Pipelines. Chantilly, Virginia: Pipeline Research Council International, Inc. (PRCI), marzo de 2020. http://dx.doi.org/10.55274/r0011659.
Texto completoMoores, Lee C., P. U. Ashvin, I. Fernando y Garret W. George. Synthesis of 2-Methoxypropyl Benzene for Epitope Imprinting. U.S. Army Engineer Research and Development Center, julio de 2022. http://dx.doi.org/10.21079/11681/44883.
Texto completoAnnunziato, Dominick. HPLC Sample Prep and Extraction SOP v1.3 for Fungi. MagicMyco, agosto de 2023. http://dx.doi.org/10.61073/sopv1.3.08.11.2023.
Texto completoLee, S. W. Supercritical fluid chromatographic analysis of aromatic ring type component of diesel fuels for an engine testing program to assess impact of fuel aromatics on diesel emissions. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1993. http://dx.doi.org/10.4095/304569.
Texto completoHorton, David, Victoria Soroker, Peter Landolt y Anat Zada Byers. Characterization and Chemistry of Sexual Communication in Two Psyllid Pests of Pears (Homoptera: Psyllidae). United States Department of Agriculture, agosto de 2011. http://dx.doi.org/10.32747/2011.7592653.bard.
Texto completoBadrinarayanan y Olsen. PR-179-11201-R01 Performance Evaluation of Multiple Oxidation Catalysts on a Lean Burn Natural Gas Engine. Chantilly, Virginia: Pipeline Research Council International, Inc. (PRCI), agosto de 2012. http://dx.doi.org/10.55274/r0010772.
Texto completoFluhr, Robert y Maor Bar-Peled. Novel Lectin Controls Wound-responses in Arabidopsis. United States Department of Agriculture, enero de 2012. http://dx.doi.org/10.32747/2012.7697123.bard.
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