Relevant bibliographies by topics / CHLORINE 37

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers
  5. Reports

Academic literature on the topic 'CHLORINE 37'

Author: Grafiati
Published: 4 June 2021
Last updated: 5 February 2022

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Journal articles on the topic "CHLORINE 37"

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Wadsworth, Alan H., Steve Montgomery, Kenneth W. M. Lawrie, and Richard M. Carr. "Isotopic labelling with chlorine-37." Journal of Labelled Compounds and Radiopharmaceuticals 50, no. 5-6 (2007): 471–72. http://dx.doi.org/10.1002/jlcr.1200.

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Chang, Yoon-Seok, and Max L. Deinzer. "Synthesis of Regiospecific Chlorine-37 Labeled Trichlorodibenzofuran." Synthetic Communications 20, no. 16 (August 1990): 2501–6. http://dx.doi.org/10.1080/00397919008053199.

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CHANG, Y. S., and M. L. DEINZER. "ChemInform Abstract: Synthesis of Regiospecific Chlorine-37 Labeled Trichlorodibenzofuran." ChemInform 22, no. 12 (August 23, 2010): no. http://dx.doi.org/10.1002/chin.199112128.

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Chang, Yoon-Seok, and Max L. Deinzer. "Regiospecific synthesis of polychlorinated dibenzofurans with chlorine-37 excess." Journal of Labelled Compounds and Radiopharmaceuticals 29, no. 1 (January 1991): 43–62. http://dx.doi.org/10.1002/jlcr.2580290108.

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Chang, Yoon Seok, James A. Laramee, and Max L. Deinzer. "Regioselective chloride ion loss from chlorine-37 enriched polychlorodibenzofurans by negative ion mass spectrometry." Analytical Chemistry 63, no. 23 (December 1991): 2715–18. http://dx.doi.org/10.1021/ac00023a010.

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Schaefer, Ted, and Rudy Sebastian. "Chlorine-37/chlorine-35 isotope effects on the proton NMR spectra of some chloromethane derivatives. Practical consequences." Journal of the American Chemical Society 109, no. 21 (October 1987): 6508–9. http://dx.doi.org/10.1021/ja00255a044.

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Iba, Yoshihisa, Fumiaki Kumasaka, Masayuki Takeda, Hajime Aoyama, and Masaki Yamabe. "Etching Residues of Sputtered Ta Film Using Chlorine-Based Plasma." Japanese Journal of Applied Physics 37, Part 2, No. 2B (February 15, 1998): L251—L254. http://dx.doi.org/10.1143/jjap.37.l251.

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Heineking, N., M. Andolfatto, U. Keussen, A. Mues, and H. Dreizler. "Deuterium Quadrupole Coupling Constants in Deuterochloroacetylene." Zeitschrift für Naturforschung A 44, no. 8 (August 1, 1989): 735–37. http://dx.doi.org/10.1515/zna-1989-0809.

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Abstract The deuterium and chlorine nuclear quadrupole coupling constants have been determined for both of the chlorine isotopomers of deuterochloroacetylene (DCCC1), along with the rotational, centrifugal distortion, and chlorine spin-rotation coupling constants. The values are B = 5186.97631 (22) MHz, DJ= 1.13(2) kHz, eQq(Cl)= -79.7358(19) MHz, cI(Cl) = 1.10(31)kHz, and eQq(D) = 207.0(28)kHz for DCCCl-35, and B = 5084.17839(30) MHz, DJ = 0.99(2) kHz, eQq(Cl)= -62.8451(27) MHz, cI(CI) = 0.76(43) kHz, and eQq(D) = 205.8(39)kHz for DCCCl-37.
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Amrute, Amol P., Gastón O. Larrazábal, Cecilia Mondelli, and Javier Pérez-Ramírez. "Titelbild: CuCrO2Delafossite: A Stable Copper Catalyst for Chlorine Production (Angew. Chem. 37/2013)." Angewandte Chemie 125, no. 37 (August 12, 2013): 9763. http://dx.doi.org/10.1002/ange.201306290.

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Vahala, R., V. A. Långvik, and R. Laukkanen. "Controlling Adsorbable Organic Halogens (AOX) and Trihalomethanes (THM) Formation by Ozonation and Two-Step Granule Activated Carbon (GAC) Filtration." Water Science and Technology 40, no. 9 (November 1, 1999): 249–56. http://dx.doi.org/10.2166/wst.1999.0488.

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A pilot plant study in four parallel filter runs was performed in order to determine the effect of ozonation and two-step granular activated carbon (GAC) filtration on the removal of disinfection by-product (DBP) precursors. The results showed that ozonation significantly decreased the adsorbable organic halogens (AOX) (35%), simulated distribution system (SDS) AOX (37%) and SDS trihalomethanes (THM) (76%) from chemically treated and sand-filtered lake water, but did not decrease either short-term or the long-term chlorine demand. Biofiltration with exhausted GAC had a minor importance in the precursor removal (0-20%). The performance of adsorptive GAC filtration was strongly dependent on the age of the GAC filter bed, which was also seen as a strong correlation between the natural organic matter (NOM) measurements and DBP formation potential. Disinfection with chloramine produced lower THM, AOX, mutagenicity and MX (Z-3-chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone) levels compared to chlorine disinfection.
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Dissertations / Theses on the topic "CHLORINE 37"

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Blondel, Antoine. "Effets de la température et de l’irradiation sur le comportement du chlore 37 dans le graphite nucléaire : conséquences sur la mobilité du chlore 36 dans les graphites irradiés." Thesis, Lyon 1, 2013. http://www.theses.fr/2013LYO10323/document.

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Ce travail s'inscrit dans le cadre des études sur la gestion des déchets graphités issus du démantèlement des centrales UNGG (Uranium Naturel Graphite Gaz). Les déchets graphités contiennent, entre autres, du 36Cl, radionucléide de longue période dimensionnant pour le stockage, car très mobile dans les ouvrages cimentaires et formations argileuses. Or, à ce jour, peu de données sont disponibles sur la localisation du 36Cl et sa spéciation dans le graphite nucléaire irradié. Ces informations sont nécessaires pour le dimensionnement d'un site de stockage adapté aux déchets graphités et leur obtention constitue l'objectif de ma thèse, réalisée en partenariat avec EDF, CEA et Andra. Dans ce contexte, nous avons mis en oeuvre des études expérimentales permettant de simuler et d'évaluer l'impact de la température, de l'irradiation et de la radiolyse à l'interface gaz/graphite sur le comportement en réacteur du 36Cl. La présence de 36Cl dans le graphite est simulée par l'implantation ionique de 37Cl dans des échantillons de graphite nucléaire vierge ce qui permet de nous affranchir des contraintes liées à l'utilisation de graphite irradié. En extrapolant nos résultats aux déchets graphités, nos études sur les effets comparatifs de la température et de l'irradiation montrent que la température tend à appauvrir l'inventaire en chlore 36 des graphites irradiés et que l'irradiation en régime mixte, tel qu'elle a lieu dans les réacteurs UNGG, renforce cet effet d'appauvrissement
This thesis deals with the studies of the management of irradiated graphite wastes issued from the dismantling of the UNGG French reactors. This work focuses on the behavior of 36Cl. This radionuclide is mainly issued through the neutron activation of 35Cl by the reaction 35Cl(n, γ)36Cl, pristine chlorine being an impurity of nuclear graphite, present at the level of some at.ppm. 36Cl is a long lived radionuclide (about 300,000 years) and is highly soluble in water and mobile in concrete and clay. The solubilization of 36Cl is controlled by the water accessibility into irradiated graphite pores as well as by factors related to 36Cl itself such as its chemical speciation and its location within the irradiated graphite. Both speciation and chlorine location should strongly influence its behaviour and need to be taken into account for the choice of liable management options. However, data on radioactive chlorine features are difficult to assess in irradiated graphite and are mainly related to detection sensitivity problems. In this context, we simulated and evaluated the impact of the temperature, the irradiation and the radiolytic oxidation on the chlorine 36 behaviour. In order to simulate the presence of 36Cl, we implanted 37Cl into virgin nuclear graphite. Ion implantation has been widely used to study the lattice location, the diffusion and the release of fission and activation products in nuclear materials. Our results on the comparative effects of the temperature and the irradiation show that chlorine occurs in irradiated graphite on temperature and electronic and nuclear irradiation improve this effect
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Smith, Fiona Elizabeth. "Observation of the infrared spectrum of the doubly charged molecular ion D'3'7Cl'2'+." Thesis, University of Newcastle Upon Tyne, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.323488.

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Blondel, Antoine. "Effets de la température et de l'irradiation sur le comportement du chlore 37 dans le graphite nucléaire : Conséquences sur la mobilité du chlore 36 dans les graphites irradiés." Phd thesis, Université Claude Bernard - Lyon I, 2013. http://tel.archives-ouvertes.fr/tel-00951986.

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Ce travail s'inscrit dans le cadre des études sur la gestion des déchets graphités issus du démantèlement des centrales UNGG (Uranium Naturel Graphite Gaz). Les déchets graphités contiennent, entre autres, du 36Cl, radionucléide de longue période dimensionnant pour le stockage, car très mobile dans les ouvrages cimentaires et formations argileuses. Or, à ce jour, peu de données sont disponibles sur la localisation du 36Cl et sa spéciation dans le graphite nucléaire irradié. Ces informations sont nécessaires pour le dimensionnement d'un site de stockage adapté aux déchets graphités et leur obtention constitue l'objectif de ma thèse, réalisée en partenariat avec EDF, CEA et Andra. Dans ce contexte, nous avons mis en œuvre des études expérimentales permettant de simuler et d'évaluer l'impact de la température, de l'irradiation et de la radiolyse à l'interface gaz/graphite sur le comportement en réacteur du 36Cl. La présence de 36Cl dans le graphite est simulée par l'implantation ionique de 37Cl dans des échantillons de graphite nucléaire vierge ce qui permet de nous affranchir des contraintes liées à l'utilisation de graphite irradié. En extrapolant nos résultats aux déchets graphités, nos études sur les effets comparatifs de la température et de l'irradiation montrent que la température tend à appauvrir l'inventaire en chlore 36 des graphites irradiés et que l'irradiation en régime mixte, tel qu'elle a lieu dans les réacteurs UNGG, renforce cet effet d'appauvrissement
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Book chapters on the topic "CHLORINE 37"

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Sukhoruchkin, S. I., and Z. N. Soroko. "Neutron Resonance Parameters for Cl-37 (Chlorine)." In Supplement to Volume I/24, 267–75. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-45603-3_44.

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Sukhoruchkin, S. I., and Z. N. Soroko. "Excited Nuclear States for Cl-37 (Chlorine)." In Supplement to I/25 A-F, 1027–53. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-48875-1_160.

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Sukhoruchkin, S. I., and Z. N. Soroko. "Neutron Resonance Parameters for Cl-37 (Chlorine)." In Neutron Resonance Parameters, 364–74. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-87866-7_42.

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Sukhoruchkin, S. I., and Z. N. Soroko. "Excited Nuclear States for Cl-37 (Chlorine)." In Nuclei with Z = 1 - 29, 2128–31. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-22798-1_255.

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Sukhoruchkin, S. I., and Z. N. Soroko. "Excited Nuclear States for Cl-37 (Chlorine)." In Supplement to I/25 A-E, 752–66. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-47801-1_145.

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Sukhoruchkin, S. I., and Z. N. Soroko. "Atomic Mass and Nuclear Binding Energy for Cl-37 (Chlorine)." In Nuclei with Z = 1 - 54, 1106–8. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-69945-3_510.

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"Chlordane." In Toxicology Desk Reference, edited by Robert P. Ryan, Claude E. Terry, and Sanford S. Leffingwell, 301–7. Routledge, 2019. http://dx.doi.org/10.1201/9780203735398-37.

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Mogensen, Knud Erik, and Gilles Uzé. "[37] Radioiodination of human alpha interferons by the chloramine T method." In Methods in Enzymology, 267–76. Elsevier, 1986. http://dx.doi.org/10.1016/0076-6879(86)19039-2.

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Li, Jie Jack, Chris Limberakis, and Derek A. Pflum. "Functional Group Manipulations." In Modern Organic Synthesis in the Laboratory. Oxford University Press, 2008. http://dx.doi.org/10.1093/oso/9780195187984.003.0008.

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CBr4–Ph3P is very straightforward and widely used. Workup and purification can be messy at times because of the by-product, Ph3PO. To a mixture of the alcohol (0.800 g, 3.36 mmol) and carbon tetrabromide (1.337 g, 4.03 mmol) in CH2Cl2 at 0 ºC was added a solution of PPh3 (1.319 g, 5.03 mmol) in CH2Cl2 (3 mL). The reaction mixture was stirred at room temperature for 1 h, concentrated under reduced pressure, and purified by column chromatography to afford the bromide (0.941 g, 93% yield). Reference: Hu, T.-S.; Yu, Q.; Wu, Y.-L.; Wu, Y. J. Org. Chem. 2001, 66, 853–861. A two-step sequence consisting of mesylate formation followed by treatment with LiBr can also be used. This procedure involves two steps, but workup and purification are very straightforward. The bromide can be carried out to the next step without further purification in many cases. To a solution of 5-hydroxymethyl-1-methylcyclopentene (3.8 g, 34 mmol) in CH2 Cl2 (50 mL) at 0 ºC was added triethylamine (5.2 mL, 37 mmol) followed by methanesulfonyl chloride (2.9 mL, 37 mmol). The mixture was stirred at 0 ºC for 5 h and then water was added. The organic layer was separated and the aqueous layer was extracted with ether. The combined organic extracts were dried over MgSO4 and the solvent was removed under reduced pressure to give 6.4 g (98%) of (2-methylcyclopent-2- enyl)methyl methanesulfonate, which was used in the next step without further purification. A solution containing the mesylate (6.4 g, 34 mmol) in acetone (70 mL) was treated with lithium bromide (8.89 g, 102 mmol). The mixture was heated at reflux for 6 h, cooled to room temperature, diluted with water, extracted with ether, and the combined ethereal extracts were dried over MgSO4. Removal of the solvent under reduced pressure gave 4.6 g (78%) of 5-bromomethyl-1-methylcyclopentene, which was used in the next step without further purification.
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Magee, Patrick, and Mark Tooley. "Blood Gas Analysis." In The Physics, Clinical Measurement and Equipment of Anaesthetic Practice for the FRCA. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199595150.003.0021.

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A blood gas machine has electrodes to measure pH, pCO2 and pO2 and often measures Hb and some biochemistry as well [King et al. 2000]. Derived values from such a device include O2 saturation, O2 content, bicarbonate, base excess and total CO2. This is the Clarke electrode described in the previous section on gas analysers and is suitable for both respiratory and blood O2 analysis. A pH unit has been defined in Chapter 1 as. In words, this can be described as ‘the negative logarithm, to base ten, of the hydrogen ion concentration’. The physical principle on which the pH electrode is based depends on the fact that when a membrane separates two solutions of different [H+], a potential difference exists across the membrane. In a pH electrode, such a membrane is usually made of glass and the development of a potential difference between the two solutions is thought to be due to the migration of H+ into the glass matrix. If one solution consists of a standard [H+], the pH of the other solution can be estimated by measurement of the potential difference between them. The glass membrane used is selectively permeable to H+. No current flows in this device, which does not wear out, in contrast to the Clark electrode, in which current does flow and that does need periodic replacement. The pH measurement system is shown diagrammatically in Figure 17.1. It consists of two half cells. In one half it has an Ag/AgCl electrode and in the other a Hg/HgCl2 (calomel) electrode. Each electrode maintains a fixed electrical potential. The Ag/AgCl electrode is surrounded by a buffer solution of known pH, surrounded by the pH sensitive glass. Outside the glass membrane is the test solution, usually blood, whose pH is to be measured. It is the potential difference across the glass, between these two solutions, which is variable. The blood or other solution is separated from the calomel electrode by a porous plug and a potassium chloride salt bridge to minimise KCl diffusion. The potential difference across the system is about 60 mV per unit of pH change at 37◦C.
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Conference papers on the topic "CHLORINE 37"

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Ohara, Junichi, Shigeru Koyama, and Ken Kuwahara. "Falling Film Evaporation of Pure Refrigerant HCFC123 in a Vertical Rectangular Minichannel Consisting of Offset Strip Fins." In ASME 3rd International Conference on Microchannels and Minichannels. ASMEDC, 2005. http://dx.doi.org/10.1115/icmm2005-75128.

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In the present study, the characteristics of heat transfer and flow patterns are experimentally investigated on the falling film evaporation of pure refrigerant HCFC123 in a vertical rectangular minichannel consisting of offset strop fins. The refrigerant liquid is supplied to the channel through 37 holes of a distributor. The liquid flowing down vertically is heated electrically from the rear wall of the channel and evaporated. To observe the flow patterns during the evaporation process directly, a transparent vinyl chloride resin plate is placed as the front wall. The experimental parameters are as follows: the mass velocity G = 28∼70 kg/(m2s), the heat flux q = 20∼50 kW/m2 and the pressure P≈ 100 kPa. It is clarified that the heat transfer coefficient α depends on G and q in the region of vapor quality x ≥ 0.3 while there is little influence of G and q in the region x ≤ 0.3. From the direct observation using a high speed video camera and a digital still camera, flow patterns are classified into five typical ones: plane liquid film, wavy liquid film, liquid film accompanied with dry patch, liquid film accompanied with dripping and liquid film accompanied with mist. Then the relation between heat transfer and flow pattern is clarified. The results of heat transfer characteristics are also compared with some previous correlation equations.
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Saleem, Haleema, and Syed Javaid Zaidi. "Innovative Nanostructured Membranes for Reverse Osmosis Water Desalination." In Qatar University Annual Research Forum & Exhibition. Qatar University Press, 2020. http://dx.doi.org/10.29117/quarfe.2020.0023.

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Reverse osmosis (RO) is considered as the most widely utilized technique worldwide for water treatment. However, the commercial thin-film composite (TFC) membranes, which are normally made of polyamide (PA) through interfacial polymerization (IP), still experience certain major issues in performance and fabrication. The spin assisted layer-by-layer (SA-LbL) technique was established for overcoming some drawbacks with commercially available PA membranes. Also, recent investigations have recognized the nanoparticle inclusion into the selective layer as a powerful technique for improving the membrane efficiency. Hence, two different methodologies are presented here to improve the membrane performance, i.e., (1) SA-LbL technique to fabricate TFC membrane by the deposition of alternate ultrathin layers of different polyelectrolytes on polysulfone (PSF) commercial ultrafiltration membrane and (2) the nanoclay incorporation into the membranes during IP process to develop TFC membrane. Two types of nanoclays, cloisite (CS)-15A and montmorillonite (MNT), were incorporated to enhance the separation efficiency. This SA-LbL is an innovative method for the RO membrane manufacture, and has not been described earlier to the best of our knowledge. In addition, this work validated for the first time, the efficiency of the two nanoclays at the PA selective layer in the RO membrane. The membrane performance was evaluated using sodium chloride solution in a cross-flow permeation-testing cell for salt rejection and water flux. The results show significant improvement in water flux and salt rejection. The permeation test of 120 bilayers of poly (allylaminehydrochloride)/poly (vinylsulfate) on PSF substrate showed water flux of 37 L/ (m2.h) and salt rejection of 53%, for a 2000-ppm salt solution feed. The highest water flux of 40 L/m2.h with 80% salt rejection, relative to the control membrane was obtained for the membranes containing nanoclays at 25oC temperature, 40.0 bar pressure and 2000 ppm feed concentration. Thus, our study demonstrated that these TFC membranes are promising, and these novel fabrication techniques are great tool to manufacture the RO membrane.
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Taki, M., K. Sato, Y. Ikeda, M. Yamamoto, and K. Watanabe. "THE FUNCTIONAL DOMAIN OF PLATELET MEMBRANE GLYCOPROTEIN lb FOR VON WILLEBRAND FACTOR AND THROMBIN-BINDING." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643512.

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In this paper, we have examined the functional domain of platelet membrane glycoprotein lb (GPIb) by using elastase and a monoclonal antibody against GPIb which specific inhibits both von Willebrand factor (vWF) and thrombin interaction with platelets. Elastase was purified from human granulocytes by using affinity column chromatography according to the method of Okada et al.. A monoclonal antibody against platelet membrane GPIb (56-2) which inhibits both vWF and thrombin-binding to platelets was used for this study. Platelet surface glycoproteins were labelled with 3H by the method of Nurden et al.. Purified GPIb was obtained by a modification of the method of Coller et al. and labelled with 125I using chloramine-T method. Either 3H-labelled platelets or 125I-labelled GPIb was treated with elastase for various time periods. Elastase-treated l25I-GPIb was subjected to immunoaffinity chromatography using 56-2 antibody to determine the functional site of GPIb. Elastase inhibited platelet aggregation or 5-HT release by thrombin, ristocetin-induced platelet agglutination and vWF-binding to platelets in the presence of ristocetin in a dose- and time dependent manner. A fluorogram of SDS-PAGE of 3H-labelled platelets treated with elastase revealed that GPIb band was reduced gradually, and fragments with MW of 97, 70, 60, 47, 44, 37, 25 and 15 KD were released from the platelets. The 47 KD fragment was initially cleaved from the platelets, and subsequently other fragments were digested. Similar results were obtained when purified 125I-GPIb was digested by elastase. When the fragments from purified 125I-GPIb were reacted with 56-2 antibody, only three fragments with MW of 47, 44 and 25 KD were immunoisolated. The electrophoretic mobility of all these three bands was altered under reduced conditions, indicating that all these fragments contain disulfide bonds in their molecules. The 25 KD band showed a much fainter in 3H-labelling than in 125I-labelling.These results suggest that the functional domains of GPIb for both vWF and thrombin-binding may be located in a less glycosylated fragment with a MW of 25 KD on the distal portion of the GPIb molecule, which should contain at least one intramolecular disulfide bond.
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Reports on the topic "CHLORINE 37"

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Marchetti, A. A. Mass and charge distributions in chlorine-induced nuclear reactions. [[sup 35]Cl at E/A = 15 MeV, [sup 37]Cl at E/A = 7. 3 MeV]. Office of Scientific and Technical Information (OSTI), January 1991. http://dx.doi.org/10.2172/6804797.

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