Relevant bibliographies by topics / Antigen antibody reaction

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

Academic literature on the topic 'Antigen antibody reaction'

Author: Grafiati
Published: 4 June 2021
Last updated: 8 February 2022

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Journal articles on the topic "Antigen antibody reaction"

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Montero, Claudio. "The Antigen-Antibody Reaction in Immunohistochemistry." Journal of Histochemistry & Cytochemistry 51, no. 1 (January 2003): 1–4. http://dx.doi.org/10.1177/002215540305100101.

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The problems of major concern in immunohistochemical practice are discussed in the following order: (a) the mechanism of the Ag-Ab reaction in fixed tissue as opposed to the in vitro reaction; (b) the chemistry of fixation and its influence on the final result of the immunohistochemical reaction; (c) the various procedures used for antigen retrieval in formaldehyde-fixed tissue; and (d) the consideration of the possible mechanism underlying heat-induced antigen retrieval. Suggestions for further work to attempt a clarification of the mechanism involved in the Ag-Ab reaction in immunohistochemistry resorting to existing histochemical methods for the demonstration of protein side groups are presented, together with some examples already published.
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Kobayashi, T., I. Yokoyama, H. Ogawa, T. Nagasaka, D. Liu, T. Kato, T. Tokoro, et al. "Suppression of antigen-antibody reaction in xenotransplantation." Transplantation Proceedings 32, no. 2 (March 2000): 287–88. http://dx.doi.org/10.1016/s0041-1345(99)00959-8.

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Chernykh, Oleg Yu, Elmira A. Yanikova, Mikail M. Mikailov, Akhmed A. Khalikov, and Atiya T. Gulieva. "Indirect hemagglutination reaction in ram infectious epididymitis for indication of Brucella ovis antigen in biomaterial." Veterinaria Kubani, no. 5 (October 30, 2020): 23–25. http://dx.doi.org/10.33861/2071-8020-2020-5-23-25.

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The reaction of indirect hemagglutination with an antibody erythrocyte diagnosticum is one of the promising methods for identifying the causative agent of infectious diseases or antigen. This preparation has not yet been developed for the diagnosis of infectious epididymitis of rams. The results of the preparation of an antibody erythrocyte diagnosticum in the reaction of indirect hemagglutination for the detection of the causative agent of infectious epididymitis in various biological material are presented in the article. As a result of scientific research, authors developed the method for obtaining an original Brucella ovis antibody diagnosticum for the reaction of indirect hemagglutination by sensitizing sheep erythrocytes with hyperimmune Brucella ovis serum using alizarin blue indicator of the epididymitic pathogen or antigen in biomaterial as the conjugate. Studies have shown the specificity and higher sensitivity of the indirect hemagglutination reaction with the antibody erythrocyte diagnosticum, compared with the antibody neutralization reaction and the bacteriological method, and its suitability for the indication of Brucella ovis antigen in biomaterial and environmental objects. It was also found that the reaction of indirect hemagglutination with antibody diagnosticum is much faster than the reaction of neutralization of antibodies and the bacteriological method. Research to improve the diagnosis of infectious ram epididymitis caused by Brucella ovis has been completed with the development of the antibody erythrocyte diagnosticum for the indirect hemagglutination reaction.The high specificity and activity of this preparationwas established by the authors. As a result of the studies carried out to test the diagnostic value of the antibody diagnosticum, a higher sensitivity of the indirect hemagglutination reaction using the new antibody diagnosticum, compared with the neutralization reaction of antibodies and the bacteriological method, and the suitability of using the diagnosticum for the indication of the Brucella ovis antigen in biomaterial, was established, which meets the requirements for express methods for detecting antigens in pathological material.
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Grushevskaja, G. V., and A. I. Khmelnitsky. "Sequence of bifurcations in an ‘antigen-antibody’ reaction." Journal of Molecular Recognition 9, no. 5-6 (October 1996): 570–74. http://dx.doi.org/10.1002/(sici)1099-1352(199634/12)9:5/6<570::aid-jmr304>3.0.co;2-k.

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MALMBORG, A. C., A. MICHAELSSON, M. OHLIN, B. JANSSON, and C. A. K. BORREBAECK. "Real Time Analysis of Antibody-Antigen Reaction Kinetics." Scandinavian Journal of Immunology 35, no. 6 (June 1992): 643–50. http://dx.doi.org/10.1111/j.1365-3083.1992.tb02970.x.

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Allan, J. C., and P. S. Craig. "Partial characterization and time course analysis of Hymenolepis diminuta coproantigens." Journal of Helminthology 68, no. 2 (June 1994): 97–103. http://dx.doi.org/10.1017/s0022149x00013596.

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AbstractAn analysis of Hymenolepis diminuta specific antigens in infected rat faeces was carried out. Using a capture type antibody sandwich ELISA assay based on a hyperimmune rabbit anti-worm somatic antisera it was demonstrated that, although antigen was present in faeces before patency, the onset of egg production led to a sharp increase in the levels of parasite antigen in the faeces. Levels of antigen in host faeces were independent of worm burden. Parasite eggs did not contribute significantly to faecal antigen levels. Western blot analysis indicated a number of highly specific antigens at around Mr 69,000, Mr 37,000, Mr 50,000 and Mr 27,000 with a low molecular weight smear at between Mr 30,000 and Mr 34,000 present in the faeces of H. diminuta infected rats. Some cross reaction occurred with an antigen of around Mr 66,000 in the faeces of non H. diminuta infected rodents. Antibody activity against this antigen was removed by affinity adsorption of the antibody solution against normal rat faeces.
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Wajer, S. D., and H. K. Charles. "A SEM analysis of thin indium films for immunoassay applications." Proceedings, annual meeting, Electron Microscopy Society of America 45 (August 1987): 938–39. http://dx.doi.org/10.1017/s0424820100128973.

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Indium metal films have been used as host substrate materials for biological immunoassays. Indium film immunoassays involve the optical detection of specific antibody-antigen reactions using either transmitted or reflected white light. In the immunoassay process, drops of a purified antibody solution are placed on 5 to 25 nm thick indium films supported on a glass substrate (i.e., indium slide). After incubation, the antibody solution is washed off, leaving visible spots of reactive antibody. The slide is then coated with an unrelated protein which covers any non-antibody areas thus making the whole slide appear optically uniform. Placing the indium slide in an appropriate antigen solution will cause a visible response, since the antibody-antigen reaction complex will contain two layers of protein and will be darker than the surrounding background. In addition to the biological reaction sensitivities, the indium film immunoassay response is critically dependent on the bulk and surface properties of the indium film.
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Hohsaka, Takahiro, Kazuo Kawashima, and Masahiko Sisido. "Photoswitching of NAD+-mediated enzyme reaction through photoreversible antigen-antibody reaction." Journal of the American Chemical Society 116, no. 1 (January 1994): 413–14. http://dx.doi.org/10.1021/ja00080a064.

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YANAGI, AKIRA, and HIROAKI YAMAMOTO. "Monoclonal antibody against a conjugation-specific nuclear antigen in Paramecium caudatum." Journal of Cell Science 95, no. 2 (February 1, 1990): 287–91. http://dx.doi.org/10.1242/jcs.95.2.287.

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To understand molecular mechanisms controlling the sexual reproduction process (conjugation) in Paramecium caudatum, we have tried to detect conjugation-specific antigens with monoclonal antibodies. We obtained a monoclonal antibody (CSN-1) against an antigen that appears in the nuclei only during conjugation. This nuclear antigen began to appear both in micro- and macronuclei at micronuclear stage II or III early in the conjugation process (4 h after the mating reaction at 25°C). In the macronucleus, the nuclear antigen persisted until the stage of macronuclear fragmentation (about 35 h) and then disappeared before degeneration of the macronuclear fragments. In the micronucleus, the antigen existed until the crescent stage (stage V) of the first meiotic division (8h). The antigen in the micronucleus disappeared after the crescent stage but reappeared again in the eight nuclei produced by the third postzygotic division (25 h). Then it persisted only in the four macronuclear anlagen differentiated from the eight nuclei (about 30 h). When exconjugant cells had undergone two successive postconjugational cell divisions and thus possessed only one new macronucleus as in the vegetative cells, the antigen disappeared completely from the new macronucleus in most cells. These cells without the antigen began to appear about 50 h after the mating reaction. As the antigen is specific to conjugation and localized in nuclei, it may play some important role(s) in the conjugation process.
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Sudjana, Dina, Lia Amalia, and Saepul Adnan. "Preliminary Immunochemical Studies to Detect Lard." Indonesian Journal of Halal Research 2, no. 1 (March 1, 2020): 8–12. http://dx.doi.org/10.15575/ijhar.v2i1.7819.

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Detection of lard in food using immunochemical methods has been carried out. This method has been applied and developed in food analysis. The purpose of this study was to detect the presence of lard in food. The method used was immunochemical which in this case is tested to its application in food analysis. The principle method is based on the antigen-antibody reaction, between lipids as antigens that can be deposited by antibodies in the agar medium. Antibodies were obtained by inducing lard into the blood vessels of rabbits. This method is based on the antigen-antibody reaction between fat as an antigen and antibodies that contain anti-lard as reagents and the occurrence of precipitation in agar media. The antibody was obtained by inducing lard, pork broth, and pig plasma into the blood vessels of rabbits. The results of this study were significant.
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Dissertations / Theses on the topic "Antigen antibody reaction"

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Andersson, Kerstin. "Antigen-antibody reactions a study of functional structures and non-immunological interactions /." Lund : Dept. of Biochemistry, Lund University, 1995. http://catalog.hathitrust.org/api/volumes/oclc/39264530.html.

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Schuman, Jason Tyler. "Structural and dynamical investigations of the interaction between the MUC1 tumor antigen and the humoral immune system : towards the design of a second generation cancer vaccine /." Thesis, Connect to this title online; UW restricted, 2003. http://hdl.handle.net/1773/8613.

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Thornton, Gail Marilyn. "Biolithography : selective joining using antibody-antigen reactions." Thesis, Massachusetts Institute of Technology, 1995. http://hdl.handle.net/1721.1/42816.

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Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Mechanical Engineering, 1995.
Includes bibliographical references (p. 211-212).
Biolithography is a contribution to the field of Solid Free Form Fabrication. Part production is based on selective joining using antibody- antigen reactions, where the selectively is based on the thermal sensitivity of such proteins. Antibodies and antigens can be chemically immobilized to a variety of substrate materials: polymeric, ceramic and metallic. In the present investigation, antibody coated 1 [mu]m polystyrene beads and antigen coated glass surface substrates, as well as, antigen solutions were used. Both antibodies and antigens were multivalent i.e. have more that one binding site for each other; thus, two antibody coated beads could be held together by one antigen. Selective deposition was demonstrated by thermally deactivating antigen coated onto glass and precipitating antibody coated beads. Bead deposition was selective to the regions of remaining active antigens; thus, revealing the defined deactivated region. Thermal deactivation of the antigen coated substrate was first demonstrated with a 90°C water jet and improved using an argon ion laser which produced line widths on the order of tens of microns. Selective definition of geometry was an extension of the coating process precipitating not one but two bead layers and linking beads using antigen in solution. The thermal deactivation mechanism was a modified 90°C water jet that had line width resolution on the order of millimeters. Line definition was on both antigen coated bases and bound bead bases; thus, thermal deactivation was effective on both immobilized antigen (glass) and antibody (bead). The selective deposition of antibody coated substrate was demonstrated by thermally deactivating immobilized antigens and antibodies on surface substrates. Definition resolution was dependent on the thermal deactivation mechanism used.
by Gail Marilyn Thornton.
S.M.
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Tsui, Ka-kit, and 徐家傑. "Seasonal variation of serum prostate-specific antigen levels in Hong Kong." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2008. http://hub.hku.hk/bib/B40738292.

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Tsui, Ka-kit. "Seasonal variation of serum prostate-specific antigen levels in Hong Kong." Click to view the E-thesis via HKUTO, 2008. http://sunzi.lib.hku.hk/hkuto/record/B40738292.

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Otali, Dennis. "The combined effect of formalin fixation and individual steps in tissue processing on immunorecognition." Birmingham, Ala. : University of Alabama at Birmingham, 2007. https://www.mhsl.uab.edu/dt/2008r/otali.pdf.

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Gonzalez, Elfwing Olivia, and Elin Nilsson. "Utvärdering av icke-invasiva metoder för diagnostik av Helicobacter pylori-infektion : En systematisk litteraturstudie." Thesis, Hälsohögskolan, Jönköping University, HHJ, Avd. för naturvetenskap och biomedicin, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-48758.

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Helicobacter pylori-infektion är en av de ledande orsakerna till utvecklingen av maligniteter i ventrikeln. Tillämpning av pålitliga analytiska metoder är därför väsentlig för en korrekt diagnostik och behandling av infektionen. Syftet med studien var att ge en översikt av icke-invasiva metoder som tillämpas för påvisning av H. pylori och utvärdera vilken metod som är bäst lämpad, med avseende på metodens prestandaegenskaper och det kliniska tillståndet hos patienten. En systematisk litteraturöversikt utfördes, genom sökning efter vetenskapliga artiklar med inklusions- och exklusionskriterier i databaserna PubMed och CINAHL. Utvalda artiklar kvalitetsgranskades och 20 studier inkluderades i resultatet. Sammanställt hade fecesantigentester en sensitivitet och specificitet på 92,64% respektive 91,47%, antikroppstester hade 97,20% respektive 81,59%, urea utandningstester hade 91,40% respektive 91,70% och polymeraskedjereaktionen hade 75,45% respektive 98,30%. Därutöver hade kliniska tillstånd såsom atrofisk gastrit, intestinal metaplasi och gastrointestinal blödning en negativ påverkan på metodernas diagnostiska tillförlitlighet. Studien konstaterade att beträffande metodens prestanda är fecesantigentester mest lämpliga för påvisning av H. pylori- infektion. Vid allvarligare kliniska åkommor bör minst två icke-invasiva diagnostiska metoder tillämpas för att säkerställa pålitliga resultat.
Helicobacter pylori infection is one of the leading causes of ventricular pathologies. Reliable analytic methods are therefore crucial for the correct diagnosis and treatment of the infection. The aim of this study was to provide an overview of non-invasive diagnostic methods used for the detection of H. pylori and to evaluate which method is most suitable, considering its performance and the clinical condition of the patient. A systematic literature review was conducted, searching peer-reviewed research articles with inclusion and exclusion criteria on the databases PubMed and CINAHL. An assessment of the selected articles quality resulted in the inclusion of 20 articles. Overall, stool antigen tests had a sensitivity and specificity of 92,64% and 91,47% respectively, antibody tests 97,20% and 81,59% respectively, urea breath tests 91,40% and 91,70% respectively, and the polymerase chain reaction 75,45% and 98,30% respectively. Furthermore, conditions such as atrophic gastritis, intestinal metaplasia and gastrointestinal bleeding had a negative impact on the diagnostic accuracy of the methods. This study concluded that, regarding the methods performance, stool antigen tests are more suitable for detecting a H. pylori infection. With the mentioned clinical conditions, at least two non- invasive diagnostic methods should be used to ensure reliable results.
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De, Leon Ellen Jane Biotechnology &amp Biomolecular Sciences Faculty of Science UNSW. "Engineering antibodies against complex platelet antigens using phage display technology." Awarded by:University of New South Wales, 2007. http://handle.unsw.edu.au/1959.4/37009.

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Platelets are small anucleate cell fragments found in blood whose physiological role is important in maintaining haemostasis. In vivo, platelet surface glycoproteins mediate the mechanistic roles of platelets, and polymorphic changes to these glycoproteins have been observed to have significant effects on the platelet cellular function and such changes may include over-expression, under-expression and antigenicity of the protein. Human platelet antigens (HPA) are a result of polymorphic differences in platelet surface glycoproteins which have been found to be variably expressed in the population. Foetal maternal alloimmune thrombocytopaenia (FMAIT) is a condition that is observed in the unborn foetus and neonates due to HPA incompatibility between the mother and the foetus. HPA incompatibility accounts for a majority of severe thrombocytopaenic cases in neonates, and delayed diagnosis and treatment of such a condition often lead to intracranial haemorrhage. The risk in neonates diagnosed with FMAIT becomes increasingly significant in cases where intra-uterine (during pregnancy) platelet transfusion is the only effective therapeutic option. There are currently no antenatal screening programs for this condition, and laboratory diagnosis of FMAIT relies on the detection of maternal alloantibodies and parental HPA typing. For these reasons a significant amount of research is currently being invested into the isolation of recombinant antibodies with specific reactivity against FMAIT-related platelet antigens. Stable and specific recombinant platelet antibodies have great potential as a diagnostic agent in antenatal screening and broad-scale HPA typing of blood donors for platelet transfusion. Further characterisation of the isolated antibody may lead to a possible therapeutic agent. Studies by previous researchers have shown that the traditional methods (ie. Mouse monoclonal and EBV transformation) of obtaining monoclonal antibodies against FMAIT-related antigens have proven unsuccessful. The continuing progress in the discipline of phage display has produced several novel antibodies against self and non-self antigens. A further advantage in the application of phage display technology for the isolation of novel antibodies is the easy transition from bacterial to mammalian expression for the characterisation of glycosylated antibodies. The main focus of this project was to create and isolate a recombinant human anti-HPA-3a antibody using phage display for its possible application as a therapeutic or diagnostic agent.
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Mummert, Mark E. "Stability in antigenic reactivity of the major outer surface protein, OspA, in borrelia burgdorferi, during persistent infection in Syrian hamsters." Virtual Press, 1992. http://liblink.bsu.edu/uhtbin/catkey/845968.

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The spirochete Borrelia burgdorferi is the causative agent of Lyme disease, a multisystem disorder that can cause a variety of disorders in susceptible mammalian hosts. The immune response of infected mammals, including humans, is ineffective in clearing B. burgdorferi as demonstrated by the ability to reisolate the spirochete from naturally and experimentally infected hosts after extended periods of time. Recent evidence suggests that this pathogen evades the immune response in part through changes in antigenic reactivity.The purpose of this study was to determine if outer surface protein A (OspA) of B. burqdorferi varies in the course of infection in Syrian hamsters and thus potentially plays a role in evading the host immune response. To assess the degree of change, differences in the binding of a murine monoclonal antibody (H5332) were measured using IFA and ELISA techniques over a 9-week period of time.Results of this study suggest that OspA is persistently expressed in infected Syrian hamsters for at least 9-weeks. Moreover, this protein, or at least the epitope that H5332 binds with, is stably expressed. These results indicate OspA, or at least the epitope of OspA that I probed, does not appear to contribute to the evasive mechanisms of 8. burgdorferi in Syrian hamsters.
Department of Biology
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Luo, Cheng-Ping. "Detection of antibody antigen reactions using surface acoustic wave and electrochemical immunosensors." [S.l.] : [s.n.], 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=971863121.

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Books on the topic "Antigen antibody reaction"

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An introduction to immunohematology. 3rd ed. Philadelphia: W.B. Saunders Co., 1994.

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Padlan, Eduardo. Antibody-antigen complexes. Austin: R.G. Landes, 1994.

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Mayer, Gaetan. Amplification methods for the immunolocalization of rare molecules in cells and tissues. Jena, Germany: Urban & Fischer, 2001.

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I͡U︡, Polevai͡a︡ O., and Piruzi͡a︡n L. A. 1937-, eds. Biokhimicheskie osnovy immuniteta k nizkomolekuli͡a︡rnym khimicheskim soedinenii͡a︡m. Mosvka: "Nauka", 1985.

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Shammala, Wesam Abu. Human plasma Kallikrein and pre-Kallikrein: Immunochemical adsorption studies using selected non-biological surfaces. Dublin: University College Dublin, 1999.

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Dember, Laura M. Human immunodeficiency virus antibodies and antigen in infants born to seropopositive mothers. [New Haven: s.n.], 1988.

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Wendt, Hans. Leucine zipper peptides as models for protein folding. Konstanz: Hartung-Gorre, 1995.

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Rosdolsky, Maria. Application of monoclonal antibodies in clinical oncology. Bethesda, MD: U.S. DHHS, PHS, NIH, National Cancer Institute, International Cancer Research Data Bank, 1990.

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Monoclonal antibody to the immunodominant lipopolysaccharide antigen of bacteroides fragilis cross-reacting with type II group B streptococci. Turku: Turun yliopisto, 1988.

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Autophagy in infection and immunity. Dordrecht: Springer, 2009.

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Book chapters on the topic "Antigen antibody reaction"

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Paraf, A., and G. Peltre. "Antigen-antibody reaction." In Immunoassays in Food and Agriculture, 32–35. Dordrecht: Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-3822-2_5.

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Jefferis, Roy, and Ian Deverill. "The antigen antibody reaction." In Principles and Practice of Immunoassay, 1–18. London: Palgrave Macmillan UK, 1991. http://dx.doi.org/10.1007/978-1-349-11234-0_1.

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Verma, Parag, Ankur Dumka, Alaknanda Ashok, Amit Dumka, and Anuj Bhardwaj. "Antigen–Antibody Reaction-Based Immunodiagnostics Method." In Covid-19, 165–200. Boca Raton: CRC Press, 2021. http://dx.doi.org/10.1201/9781003131410-4.

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Alexander, Peter W. "Antibody-Antigen Precipitin Reaction Monitoring with an Ion Selective Electrode." In Electrochemical Sensors in Immunological Analysis, 195–202. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4899-1974-8_14.

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Liu, Yu-Ting, and Shinya Toyokuni. "Intermittent Microwave Irradiation Facilitates Antigen-Antibody Reaction in Western Blot Analysis." In Methods in Molecular Biology, 307–12. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-59745-542-8_33.

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Rebelo, Magda, Teresa Diogo, and Sean McKee. "Modelling a Competitive Antibody/Antigen Chemical Reaction that Occurs in the Fluorescence Capillary-Fill Device." In Mathematics in Industry, 229–36. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-05365-3_31.

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Deshpande, S. S. "Antigen-Antibody Reactions." In Enzyme Immunoassays, 52–71. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-1169-0_3.

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Virella, Gabriel. "Antigen-antibody reactions." In Medical Immunology, 83–92. 7th edition. | Boca Raton : Taylor & Francis, 2020.: CRC Press, 2019. http://dx.doi.org/10.1201/9780429278990-8.

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Mutharia, Lucy M., and Joseph S. Lam. "Antigen-Antibody Reactions." In Methods for General and Molecular Microbiology, 138–67. Washington, DC, USA: ASM Press, 2014. http://dx.doi.org/10.1128/9781555817497.ch8.

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Tsuji, M., and D. J. Reen. "Influence of altered ELISA antigen-antibody reaction kinetics on measuremennt of IgA2 subclass levels in biological fluids." In Advances in Mucosal Immunology, 904–5. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-1848-1_289.

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Conference papers on the topic "Antigen antibody reaction"

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Joseph, David. "Antigen-antibody reaction studied by laser light scattering." In 2008 International Conference on Advanced Optoelectronics and Lasers (CAOL). IEEE, 2008. http://dx.doi.org/10.1109/caol.2008.4671893.

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Lin, Jung-Yi, Da-Jen Yao, and Fangang Tseng. "Functional antibody-antigen reaction on the surface of iron oxide nanoparticles." In 2006 1st IEEE International Conference on Nano/Micro Engineered and Molecular Systems. IEEE, 2006. http://dx.doi.org/10.1109/nems.2006.334714.

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David, P. J., and Deep N. Tripathi. "Cluster formation of antigen antibody reaction studied by laser light scattering." In BiOS Europe '95, edited by Britton Chance, David T. Delpy, and Gerhard J. Mueller. SPIE, 1995. http://dx.doi.org/10.1117/12.228666.

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Yamatogi, S., M. Fukuyama, H. Ding, M. Nishida, C. Kawamoto, Y. Amemiya, T. Ikeda, et al. "Selective Detection of Antigen-Antibody Reaction using Si Ring Optical Resonators." In 2009 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2009. http://dx.doi.org/10.7567/ssdm.2009.j-8-2.

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Nishida, M., M. Fukuyama, Y. Abe, Y. Amemiya, T. Ikeda, A. Kuroda, and S. Yokoyama. "Detection of Antigen-Antibody Reaction Using Si Ring Optical Resonators Functionalized with an Immobilized Antibody-Binding Protein." In 2010 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2010. http://dx.doi.org/10.7567/ssdm.2010.p-11-1.

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Endo, Tatsuro, Kenji Sueyoshi, and Hideaki Hisamoto. "Nanoimprinted two-dimensional photonic crystal for detection of fibrinogen using antigen-antibody reaction." In 2015 20th Microoptics Conference (MOC). IEEE, 2015. http://dx.doi.org/10.1109/moc.2015.7416439.

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Okamoto, Shogo, Yusuhide Ohno, Kenzo Maehashi, Koichi Inoue, and Kazuhiko Matsumoto. "6.1.3 Fragment-Modified Graphene FET for Highly Sensitive Detection of Antigen-Antibody Reaction." In 14th International Meeting on Chemical Sensors - IMCS 2012. AMA Service GmbH, Von-Münchhausen-Str. 49, 31515 Wunstorf, Germany, 2012. http://dx.doi.org/10.5162/imcs2012/6.1.3.

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Nakahara, Takuya, Ryo Oe, Taira Kajisa, Shuji Taue, Takeo Minamikawa, and Takeshi Yasui. "Application of Refractive-index-sensing Optical Frequency Comb for Biosensing of Antigen-antibody Reaction." In CLEO: Science and Innovations. Washington, D.C.: OSA, 2021. http://dx.doi.org/10.1364/cleo_si.2021.stu2a.2.

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Kieffer, N., L. Edelman, P. Edelman, C. Legrand, J. Breton-Gori us, and W. Vainchenker. "A MONOCLONAL ANTIBODY AGAINST AN ERYTHROID ONTOGENIC ANTIGEN IDENTIFIES GP IV ON HUMAN PLATELETS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643532.

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Abstract:
A murine monoclonal antibody (FA6-152), obtained by immunizing mice with fetal human erythrocytes agglutinated fetal but not adult erythrocytes and bound to both adultand fetal monocytes, platelets andreticulocytes. The antibody did not react with lymphocytes or granulocytes (P. Edelman et al., Blood, 1986, 67, 56). Fluorescent labeling of marrow cells and of in vitro BFU-E, CFU-GM and CFU-MK derivedcolonies revealed that the antigen defined by FA6 was absent from the granulocytic precursors and was detected on the megakaryo-cytic lineage at a later stage of differentiation than major platelet membraneglycoprotein markers. In contrast,the antigen appeared as a very early marker of erythroid differentiation.In the present report, we performed immunoprecipitation experiments on surface labeled platelets toidentify the platelet FA6 antigen.A band of apparent Mr - 85,000 wasimmunoprecipitated from iodinated platelets. This band was also revealed after periodate/Na[3H]BH4 orneuraminidase galactose oxidase/Na[3H]BH4 surface labeling of the platelets, providing evidence that the FA6 antigen corresponds to platelet GP IV. Preliminary studies revealed that FA6-IgG inhibited platelet aggregation induced by low doses of thrombin without affecting the platelet release reaction. Our results therefore suggest that GP IV, which isa multi-lineage hematopoietic differentiation marker, could play a role in cell-cell or cell-substrateinteractions common to different hematopoietic cell types.
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Gunda, Naga Siva Kumar, and Sushanta K. Mitra. "Microfluidic Based Biosensor for Detection of Cardiac Markers." In ASME 2013 Fluids Engineering Division Summer Meeting. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/fedsm2013-16270.

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Myocardial Infarction (MI) occurs when the blood flow to the heart is blocked. It is major threat to human kind. Current laboratory and ELISA tests are expensive, time consuming, and are not very sensitive. Biosensors can play an important role in the diagnosis of MI without relying on hospital visits. Therefore, researchers are focusing to develop rapid, hand-held, inexpensive biosensors for detecting cardiac markers. In the present study, one of the cardiac markers (Troponin T) is detected using microfluidic based biosensor. Troponin T (cTnT) releases in to the blood serum within 4–6 h after minor heart attack and remains elevated for up to 2 weeks, which will help in diagnosing the heart condition. In this work, a microfluidic channel with an array of gold strips is considered for detecting and quantifying the Troponin T in an aqueous solution. Troponin T primary (capture) antibody is immobilized on gold strip using self assembled monolayer (SAM) consisting of a homogeneous mixture of oligo (ethylene glycol) (OEG)-terminated alkanethiolate and mercaptohexadecanoic acid (MHDA). Then, an aqueous solution containing Troponin T antigen is injected into the microchannel to facilitate antibody-antigen reaction to take place in less time. Later, FITC tagged Troponin T secondary (detection) antibody is dispensed in to the channel for quantification of Troponin T antigen. Using confocal fluorescent reader, the variation of fluorescent intensity across the microchannel is measured and quantified the concentration of Troponin T antigen with calibrated samples. Contact angle measurement system, Fourier Transform Infrared Spectroscopy and Ellipsometer are used to characterize the surface properties at each stage of biomolecule immobilization.
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