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Relevant bibliographies by topics / Electrophorese en gel

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Academic literature on the topic 'Electrophorese en gel'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "Electrophorese en gel"

1

Lung-Escarmant, Brigitte, Carroline Mohammed, and Jean Dunez. "Nouvelles methodes de determination des Armillaires europeens: Immunologie et electrophorese en gel de polyacrylamide." Forest Pathology 15, no. 5-6 (1985): 278–88. http://dx.doi.org/10.1111/j.1439-0329.1985.tb01100.x.

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Tastet, Christophe, Michel Bossis, Jean-Pierre Gauthier, Lionel Renault, and Didier Mugniery. "Meloidogyne chitwoodi and M. fallax protein variation assessed by two-dimensional electrophoregram computed analysis." Nematology 1, no. 3 (1999): 301–14. http://dx.doi.org/10.1163/156854199508171.

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AbstractThe variation of total soluble protein extracts from white adult females of seven Meloidogyne chitwoodi and three M. fallax isolates were studied using two dimensional gel electrophoresis (2-DGE). The 2-D protein profiles were compared with a computed analysis system. A synthetic image or 'master' was constructed from proteinic spots present in each isolate. The comparison of the two species allowed detection of qualitative and, to a lesser extent, quantitative variations. Among the 243 proteinic spots present on the master, we have identified 75 monomorphic spots for both species and nine discriminative proteins for each of the two species. In addition, two isoelectric point variants and two quantitative variants were observed. The similarity index and the genetic distances between the ten isolates were calculated on the basis of homologous polymorphic spots. Dendrograms were constructed according to the UPGMA method. Significance of the results from the phenetic study was assessed by bootstrap analysis. The results from the clustering analysis allowed differentiation between both species and showed intraspecific variation among the M. chitwoodi isolates equal to that among the M. fallax isolates. Variabilite proteique de Meloidogyne chitwoodi et M. fallax etudiee par analyse informatisee d'electrophoregrammes bidimensionnels - La variabilite d'extraits proteiques solubles totaux de femelles blanches adultes de sept isolats de Meloidogyne chitwoodi et trois de M. fallax a ete etudiee par electrophorese sur gel en deux dimensions (2-DGE). Les profils proteiques bidimensionels ont ete compares grace a un systeme d'analyse informatise. Une image synthetique, ou image de reference, a ete construite a partir des spots proteiques toujours observes dans chaque isolat. La comparaison des deux especes a permis de detecter des variations qualitatives et, dans une moindre mesure, quantitatives. Parmi les 243 taches proteiques presentes sur l'image de reference, ont ete identifies 75 polypeptides communs aux deux especes et neuf proteines discriminantes pour chacune des deux especes. De plus, deux variants de point isoelectrique et deux variants quantitatifs ont ete observes. Les indices de similarite et les distances genetiques entre les dix isolats ont ete etudies a partir des taches polymorphes homologues. Les dendrogrammes ont ete construits selon la methode UPGMA. La signification des resultats phenetiques a ete estimee par une analyse "bootstrap". Les resultats de l'analyse en grappes ont permis de differencier les deux especes et ont revele une variabilite intraspecifique similaire entre isolats de M. chitwoodi et isolats de M. fallax.

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Morales-Romero, Gaspar, Paulina Fabiola Rodríguez-Flores, Aida Bejar-Ubaldo, et al. "Caracterización molecular de bacterias patógenas mediante electroforesis en gel de campos pulsados (PFGE)." Mexican Journal of Biotechnology 1, no. 2 (2016): 48–56. http://dx.doi.org/10.29267/mxjb.2016.1.2.48.

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La creciente necesidad de vigilancia de las enfermedades infecciosas re-emergentes hace necesario la aplicación de métodos moleculares de caracterización como la Electroforesis en Gel de Campos Pulsados-PFGE. En la primera colecta, el análisis de macrorrestricción de S. aureus revela una frecuencia media (0.54) del pulsotipo II, en comparación a la segunda colecta donde se observa una mayor heterogeneidad genética. S. enterica presentó algunos pulsotipos idénticos y otros pulsotipos presentaron una diversidad genética (ID=0.95), lo que nos sugiere, que no existe una relación epidemiológica con pulsotipos o serotipos particulares. Además, este estudio nos ayudara a crear nuestra base de datos de acuerdo a la PulseNet International del Centro de Control y Prevención de Enfermedades (CDC, USA)

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Tan, Timothy Ter Ming, Zong Ying Tan, Wei Liang Tan, and Peng Foo Peter Lee. "Gel electrophoresis." Biochemistry and Molecular Biology Education 35, no. 5 (2007): 342–49. http://dx.doi.org/10.1002/bmb.83.

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Grujić, Radoslav, Vesna Gojković Cvjetković, and Željka Marjanović-Balaban. "Separation of gliadins from wheat flour by capillary gel electrophoresis: optimal conditions." Foods and Raw Materials 8, no. 2 (2020): 411–21. http://dx.doi.org/10.21603/2308-4057-2020-2-411-421.

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Introduction. Gliadin proteins are one of the gluten fractions. They are soluble in alcoholic solution and divided into four groups (α + β, γ, ω1.2, and ω5-gliadins). In this paper gliadins were extracted from wheat flour, and optimal conditions for their separation were determined. Study objects and methods. The separation was performed by capillary gel electrophoresis on Agilent apparatus, CE 7100 (a capillary with an inner diameter of 50 μm, a total length of 33 cm, and an effective length of 23.50 cm). In order to determine the optimal conditions, different solvent concentrations (50, 60, and 70% ethanol), capillary temperatures (20, 25, 30, 35, and 40°C), and electrode voltages (–14.5, –16.5, –17.5 and –18.5 kV) were applied. Migration time and relative concentration of each protein molecules within gliadin fractions in the electrophoregram were analysed using Agilent ChemStation Software. Results and discussion. The optimal conditions for gliadin separation were: solvent 70% (v/v) ethanol, capillary temperature of 25°C, and electrode voltage of –16.5 kV. Under these conditions, the total proteins were indetified as Xav = 23.50, including α + β gliadin fraction (Xav = 7.50 and relative concentration RC = 28.29%), γ-gliadins (Xav = 5.00, RC = 26.66%), ω1.2-gliadins (Xav = 4.33, RC = 14.93%), and ω5-gliadins (Xav = 6.67, RC = 30.98%). Conclusion. The results of the research can be of fundamental importance in the study of gluten proteins and the influence of technological procedures on their change and the possibility of reducing the allergic effect of gluten during processing.

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Cunningham, Steven C., Brad McNear, Rebecca S. Pearlman, and Scott E. Kern. "Beverage-Agarose Gel Electrophoresis: An Inquiry-based Laboratory Exercise with Virtual Adaptation." CBE—Life Sciences Education 5, no. 3 (2006): 281–86. http://dx.doi.org/10.1187/cbe.06-01-0139.

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A wide range of literature and experience has shown that teaching methods that promote active learning, such as inquiry-based approaches, are more effective than those that rely on passive learning. Gel electrophoresis, one of the most common laboratory techniques in molecular biology, has a wide range of applications in the life sciences. As such, we chose it as a platform to expose high school and undergraduate students to the active process of scientific inquiry in general, while specifically teaching electrophoresis. First, we optimized DNA electrophoresis in the laboratory by using common beverages instead of standard media (e.g., Tris-based media). Second, we adapted this laboratory process of progressive optimization to a Web-based format in which students had to achieve all the same steps of optimization by performing serial electrophoreses. And third, we evaluated the use of this entirely Web-based virtual laboratory exercise in high school and undergraduate biology courses. Students learned fundamental and practical principles of electrophoresis, while experiencing the essential inquiry-based process of optimizing a technique, and they also enjoyed it. Our findings provide a readily accessible, inexpensive, and intriguing technique for teaching electrophoresis and the progressive optimization of a laboratory technique.

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Rotková, G. "Renaturation of telomere-binding proteins after the fractionation by SDS-polyacrylamide gel electrophoresis." Plant, Soil and Environment 53, No. 7 (2008): 317–20. http://dx.doi.org/10.17221/2211-pse.

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A simple method for identification and characterization of telomere-binding proteins is described in this article. After Sodium Dodecyl Sulphate-Polyacrylamide gel electrophoresis (SDS-PAGE), proteins are eluted, renatured and used for retardation analysis with labelled oligonucleotides corresponding to human and plant of telomeric sequences. We show here that this method is efficient to recover sequence-specific DNA-binding abilities of putative telomere-binding proteins.

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Grujić, Radoslav, Radoslav Grujić, Danica Savanović, and Danica Savanović. "Analysis of myofibrillar and sarcoplasmic proteins in pork meat by capillary gel electrophoresis." Foods and Raw Materials 6, no. 2 (2018): 421–28. http://dx.doi.org/10.21603/2308-4057-2018-2-421-428.

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Myofibrillar and sarcoplasmic proteins were extracted from pork meat (M. Longissimus dorsi) and then separated by capillary gel electrophoresis (CGE). Migration time and peak areas of individual protein molecules in the electropherogram were analysed. The electropherograms obtained after the separation of myofibrillar proteins contained  53 well-separated peaks, of which the following were identified: thymosin, myosin light chain-3 (MLC-3), myosin light chain-2 (MLC-2), troponin C, troponin I, myosin light chain-1 (MLC-1), tropomyosin 1, tropomyosin 2, troponin T, actin, desmin, troponin, C protein, and myosin heavy chain (MHC). The relative concentration of the identified myofibrillar proteins was 74.5%. Of the 56 separated sarcoplasmic proteins the following were identified: myoglobin, myokinase, triosephosphate isomerase, phosphoglycerate mutase, lactate dehydrogenase, glyceraldehyde phosphate dehydrogenase, aldolase, creatine kinase, enolase, phosphoglucose isomerase, pyruvate kinase, phosphoglucomutase, and phosphorylase b. The relative concentration of the identified sarcoplasmic proteins was 83.6% of all sarcoplasmic proteins extracted from the pork meat.

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Esser, K. A., M. O. Boluyt, and T. P. White. "Separation of cardiac myosin heavy chains by gradient SDS-PAGE." American Journal of Physiology-Heart and Circulatory Physiology 255, no. 3 (1988): H659—H663. http://dx.doi.org/10.1152/ajpheart.1988.255.3.h659.

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Separation of alpha- and beta-myosin heavy chains (MHCs) in cardiac ventricles of rats by gradient sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) was accomplished and compared with the separation of myosin isozymes obtained with pyrophosphate gels. Whole muscle homogenates were electrophoresed on a 4–9% linear gradient SDS polyacrylamide gel for 3–4 h. MHC bands were identified by the migration distance relative to a MHC standard and immunoblot results with a monoclonal antibody to MHC. The MHC bands were further identified as alpha and beta based on the electrophoretic mobility of ventricular homogenates from hypothyroid and hyperthyroid rats and ventricular and slow soleus skeletal muscle homogenates from control rats. The beta-MHC migrated faster than alpha-MHC, and laser densitometry revealed separate peaks when both MHCs were present. With homogenates containing MHC ranging from 0 to 100% alpha, the separation of MHCs with gradient SDS-PAGE correlated highly (r = 0.97) with separation of myosin isozymes by pyrophosphate gel electrophoresis. The SDS-PAGE technique reported herein is a quick, valid, and direct method for the identification and quantification of ventricular MHCs.

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Maddox, John. "Understanding gel electrophoresis." Nature 345, no. 6274 (1990): 381. http://dx.doi.org/10.1038/345381a0.

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Dissertations / Theses on the topic "Electrophorese en gel"

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Penel, Vincent. "L'électrophorèse en gel de polyacrylamide." Paris 5, 1988. http://www.theses.fr/1988PA05P254.

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VALTAT, BRUNO. "Etude electrophoretique du sperme humain coagule et liquefie : profils obtenus sur gel de polyacrylamide en tampon dissociant-discontinu." Strasbourg 1, 1990. http://www.theses.fr/1990STR15035.

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TUIL, ELISABETH. "Interet epidemiologique de l'etude des mobilites electrophoretiques en gel d'amidon des iosenzymes de 47 souches de staphylococcus aureus." Lyon 1, 1991. http://www.theses.fr/1991LYO1M404.

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4

Heinrich, Eric. "Utilisation d'une méthode électrophorétique en gel de polyacrylamide afin de mettre en évidence le passage trans-membranaire des endotoxines bactériennes au cours de l'hémodialyse." Strasbourg 1, 1992. http://www.theses.fr/1992STR10203.

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5

MAGNUSDOTTIR, SOFFIA. "Etude par spectroscopie et electrophorese capillaire de la migration d'adn en gel et en solution de polymeres." Paris 6, 1998. http://www.theses.fr/1998PA066220.

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Ce memoire presente une serie d'etudes experimentales destinees a ameliorer la comprehension des mecanismes moleculaires mis en jeu durant la separation electrophoretique de l'adn, et a utiliser cette comprehension pour ameliorer les performances de la technique. L'electrophorese de l'adn est un outil incontournable de tour projet en genetique, et est plus que jamais employee massivement dans le cadre des grands projets de sequencage du genome. Dans une premiere etude, on a employee le dichroisme lineaire (ld) pour suivre l'orientation d'adn double brin en cours d'electrophorese en gel d'agarose, afin d'identifier les modes de migration en fonction de la taille de l'adn et du champ electrique applique. Nous avons utilise les caracteristiques du profil de croissance ld a l'etablissement du champ, et de decroissance a l'arret du champ ; pour identifier les transitions entre ces modes de migration l'electrophorese capillaire en solutions de polymeres apparait de plus en plus comme l'alternative de choix aux separations en gel pour l'adn. Nous presentons une etude destinee a comprendre les facteurs responsables du developpement d'instabilites electrohydrodynamiques conduisant a l'agregation de l'adn, un probleme rencontre quand on chercher a separer des molecules de 20 kb et plus en electrophorese capillaire pulsee. Nous presentons egalement une nouvelle approche pour la collection d'adn par transfert direct sur une membrane en sortie de capillaire, ouvrant la possibilite d'utiliser l'electrophorese en mode micro-preparatif. La detection d'echantillons d'adn dans les gammes 150 bp-2 kbp et 120 kbp-23 kbp a ainsi ete effectuee par colorimetrie post-separation. Enfin, nous nous sommes interesses a l'autre limite de la gamme des tailles d'adn separables en capillaire, la resolution de petits fragments a la base pres. Nous avons utilise pour cela une nouvelle famille de milieux de separation, les polymeres associatifs. Nous avons demontre qu'une solution de polyoxyethylene de faible polydispersite, portant a ses extremites des blocs n-dodecane, constitue dans sa phase cubique un milieu de choix pour de telles separation.

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Mesbahi, Loubna. "Etude critique de la détermination automatisee du cholesterol des HDL, des VLDL et des LDL par électrophorèse en gel d'agarose." Bordeaux 2, 1993. http://www.theses.fr/1993BOR2P117.

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Cazeneuve, Cécile. "Caractérisation par électrophorèse en gradient de gel dénaturant des variations alléliques de deux polymorphismes de répétition en tandem situés dans une séquence consensus d'épissage de l'intron 8 du gène CFTR (Cystic fibrosis transmembrane conductance regulator)." Paris 5, 1995. http://www.theses.fr/1995PA05P051.

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DANCKAERT, PERRUCHOT ANNE. "Traitement informatique des autoradiographies de gels de sequences : conception et mise en oeuvre d'un systeme automatique d'interpretation d'autoradiographies, elaboration d'un algorithme de construction de la sequence consensus a partir de fragments." Paris 7, 1988. http://www.theses.fr/1988PA077045.

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YU, LONG XI. "Arns poly(a**(+)) cytoplasmiques specifiques de l'organogenese reproductrice a caractere sterile chez mercurialis annua l. (2n=16) : traduction in vitro-electrophorese bidimensionnelles, hybridations homologues et heterologues." Orléans, 1987. http://www.theses.fr/1987ORLE2050.

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Valmary, Laurence. "Phénotypes de résistance aux bêta-lactamines des souches de "Klebsiella" isolées dans un hôpital de long et moyen séjour : différenciation des souches résistantes par analyse du polymorphisme enzymatique." Paris 5, 1994. http://www.theses.fr/1994PA05P147.

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Books on the topic "Electrophorese en gel"

1

Dunn, M. J. Gel electrophoresis: Proteins. Bios Scientific Publishers in association with the Biochemical Society, 1993.

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Two-dimensional electrophoresis, and immunological techniques. Plenum Press, 1987.

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Dunn, Michael J. Gel electrophoresis: Proteins. Bios Scientific in association with the Biochemical Society, 1993.

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Dunn, Michael J. Gel electrophoresis: Proteins. BIOS Scientific Publishers in association with the Biochemical Society, 1993.

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Ohlendieck, Kay, ed. Difference Gel Electrophoresis. Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7268-5.

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Gel electrophoresis: Essential data. Wiley, 1994.

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Jones, P. Gel electrophoresis: Nucleic acids. Wiley, 1995.

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8

Cramer, Rainer, and Reiner Westermeier, eds. Difference Gel Electrophoresis (DIGE). Humana Press, 2012. http://dx.doi.org/10.1007/978-1-61779-573-2.

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Jordan, Kieran, and Marion Dalmasso, eds. Pulse Field Gel Electrophoresis. Springer New York, 2015. http://dx.doi.org/10.1007/978-1-4939-2599-5.

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Burmeister, Margit, and Levy Ulanovsky. Pulsed-Field Gel Electrophoresis. Humana Press, 1992. http://dx.doi.org/10.1385/0896032299.

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Book chapters on the topic "Electrophorese en gel"

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Manji, Husseini K., Jorge Quiroz, R. Andrew Chambers, et al. "Gel Electrophoresis." In Encyclopedia of Psychopharmacology. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_4272.

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Gooch, Jan W. "Gel Electrophoresis." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_13810.

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Peck, Stewart B., Carol C. Mapes, Netta Dorchin, et al. "Gel Electrophoresis." In Encyclopedia of Entomology. Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6359-6_1041.

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Engelhardt, Heinz, Wolfgang Beck, and Thomas Schmitt. "Capillary Gel Electrophoresis (CGE)." In Capillary Electrophoresis. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-85854-3_8.

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Stellwagen, Nancy C. "DNA Gel Electrophoresis." In Nucleic Acid Electrophoresis. Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-642-58924-9_1.

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Goubet, Florence, Paul Dupree, and Katja Salomon Johansen. "Carbohydrate Gel Electrophoresis." In Methods in Molecular Biology. Springer New York, 2020. http://dx.doi.org/10.1007/978-1-0716-0621-6_2.

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Mansour, Victoria J., and Jens R. Coorssen. "Quantitative Gel Electrophoresis." In Proteomics in Domestic Animals: from Farm to Systems Biology. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-69682-9_3.

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Goubet, Florence, Paul Dupree, and Katja Salomon Johansen. "Carbohydrate Gel Electrophoresis." In Methods in Molecular Biology. Humana Press, 2010. http://dx.doi.org/10.1007/978-1-61779-008-9_5.

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Frank, J. Howard, J. Howard Frank, Michael C. Thomas, et al. "Polyacridamide Gel Electrophoresis." In Encyclopedia of Entomology. Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6359-6_3034.

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Mesapogu, Sukumar, Chandra Mouleswararao Jillepalli, and Dilip K. Arora. "Agarose Gel Electrophoresis and Polyacrylamide Gel Electrophoresis: Methods and Principles." In Springer Protocols Handbooks. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-34410-7_5.

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Conference papers on the topic "Electrophorese en gel"

1

Akhter, Nazneen, A. R. Khan, Yusuf Talib, Shazia Shadab, and Ruhina Patel. "Analysis of Gel Electrophoresis Images." In 2008 First International Conference on Emerging Trends in Engineering and Technology. IEEE, 2008. http://dx.doi.org/10.1109/icetet.2008.132.

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Mayer, Pascal, Jean Sturm, and G. Weill. "DNA deformation in gel electrophoresis." In Laser Spectroscopy of Biomolecules: 4th International Conference on Laser Applications in Life Sciences, edited by Jouko E. Korppi-Tommola. SPIE, 1993. http://dx.doi.org/10.1117/12.146161.

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Lin, David C., Noshir A. Langrana, and Bernard Yurke. "The Migration of DNA Into a DNA-Crosslinked Gel Using Electrophoresis." In ASME 2003 International Mechanical Engineering Congress and Exposition. ASMEDC, 2003. http://dx.doi.org/10.1115/imece2003-43446.

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DNA-crosslinked polyacrylamide gels are polymeric electrolytes by virtue of the fact that DNA is negatively charged in an aqueous solution. As such, their mechanical properties can be altered by electrophoretic and electro-osmotic effects. Hybridization of single-stranded DNA with single-stranded sections of the crosslinks provides a novel means of altering gel mechanical properties. As a step toward exploring this means of altering gel mechanical properties, we report here on a study of the use of electrophoresis to introduce single stranded DNA into DNA crosslinked gels. Changes in elastic properties of the gel, before and after electrophoresis, were measured.

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"MATCHING TWO-DIMENSIONAL GEL ELECTROPHORESIS’ SPOTS." In International Conference on Bioinformatics Models, Methods and Algorithms. SciTePress - Science and and Technology Publications, 2012. http://dx.doi.org/10.5220/0003702401110117.

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Matsumoto, Mitsuhiro, and Masao Doi. "Dynamics of DNA in gel electrophoresis." In Slow dynamics in condensed matter. AIP, 1992. http://dx.doi.org/10.1063/1.42466.

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Kaya, Deniz Ece, Tanıl Kocagöz, Sesin Kocagöz, and Cengizhan Öztürk. "Observable Real-Time Pulsed-Field Gel Electrophoresis." In 2017 21st National Biomedical Engineering Meeting (BIYOMUT). IEEE, 2017. http://dx.doi.org/10.1109/biyomut.2017.8479196.

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Mese, Alev Kakac, Aykut Erdamar, and Ozlem Darcansoy Iseri. "Image analysis for single cell gel electrophoresis." In 2017 25th Signal Processing and Communications Applications Conference (SIU). IEEE, 2017. http://dx.doi.org/10.1109/siu.2017.7960416.

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Park, Sang Cheol, In Seop Na, Soo Hyung Kim, et al. "Lanes Detection in PCR Gel Electrophoresis Images." In 2011 IEEE 11th International Conference on Computer and Information Technology (CIT). IEEE, 2011. http://dx.doi.org/10.1109/cit.2011.89.

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Wang, Weixing. "Spot identification on 2D electrophoresis gel images." In Fourth International Conference on Photonics and Imaging in Biology and Medicine, edited by Kexin Xu, Qingming Luo, Da Xing, Alexander V. Priezzhev, and Valery V. Tuchin. SPIE, 2006. http://dx.doi.org/10.1117/12.710884.

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de Carmejane, Olivia, Jeffrey J. Schwinefus, and Michael D. Morris. "Plasmid topoisomer separation by capillary gel electrophoresis." In BiOS '99 International Biomedical Optics Symposium, edited by Joseph R. Lakowicz, Steven A. Soper, and Richard B. Thompson. SPIE, 1999. http://dx.doi.org/10.1117/12.347533.

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Reports on the topic "Electrophorese en gel"

1

Uberbacher, E. C., and G. J. Bunick. Purification of nucleoprotein particles by elution preparative gel electrophoresis. Office of Scientific and Technical Information (OSTI), 1986. http://dx.doi.org/10.2172/5127796.

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R. JOHNSTON. THERMAL DETECTION OF DNA AND PROTEINS DURING GEL ELECTROPHORESIS. Office of Scientific and Technical Information (OSTI), 2000. http://dx.doi.org/10.2172/768736.

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Xu, Aoshuang. Development in electrophoresis: instrumentation for two-dimensional gel electrophoresis of protein separation and application of capillary electrophoresis in micro-bioanalysis. Office of Scientific and Technical Information (OSTI), 2008. http://dx.doi.org/10.2172/1342558.

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Dunn, Bruce E., Martin J. Blaser, and Edward L. Snyder. Two-Dimensional Gel Electrophoresis and Immunoblotting of Campylobacter Outer Membrane Proteins. Defense Technical Information Center, 1987. http://dx.doi.org/10.21236/ada265461.

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Gaul, Stephen B., Stephanie Wedel, Matthew M. Erdman, et al. Identification of Swine Salmonella serotypes Using Pulsed-field Gel Electrophoresis of Conserved Xba1 Fragments. Iowa State University, 2007. http://dx.doi.org/10.31274/ans_air-180814-809.

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Yinfa, Ma. Indirect fluorometric detection techniques on thin layer chromatography and effect of ultrasound on gel electrophoresis. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/6045672.

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Little, Stephen F. Western Blot Analysis of the Exotoxin Components From Bacillus anthracis Separated by Isoelectric Focusing Gel Electrophoresis. Defense Technical Information Center, 2004. http://dx.doi.org/10.21236/ada435242.

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McGregor, David A. Optimization of separation and detection schemes for DNA with pulsed field slab gel and capillary electrophoresis. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/10116369.

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