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Keybot 130 Results  www.usc.es
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6. Patterns of human diversity of mitochondrial DNA
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6. Patrones de diversidad humana de marcadores del ADN mitocondrial
  Collaborations | QBFE  
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We are collaborating with the Supramolecular and Biological Chemistry group at the University of Santiago de Compostela (Prof. Dr. José L. Mascareñas and Prof. Dr. Juan R. Granja) to identify and control supramolecular interactions in DNA, peptide nanotubes and other species, employing spectroscopic techniques.
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Venimos colaborando con el grupo de Química Biológica y Supramolecular de la Universidad de Santiago de Compostela (Prof. José L. Mascareñas y Prof. Juan R. Granja) para identificar y controlar interacciones supramoleculares en ADN, nanotubos peptídicos y otras especies, mediante técnicas espectroscópicas.
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-The genetic material: DNA and RNA, analysis and structure. Genome. Chromatine and chromosomes. Karyotype.
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-La herencia del sexo. Herencia de rasgos determinados por genes localizados en los cromosomas sexuales.
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- Transmisión do material hereditario. Principio da segregación. Dominancia. Epistase.
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- McCormick, C.A., Griffin, H.G., Underwood, H.M. & Gasson, M.J.1998. Common DNA sequences with potential for detection of genetically manipulated organisms in food. Journal of Applied Microbiology 84, 969-980.
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- McCormick, C.A., Griffin, H.G., Underwood, H.M. & Gasson, M.J. 1998. Common DNA sequences with potential for detection of genetically manipulated organisms in food. Journal of Applied Microbiology 84, 969-980.
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-Recombinant DNA technology: Restriction enzymes. Cloning and sequencing. Biotechnology and its implications for Society.
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-Concepto de mutación. Mutación génica. Mutaciones cromosómicas (numéricas y estructurales). Aplicaciones de la mutación en Mejora genética.
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Sequence-Selective DNA Recognition with Peptide–Bisbenzamidine Conjugates
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Sequence-Selective DNA Recognition with Peptide–Bisbenzamidine Conjugates
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Unit 9. Bacterial genetics. DNA structure. Genetic material of bacteria. Genetic variation. Genetic mutation and transference.
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Tema 9. Xenética bacteriana I. Estrutura do ADN. O material xenético das bacterias. Variación xenética. Mutación e transferencia xenética.
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Clone vector DNA
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ADN clonado en vectores
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ADN clonado en vectores
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DNA Sequencing
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Secuenciación de ADN
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Secuenciación de ADN
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*Ask for other DNA types
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*Para otros tipos de ADN consultar
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*Para outros tipos de ADN consultar
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LESSON 4. DNA CLONING IN E. coli (2h 30 ')
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TEMA 7. SECUENCIACIÓN DEL DNA. (2h)
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DNA Type
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Tipo de ADN
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Tipo de ADN
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LESSON 7. DNA SEQUENCING. (2h)
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TEMA 10. INGENIERÍA GENÉTICA CON LEVADURAS. (2h)
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LESSON 11. DNA CLONING IN ANIMAL CELLS. (2h)
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TEMA 14. BIOTECNOLOGÍA APLICADA A LA MEDICINA. (2h)
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LESSON 2. RECOMBINANT DNA ENZYMOLOGY. (2h)
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TEMA 5. GENOTECAS Y MICROARRAYS. (2h)
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To understand the fundaments of the DNA manipulation. To be familiarized with the molecular techniques of DNA detection and proteins.
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Entender los fundamentos de la manipulación de ADN. Estar familiarizado con las técnicas moleculares de detección de ADN y proteínas.
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2) Manipulation methods of DNA in foods.
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2) Métodos de manipulación de ADN en alimentos
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To understand the fundaments of the DNA manipulation. To be familiarized with the molecular techniques of DNA detection and proteins.
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Entender los fundamentos de la manipulación de ADN. Estar familiarizado con las técnicas moleculares de detección de ADN y proteínas.
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7) Recombinant DNA Technology in the food production.
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7) La tecnología del ADN recombinante en la producción de alimentos
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5) DNA chips and microarrays for the food industry.
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5) Chips de DNA y microarrays para la industria alimentaria
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5) Technology security of the recombinant DNA.
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5) Seguridad de la tecnología del DNA recombinante
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7) Visual display of amplificated DNA.
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8) Tratamiento de las muestras con enzimas de restricción
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3) Control molecular methods of food: DNA and proteins analyses.
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3) Métodos de control molecular de alimentos: análisis de ADN y de proteínas.
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Knowledge of DNA manipulation.
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Destrezas requeridas:
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4) Visual display of extracted DNA in agarose gel.
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5) Selección in-silico de enzimas de restricción para PCR-RFLP
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Angew. Chem. publish our work on DNA association dynamics
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Angew. Chem. publica nuestro trabajo sobre dinámica de asociación del ADN
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If PCR products are not purified it must be specified. This means a higher cost and a delay in the delivery of results. It is important that users make sure of the presence of a unique DNA band.
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Si los productos de PCR no están purificados debe especificarlo, esto supondrá un coste a mayores y una demora en la entrega de resultados. Es importante que el usuario se haya cerciorado de la presencia de un único ADN molde.
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Se os produtos de PCR non están purificados debe especificalo, isto suporá un custo a maiores e unha demora na entrega de resultados. É importante que o usuario se tivera cerciorado da presenza dun único ADN molde.
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In the case of purified PCR products 1,5µl of specific primer will be sent to a concentration of 5µM per sample, and 10 µl of DNA. The recommended concentration of the sample can be consulted in the following table:
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En el caso de productos de PCR purificados por el usuario se enviará 1,5µl de primer específico a una concentración de 5µM por muestra, y 10 µl de ADN. La concentración recomendada a la que debe estar la muestra puede consultarse en la siguiente tabla:
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No caso de produtos de PCR purificados polo usuario enviarase 1,5µl de primer específico a unha concentración de 5µM por mostra, e 10 µl de ADN. A concentración recomendada á que debe estar a mostra pode consultarse na seguinte táboa:
  Temporary electrostatic...  
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Temporary electrostatic impairment of DNA recognition: light-driven DNA binding of Peptide dimers
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A. Jiménez-Balsa, E. Pazos, B. Martínez-Albardonedo, J.L. Mascareñas, M.E. Vázquez
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-Seminar 3. DNA sequencing techniques. (1h)
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