Agarose gel electrophoresis

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Esta presentación la encontré en la web y entiendo que es muy útil para la práctica de Electroforesis de Gel Agarosa. Explica de forma básica de que consta esta tecnica molecular y los pasos a seguir.

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Agarose gel electrophoresis

  1. 1. CSS451 CSS/HRT 451AGAROSE GEL ELECTROPHORESIS Wells Guo-qing Song And David Douches Guo-qing
  2. 2. CSS451 OUTLINEConceptApplicationsFactors affecting Migration 1. DNA or RNA Molecular Weight 2. Voltage 3. Agarose 4. Buffer 5. VisualisationEquipments and Supplies
  3. 3. CSS451 ConceptAgarose gel electrophoresis: A method used in biochemistry and molecular biology to separate DNA or RNA molecules by size. This is achieved by moving negatively charged nucleic acid molecules through an agarose matrix with an electrotric field (electrophoresis). Shorter molecules move faster and migrate farther than longer ones. Sambrook J, Russel DW (2001). Molecular Cloning: A Laboratory Manual 3rd Ed. Cold Spring Harbor Laboratory Press. Cold Spring Harbor, NY
  4. 4. CSS451 ApplicationEstimation of the size of DNA moleculesAnalysis of PCR products, e.g. in molecular geneticdiagnosis or genetic fingerprintingSeparation of restricted genomic DNA prior to Southern analysis, or of RNA prior to Northern analysis.
  5. 5. CSS451Restriction mapping of cloned DNA
  6. 6. CSS451PCR products in genetic diagnosis
  7. 7. CSS451Southern analysis—DNA transfer After Before
  8. 8. CSS451Southern Hybridization
  9. 9. CSS451 Northern Analysis RNAHybridization
  10. 10. CSS451 Factors affecting Migration1. DNA or RNA Molecular Weight2. Voltage3. Agarose4. Buffer5. Visualisation
  11. 11. CSS4511. DNA or RNA Molecular Weight The length of the DNA molecule is the most important factor, smaller molecules travel farther.2. Voltage The higher the voltage, the faster the DNA moves. But voltage is limited by the fact that it heats and ultimately causes the gel to melt. High voltages also decrease the resolution (above about 5 to 8 V/cm)
  12. 12. CSS4513. AgaroseAgarose gel electrophoresis can be used for the separation of DNA fragments ranging from 50 base pair to several megabases (millions of bases) using specialized apparatus. Increasing the agarose concentration of a gel reduces the migration speed and enables separation of smaller DNA molecules.The distance between DNA bands of a given length is determined by the percent agarose in the gel. In general lower concentrations of agarose are better for larger molecules because they result in greater separation between bands that are close in size. The disadvantage of higher concentrations is the long run times (sometimes days). Instead high percentage agarose gels should be run with a pulsed field electrophoresis (PFE), or field inversion electrophoresis.Most agarose gels: 1. 1% gels are common for many applications. 2. 0.7%: good separation or resolution of large 5–10kb DNA fragments 3: 2% good resolution for small 0.2–1kb fragments. 4: Up to 3% can be used for separating very tiny fragments but a vertical polyacrylamide gel is more appropriate in this case.
  13. 13. CSS4514. BufferThe most common buffers for agarose gel:TAE: tris acetate EDTATBE: Tris/Borate/EDTASB: Sodium borate.TAE has the lowest buffering capacity but provides the best resolution forlarger DNA. This means a lower voltage and more time, but a better product. Brody JR, Calhoun ES, Gallmeier E, Creavalle TD, Kern SE (2004). Biotechniques. 37:598- 602.
  14. 14. CSS4515. Visualisation The most common dye used to make DNA or RNA bands visible for agarose gel electrophoresis is ethidium bromide, usually abbreviated as EtBr. It fluoresces under UV light when intercalated into DNA (or RNA). By running DNA through an EtBr-treated gel and visualizing it with A pattern of DNA-bands under UV light UV light, any band containing more than ~20ng DNA becomes distinctly visible. EtBr is a known carcinogen, however, and safer alternatives are available. A color marker dye containing a low molecular weight dye such as "bromophenol blue" (to enable tracking the progress of the electrophoresis) and glycerol (to make the DNA solution denser so it will sink into the wells of the gel).
  15. 15. CSS451 Equipments and Supplies•Buffer solution, usually TBE buffer or TAE 1.0x, pH 8.0•Agarose•An ultraviolet-fluorescent dye, ethidium bromide, (5.25 mg/ml in H2O).Alternative dyes may be used, such as SYBR Green.•Nitrile rubber gloves. Latex gloves do not protect well from ethidiumbromide•A color marker dye containing a low molecular weight dye such as"bromophenol blue“•A gel rack•A "comb“•Power Supply•UV lamp or UV lightbox or other method to visualize DNA in the gel
  16. 16. CSS451
  17. 17. CSS451 Advantages & DisadvantagesThe advantages are that the gel is easily poured, doesnot denature the samples. The samples can also berecovered.The disadvantages are that gels can melt duringelectrophoresis, the buffer can become exhausted, anddifferent forms of genetic material may run inunpredictable forms. After the experiment is finished,the resulting gel can be stored in a plastic bag inrefrigerater.
  18. 18. All the ethidium bromide-contaminated waste needs to bedisposed through the ORCBS.

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