1 / 15

Chapter 28

Chapter 28. Manipulating DNA. Chapter Objectives. Know how the techniques of molecular biology work Understand how to use the tools of molecular biology Put it all together with a molecular biology project (we will work on this in class after we know the tools and techniques). Techniques.

ghalib
Télécharger la présentation

Chapter 28

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Chapter 28 Manipulating DNA

  2. Chapter Objectives • Know how the techniques of molecular biology work • Understand how to use the tools of molecular biology • Put it all together with a molecular biology project (we will work on this in class after we know the tools and techniques)

  3. Techniques • Restriction Enzymes • Electrophoresis • Hybridization probes • DNA sequencing • Chain terminator • Automated • Emulsion • PCR

  4. Restriction Enzymes • https://www.neb.com/products/restriction-endonucleases • App: Search NEB tools in either play store or App store • Remember overhangs, this will be important

  5. Electrophoresis Polyacrylamide Agarose

  6. Hybridization Probes • Northern Blot – RNA detection • Southern Blot – DNA detection • Western Blot – Protein detection

  7. DNA Sequencing • Chemical Sequencing • Chain Terminator (dideoxy nucleotides) • Automated (color) • Emulsion

  8. PCR 55? annealing 72 elongate 95 denature repeat

  9. Tools • RT-PCR • Microarray • Cloning • Plasmids • Bacteriaphage • Cosmids • BAC/YAC • Site-directed mutagenesis • Knockout mice

  10. Real-time (kind of) PCR(qPCR) (sort of) • Can quantify the exact about of mRNA using PCR • Combine dsDNA binding dye with PCR

  11. Microarrays

  12. Cloning • Plasmid – small, circular DNA – can hold about 10 kb • Bacteriophage – larger, circular DNA – can hold about 20 kb • Cosmid – combination of a plasmid and phage, can hold 40-50 kb • BAC/YAC – bacterial artificial chromosome/yeast AC – can hold up to 500 kb

  13. Site Directed Mutagenesis • Change DNA in plasmid, etc. to make a mutation in protein (substitution/deletion) • Can change any residue to any other residue • Implications?

  14. Mice • Knockout • Deletion of gene • Knockin • Insertion of gene • Genetic background • models

  15. Active Learning • Projects • Download serial cloner • http://serialbasics.free.fr/Serial_Cloner.html • Build plasmids (learn about functions) • Create (on paper) a mutant protein • Create an experiment to study your protein • Learn about creating knockout mice.

More Related