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Recombinant DNA Techniques chapter 18 Part I techniques and their applications. 1. Restriction Digest (to be done in lab) 2.Southern Blot 3.Northern.

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Presentation on theme: "Recombinant DNA Techniques chapter 18 Part I techniques and their applications. 1. Restriction Digest (to be done in lab) 2.Southern Blot 3.Northern."— Presentation transcript:

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2 Recombinant DNA Techniques chapter 18 Part I

3 techniques and their applications. 1. Restriction Digest (to be done in lab) 2.Southern Blot 3.Northern Blot 4.Western Blot 5.Cloning

4 1. Restriction Digest: The Cutting of DNA Endonucleases = Restricition Enzymes

5

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7 EXAMPLES OF DNA AGAROSE GELS Ladder, marker or standard of known DNA sizes

8 An Application of Restriction Digest Chromosomal Disorders

9 Put your thinking cap on!

10 Wild type Hb Sickle cell Hb Restriction enzyme loss of cutting site 1 band is too small to view here) 23

11 Wt Wt M M Wt= wildtype M= mutated

12 An Application to Forensic & Paternity Studies 2. The Southern Blot

13 1. Restriction Digest & gel electrophoresis TRANSFER DNA victim DNA suspect 1 DNA suspect 2 DNA crime scene

14 You must understand the reason for the “probe”!

15 But there are thousands of fragments!

16 So sometimes you have to really search for the differences between DNA.

17 Probe is complementary “hot” DNA

18 SUMMARY OF A SOUTHERN BLOT From: Restriction digest To result

19 Victim Suspect 1Suspect 2Crime scene Back to our crime scene

20 Techniques also are available to measure RNA and Protein 3. Northern Blot for RNA4. Western Blot for Protein

21 Western Southern Northern Summary: Blotting techniques with probes

22 5. Technique: Cloning of specific genes or DNA fragments + = restriction enzyme = ligase

23 Cut vector Cut foreign DNA or gene Paste together

24 2 different antibiotic resistant genes Bacteria are now resistant to 2 antibiotics

25 Let’s apply these concepts to plasmid transformation.

26 Cut DNA here & insert foreign DNA

27 Will your transformed colonies with the insert be white or blue?

28 Summary of cloning DNA into a blue/white selection vector

29 End of part 1


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