logging in or signing up Electrophoresis kcjstaine Download Post to : URL : Related Presentations : Let's Connect Share Add to Flag Embed Email Send to Blogs and Networks Add to Channel Copy embed code: Embed: Flash iPad Dynamic Copy Does not support media & animations Automatically changes to Flash or non-Flash embed WordPress Embed Customize Embed URL: Copy Thumbnail: Copy The presentation is successfully added In Your Favorites. Views: 9711 Category: Education License: All Rights Reserved Like it (4) Dislike it (0) Added: November 26, 2008 This Presentation is Public Favorites: 2 Presentation Description gel electrophoresis Comments Posting comment... By: avana (24 month(s) ago) hello Mr. Kevin -- plz send to me this ppt Saving..... Post Reply Close Saving..... Edit Comment Close By: hosam1 (28 month(s) ago) Plz send me this ppt Saving..... Post Reply Close Saving..... Edit Comment Close By: kkn123 (38 month(s) ago) Plz send me this ppt. Saving..... Post Reply Close Saving..... Edit Comment Close By: ranajeet (40 month(s) ago) please allow me to download this ppt....i need it...plzzzz.... Saving..... Post Reply Close Saving..... Edit Comment Close By: kh1s (40 month(s) ago) plz allow me dowload this presentation? Saving..... Post Reply Close Saving..... Edit Comment Close loading.... See all Premium member Presentation Transcript Slide 1: Gel Electrophoresis Slide 2: What is Gel Electrophoresis? Gel electrophoresis separates molecules on the basis of their charge and size. The charged macromolecules migrate across a span of gel because they are placed in an electrical field. The gel acts as a sieve to to retard the passage of molecules according to their size and shape. BIOTECHNOLOGY : BIOTECHNOLOGY One of the basic tools of modern biotechnology is gene splicing. This is the process of removing a functional DNA fragment ( a gene) from one organism and combining it with the DNA of another organism to study how the gene works. The desired result is to have the new organisms carry out the expression of the gene that has been inserted. Restriction Enzymes : Restriction Enzymes The ability to cut and paste DNA predictably is due to the use of restriction enzymes. They were first identified in and isolated from the bacteria that use them as a natural defense mechanism to cut up the invading DNA of bacteriophages – viruses that infect bacteria. They are named for the Slide 5: The negatively charged particles move toward the positive electrode while the the positive charge particles move toward the negative electrode. Slide 6: How does electrophoresis work? The gel is made from agar DNA is a negative molecules Molecules sort based on Charge Size shape What is agar? : What is agar? Agar comes from sea weed. What is it used for? The gel is 1% agarous and has no electrical charge. How does it work? : How does it work? DNA is cut into smaller fragments. Loading dye is used to indicate the fragments of DNA are behind the dye The negative DNA molecule is attracted to the positive electrode. The smallest fragments move the greatest distance. Procedure : Procedure Remove comb and observe wells. Place carbon paper in each end of the tray. Cover with buffer, making sure the allow buffer to overflow into each end of the tray. Load gels. Connect the electrodes. Turn on power supply. Allow gels to run – make sure you see bubbles coming from the electrodes. PROCEDURE (CONTINUED) : PROCEDURE (CONTINUED) It will take about 30 minutes for the gel to run. Turn off power supply and remove electrodes. Pour off buffer into the designated container. Carefully remove gel from gel box and place in glad container and cover with stain. Store in appropriate location. What is significant about the bubbles? : What is significant about the bubbles? They indicate that electrolysis of water is taking place. One electrode will have a lot of bubbles and the other will have a lesser amount. Why the difference? The formula for water is H2O and the splitting of the molecule will produce twice as many atoms of hydrogen. You do not have the permission to view this presentation. In order to view it, please contact the author of the presentation.