1. Notes: 605 / 3 weeks ago  from sciencesoup
    If you like Gel Electrophoresis you will like my AGE-themed parody video! https://www.youtube.com/watch?v=20Dzhj9VFsU
sciencesoup:

Gel Electrophoresis
There’s a cool experiment you can do with DNA, and you only really need to know one thing: it’s a negatively charged molecule, since phosphate is negatively charged and DNA is largely made up of its sugar-phosphate backbone. The experiment is called Gel Electrophoresis, and essentially, it separates molecules based on size. Biologists use it to figure out the size of a DNA samples by seeing how far they move through a substance as compared to how far DNA fragments of known size move through the same substance.
A common substance is agarose gel, which can be easily set on a glass slide. While it’s setting, you create little wells in one end—pockets to insert your DNA into later. Usually you’ll have several samples of DNA of varying, unknown sizes combined with loading buffer, which weighs down your sample so it stays comfortably in the gel.

(Source: Wikimedia Commons)
To get started, your gel is placed into a gel electrophoresis chamber, which is essentially just a tank where you can apply a voltage and create an electric field. Running buffer is added to the tank to cover the gel, and then you insert your DNA samples into the wells. You also have a sample of DNA fragments of known size, and you usually put those on either side of your unknown samples so you can compare later.

(Source: camerazn)
When you apply a voltage across the tank, the DNA will start to move—the pores of the agarose gel act like a sieve. Since DNA is negatively charged, it will be repulsed from the negative end of the tank and migrate through the gel towards the positive end. The fragments travel parallel to each other in lanes: smaller fragments travel faster and further, and the longer fragments travel slower.
Eventually, some of the smaller molecules will have travelled all the way through the gel, and you should turn off the voltage. But at this point, you can’t clearly see where they all are, since they’re so small. So after applying a voltage, you remove the gel and stain it. Under UV light, it will be flurorescent—so voila, you can take an picture and you should see something like this:

(Source: Wikimedia Commons)
On the far left you can see the known sample, and by doing a little bit of maths and comparison, you can figure out the sizes of your DNA fragments.
Gel electrophoresis is has a bunch of applications in forensics, microbiology, genetics, biochemistry and molecular biology.
Further resources: Interactive explorations of the experiment here and here, and a more detailed look at the process from Osmania University

    If you like Gel Electrophoresis you will like my AGE-themed parody video! https://www.youtube.com/watch?v=20Dzhj9VFsU

    sciencesoup:

    Gel Electrophoresis

    There’s a cool experiment you can do with DNA, and you only really need to know one thing: it’s a negatively charged molecule, since phosphate is negatively charged and DNA is largely made up of its sugar-phosphate backbone. The experiment is called Gel Electrophoresis, and essentially, it separates molecules based on size. Biologists use it to figure out the size of a DNA samples by seeing how far they move through a substance as compared to how far DNA fragments of known size move through the same substance.

    A common substance is agarose gel, which can be easily set on a glass slide. While it’s setting, you create little wells in one end—pockets to insert your DNA into later. Usually you’ll have several samples of DNA of varying, unknown sizes combined with loading buffer, which weighs down your sample so it stays comfortably in the gel.

    image

    (Source: Wikimedia Commons)

    To get started, your gel is placed into a gel electrophoresis chamber, which is essentially just a tank where you can apply a voltage and create an electric field. Running buffer is added to the tank to cover the gel, and then you insert your DNA samples into the wells. You also have a sample of DNA fragments of known size, and you usually put those on either side of your unknown samples so you can compare later.

    image

    (Source: camerazn)

    When you apply a voltage across the tank, the DNA will start to move—the pores of the agarose gel act like a sieve. Since DNA is negatively charged, it will be repulsed from the negative end of the tank and migrate through the gel towards the positive end. The fragments travel parallel to each other in lanes: smaller fragments travel faster and further, and the longer fragments travel slower.

    Eventually, some of the smaller molecules will have travelled all the way through the gel, and you should turn off the voltage. But at this point, you can’t clearly see where they all are, since they’re so small. So after applying a voltage, you remove the gel and stain it. Under UV light, it will be flurorescent—so voila, you can take an picture and you should see something like this:

    image

    (Source: Wikimedia Commons)

    On the far left you can see the known sample, and by doing a little bit of maths and comparison, you can figure out the sizes of your DNA fragments.

    Gel electrophoresis is has a bunch of applications in forensics, microbiology, genetics, biochemistry and molecular biology.

    Further resources: Interactive explorations of the experiment here and here, and a more detailed look at the process from Osmania University

     
  2. Comments
  3. 1 month ago 

    I just finished a parody music video of Robin Thicke’s “Blurred Lines” all about Gel Electrophoresis. No matter how you feel about the original video or song, if you like #SCIENCE, genetics, and lab work, you will probably like #BLURREDBANDS!

  4. Comments
  5. Notes: 1 / 3 months ago  from srkinblackandwhite
    srkinblackandwhite:

I am heading off to medical school shortly, so this was my last comic for the Yale Daily News. No joke on this one, just my heartfelt thanks for the readers who have enjoyed my comic strip the past 5 years.
I may have time to keep making cartoons in med school, but it won’t be on a syndicated schedule like these were. Therefore, “Science Hill” is going on hiatus, and leaving the Yale Daily News this semester.
Thank you! (25April2014)

FYI, this strip features the brand new font, Comic Neue, which I believe is still free for a limited time: http://comicneue.com/

    srkinblackandwhite:

    I am heading off to medical school shortly, so this was my last comic for the Yale Daily News. No joke on this one, just my heartfelt thanks for the readers who have enjoyed my comic strip the past 5 years.

    I may have time to keep making cartoons in med school, but it won’t be on a syndicated schedule like these were. Therefore, “Science Hill” is going on hiatus, and leaving the Yale Daily News this semester.

    Thank you! (25April2014)

    FYI, this strip features the brand new font, Comic Neue, which I believe is still free for a limited time: http://comicneue.com/

     
  6. Comments
  7. Notes: 1 / 3 months ago 
    I am heading off to medical school shortly, so this was my last comic for the Yale Daily News. No joke on this one, just my heartfelt thanks for the readers who have enjoyed my comic strip the past 5 years.

I may have time to keep making cartoons in med school, but it won’t be on a syndicated schedule like these were. Therefore, “Science Hill” is going on hiatus, and leaving the Yale Daily News this semester.
Thank you! (25April2014)

    I am heading off to medical school shortly, so this was my last comic for the Yale Daily News. No joke on this one, just my heartfelt thanks for the readers who have enjoyed my comic strip the past 5 years.

    I may have time to keep making cartoons in med school, but it won’t be on a syndicated schedule like these were. Therefore, “Science Hill” is going on hiatus, and leaving the Yale Daily News this semester.

    Thank you! (25April2014)

    (Source: yaledailynews.com)

     
  8. Comments
  9. 3 months ago 
    Didn’t get to post this last week because things were a little too freaky-deaky. (14Apr14)

    Didn’t get to post this last week because things were a little too freaky-deaky. (14Apr14)

    (Source: yaledailynews.com)

     
  10. Comments
  11. 3 months ago 
    About a month ago I was invited by the Yale Record humor magazine (to which I submitted cartoons as an undergrad) to help them create a full-scale parody issue of the Yale Daily News. The issue came out this past Thursday and is excellent in every way. I am proud to have my self-parody meta-comics appear in the issue and honored to be lampooned in the “advertisement” above. You can click through the picture to see the full “Yale Daily Record” issue. (10Apr14)

    About a month ago I was invited by the Yale Record humor magazine (to which I submitted cartoons as an undergrad) to help them create a full-scale parody issue of the Yale Daily News. The issue came out this past Thursday and is excellent in every way. I am proud to have my self-parody meta-comics appear in the issue and honored to be lampooned in the “advertisement” above. You can click through the picture to see the full “Yale Daily Record” issue. (10Apr14)

     
  12. Comments
  13. 3 months ago 
    I guess that makes Yale racemic (7Apr14).

    I guess that makes Yale racemic (7Apr14).

    (Source: yaledailynews.com)

     
  14. Comments
  15. Notes: 1 / 4 months ago 
    Everybody clap your hands (26Mar13)

    Everybody clap your hands (26Mar13)

    (Source: yaledailynews.com)

     
  16. Comments
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