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Gel loading and electrophoresis

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Uploaded by on Apr 7, 2009

No sound. Gel loading and time-lapse of a 1% agarose gel for DNA.

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Education

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Standard YouTube License

  • likes, 1 dislikes

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Uploader Comments (gkpeter)

  • Your way is very sloppy. like your pipping method.

  • @volleyball994pimp When you have time, please explain the other ways to load the gel. This actually was a student of mine and I thought it was pretty good. If there are other ways to load gels, I would be interested in knowing.

  • @gkpeter Really, that is too bad you graded on something as insignificant as that. It is a dye, so there is very little DNA in there to throw off results. In real life in a real lab, that amount of "spillage" is fairly insignificant. When you load a gel with 96 samples, you don't have a lot of time to worry about "spillage". Just my two cents worth. :)

  • I do have another video that is similar and has sound. This initially was a trial.

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All Comments (13)

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  • great video

  • @Volleyball994pimp

    This was a good video, not sure what you're talking about when you say she got gel everywhere. The "gel" was already made and the "sample" is what was being loaded. I do this in my lab when conducting RT-PCR and it's not unusual to have sample expel from the well when loading, which doesn't hurt the running of the gel because it is released into the buffer.

    Adam (Microbiology and Immunology Masters Program)

    Boonshoft School of Medicine

    Wright State University

  • @neverowned1 im doing it tomorrow too! . . . a year after you are (:

  • Amazing, you beat the trolls at their own game and they stop talking? For the record, "pipping" is spelled piping or pipetting.

  • @gkpeter not a diffrent way to load the gel it's just that she got the gell everywere. in my class that wouldnt be grade A work. i just think she made a mess when loading the gels.

  • Great video! Thanks alot!

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