Jump to content

  • Log in with Facebook Log in with Twitter Log in with Windows Live Log In with Google      Sign In   
  • Create Account

Submit your paper to J Biol Methods today!
Photo
- - - - -

Laemmli Buffer Problems


  • Please log in to reply
2 replies to this topic

#1 kmwalters

kmwalters

    member

  • Members
  • Pip
  • 1 posts
0
Neutral

Posted 19 May 2010 - 12:17 PM

When running western blots of samples which have been boiled in laemmli buffer, occasionally my bands will collapse into a thin line, rather than a full lane, making it impossible to make sense of the gel. What am I doing wrong?

#2 lab rat

lab rat

    Why does a science forum not have pictures of mice and rats?

  • Active Members
  • PipPipPipPipPipPipPipPipPipPip
  • 245 posts
7
Neutral

Posted 19 May 2010 - 12:23 PM

Let me see if I understand your description correctly: instead of fat, separated bands, you get one thin, run-together one? Or are they separate and thin?

Maybe your (precast?) gel is old, or something on the plates is preventing the gel from adhering well. You could be getting slow leakage around the edge of the gel.
42..."An immutable fixed-precision number of unlimited magnitude." <a href="http://en.wikipedia....amming_language)" target="_blank">http://en.wikipedia....amming_language)</a>, accessed 25June2009.

#3 fishdoc

fishdoc

    Veteran

  • Active Members
  • PipPipPipPipPipPipPipPipPipPip
  • 272 posts
2
Neutral

Posted 19 May 2010 - 03:05 PM

When running western blots of samples which have been boiled in laemmli buffer, occasionally my bands will collapse into a thin line, rather than a full lane, making it impossible to make sense of the gel. What am I doing wrong?




DNA in the sample maybe? I've been doing boil preps for westerns with bacterial cultures and have noticed if the samples I load are too concentrated, it looks like there is a string down the middle of the lanes that the proteins stick to that causes a distortion in the band. Instead of being a nice uniform band, it turns almost into a "W" shape or something along those lines. I don't know for sure what causes that, but assumed it may be DNA from the prep, or some other cellular debris. If I sonicate the pellets instead of boiling, I can get a higher concentration without the distortion. I've read that the sonication breaks up the DNA a lot better than the boiling does. I'll see if I can find an image of one of my gels or westerns to show the distorted bands.


Here is a band from western... doing a coomassie of a gel basically looks the same, but with all bands like that, not just the one.

Attached Thumbnails

  • distortion.jpg

Edited by fishdoc, 19 May 2010 - 03:11 PM.





Home - About - Terms of Service - Privacy - Contact Us

©1999-2013 Protocol Online, All rights reserved.