Bands dark on sides and light in middle
Posted 27 September 2012 - 08:34 PM
Has anyone ever had this problem, or have any idea about what might be causing it? I've tried using lower and higher percentage gels, running at a lower voltage, making all new buffers, trying different types of loading buffers, etc., but nothing seems to solve the problem. Please help!
Posted 28 September 2012 - 05:04 PM
Posted 29 September 2012 - 01:14 AM
You can try to do a colorimetric development using TMB and see if you get better resolved bands. Or you can ponceau stain the blot before blocking and see if the bands look normal there.
Edited by cbf88, 29 September 2012 - 01:16 AM.
Posted 01 October 2012 - 04:31 PM
I get the same results when I use different primary and secondary antibodies, so I don't think it's the antibodies. Also, when I do longer exposures, I will get solid, dark bands, but they're overexposed. I need my bands to be in the linear range so I can quantify them, but when they're in the linear range, they have this dumbbell shape, which makes them difficult to quantify.
Posted 01 October 2012 - 05:53 PM
Isn't fibronectin ~400kDa in size? From my knowledge, it's a huge glycoprotein. Would be good if you double checked your antibody specification sheet.
How did your loading control turn out? I.e. housekeeping proteins such as tubulin, actin or GAPDH?
What kind of SDS-PAGE gel did you use? homemade or commercial?
Posted 03 October 2012 - 09:39 AM
My GAPDH looks fine, with solid bands even at the lightest exposures. All of the bands in my marker look normal too. In fact, every other protein I run yields normal-looking bands, except for this one.
We make our own gels. Because of the large size of the protein, I usually run a 5%/3% or 6%/4% resolving/stacking gel, and I always make sure the stacking gel is at least 1X the height of the well. I sometimes run a 8%/4% gel, and the edges of the bands are still noticeably darker than the middle, though it's less pronounced.
Posted 03 October 2012 - 10:08 AM