harwoods at AVA.BCC.ORST.EDU
Wed Apr 26 23:12:38 EST 1995
On 25 Apr 1995, Biology Department wrote:
> Recently, our gels have been running slanted--if you view the gel
> from the side the bands are diagonal to the horizontal plane of the gel.
> We have remade our buffer (1XTAE) but this does not seem to help. Any
> suggestions as to the cause of this problem? The major difficulty is
> that if you view the gels from above the bands appear fuzzy and wide
> instead of sharp. Any comments would be appreciated.
I've had the same experience. I have had some success adjusting my
methods with regard to the following considerations:
1. Too much DNA per band. Sambrook et al. 1989 suggest that 0.8 ug DNA
is the most that can be satisfactorily resolved in a 0.5 cm band. To try
to get the smaller bands, I tend to overload my lanes, especially with
2. Electric field too strong.
3. Sample loaded too high in the wells. When pouring horizontal gels,
the meniscus around the combs causes the well to be deeper than the
actual slab. The sample shouldn't be deeper than the slab itself.
Hope this helps.
Dept. Ag. Chem.
Oregon State University
Corvallis, OR 97331
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