A readable but not aesthetic sequencing gel
leach at mbcrr.harvard.edu
Tue May 3 22:34:58 EST 1994
In article <Cp7pEw.FDo at umdnj.edu>, bawagan at umdnj.edu (Hinayana Bawagan)
> My sequencing gels can give me the information I want but they are not
> beautiful. I just hate this. I get lanes that tend to constrict. I do blow
> the airbubbles off the wells to remove the urea with a glass pipette. As
> soon as the temp is around 50, I load the samples but not fast enough to keep
> the temp from dipping to below 45.
Denature them 80C for ten minutes then place them on ice rapidly. Then load
I have trouble reusing the same tip when
> others in my lab can just use one and seldom get it clogged.
I use a new tip everytime - (i also chop sequioa (typo?) daily and dont
recycle polystyrene packages)
> I am using the Sequenase Version 2 kit. Anyone out there can give me
> their reliable bag of tricks that you can not get from a book but can only
> be learned from experience.
> Thank you.
Well i find the trick is to always load from my left hand while wearing one
red and one blue converse sneaker. A waxing moon or a month with an R in it
usually helps (although i put the latter down to superstition).
Martin 'too much caffeine today' Leach
..... Martin Leach Email:leach at mbcrr.harvard.edu
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