WHY DON'T WE FREEZE 35-S AUTORADS ?
user at mac-biocomputing2.EMBL-Heidelberg.DE
Sat Nov 23 11:56:16 EST 1996
Hi ...this week I followed the "cool" discussion about why do we freeze
autorads and while I was reading all the answers I was wondering why
don't we freeze autorads when we expose dried polyacrilammide gel for
sequencing where the isotope used is usually 35-S instead of 32-P !!!???
1) It depends on the physical-chemical properties of the gel that might
crash at highest low temperature ......?
2) It is a metter of the particular isotope (35-S or 32-P) and so of the
different decay and particles emitted
I would appreciate any suggestion....thanks !
corona at EMBL-Heidelberg.DE
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