Anomalous signal even with room temperature capillary data was measurable on 
diffractometers and early area detectors.
However there were misspellings in  software packages such as sending anomalous 
phase 90deg into the wrong direction
in one of them or others. 
After in-house editing, anomalous signal contributed significantly. It was also 
very instrumental in discovering mis-setings in 
formats of area detectors. We have used a method as appeared in  Tom Blundell 
and Louise Johnson  unrivaled book 
Protein Crystallography ( I own one!) by checking the peaks of the second 
derivatives with  the phases of the first derivative with the contribution of 
correct or inverted anomalous signal contribution to get correct detector 
format or space group or else. I still have a logbook that keep records of 
getting out correct Xentronics format. So no fiction, just errors… Physics 
works!!! 
FF


Dr Felix Frolow   
Professor of Structural Biology and Biotechnology
Department of Molecular Microbiology
and Biotechnology
Tel Aviv University 69978, Israel

Acta Crystallographica F, co-editor

e-mail: [email protected]
Tel:  ++972-3640-8723
Fax: ++972-3640-9407
Cellular: 0547 459 608

On Jun 6, 2012, at 18:02 , Dyda wrote:

>> I suspect that pure MIR (without anomalous) was always a fiction. I doubt 
>> that anyone has ever used it. Heavy atoms always give
>> an anomalous signal
> 
>> Phil
> 
> I suspect that there was a time when the anomalous signal in data sets was 
> fictional.
> Before the invent of flash freezing, systematic errors due to decay and the 
> need
> of scaling together many derivative data sets collected on multiple crystals 
> could render
> weak anomalous signal useless. Therefore MIR was needed. Also, current 
> hardware/software
> produces much better reduced data, so weak signals can become useful.
> 
> Fred
> 
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