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low recovery / protein loss in the lower range..

Discussions about HPLC, CE, TLC, SFC, and other "liquid phase" separation techniques.

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amount depends on chromophores (I don't know if spelling's good) area is usually few millions for 100%
for smaller concentration few hundreds is usually good
area units.. milli Au units* seconds..

i use an agilent detection system.. 210 or 215 detection wavelength..
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alicee, if you have been following this forum long enough you will know that I use radiodetection, among others, thus I have worked with extremely low concentrations. That is not the point, however. If I can´t hack an analysis I clearly state that. As I said, in my position it has been possible to proceed after evaluating that an estimation was of value.

Incidentally, I have not encountered a HPLC column or TLC plate which doesn´t smear out the radioactivity. This has been usually at such low amounts that in "normal" detection it is not a problem. I am talking about "simple" ions, like 36-Cl-, amino acid, peptides, and proteins.
17 posts Page 2 of 2

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