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Topic: Two internal standards - Why?  (Read 3945 times)

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Offline Telamond

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Two internal standards - Why?
« on: November 03, 2008, 02:18:56 PM »
So during one of the experiments we were doing, we used two IS, which I found pretty weird.
Is there any use for two IS?

Offline wpenrose

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Re: Two internal standards - Why?
« Reply #1 on: November 03, 2008, 04:06:34 PM »

You'd have to give more info on the experiment. Sometimes, one internal standard is used to determine yield, the other to calibrate a mass spectrum or a retention time in a gas chromatographic analysis.
eg
http://www.imss.nl/imsc17/abstracts/abstract3fe0.html?ID=411

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Offline JGK

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Re: Two internal standards - Why?
« Reply #2 on: November 05, 2008, 05:51:32 PM »
How many Analytes were you quantifying?

If there were 2 analytes with differing properties, a separate IS may be used for each of the analytes.
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Offline Telamond

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Re: Two internal standards - Why?
« Reply #3 on: November 06, 2008, 03:18:17 PM »
Yes, we had several analytes, it was the metabolites of limonene.
The retention time for them separated was maybe >6 mins as well, so I'd guess that two IS would be needed. IS1 eluted out first and IS2 eluted out last.
What I learned from a lab assistent was that ideally, one would have one IS per analyte, but that seemed a bit overkill as well. :o

Odd thing was that they wrote in the instructions to only use IS2 for quantification...

Thank you for the replies, both of you. :)


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