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Plasma samples were prepared according to different protocols in order to analyze the effect of sample preparation on interference of proteotypic peptides.
Plasma samples were prepared for 1H NMR spectroscopy with minimal handling as described [12].
The plasma samples were prepared by diluting the 50% plasma in SB17T with AEBSF and EGTA.
Blood samples were collected through submaxillary punctures, and plasma samples were prepared.
Plasma samples were prepared for analysis by extraction in acidified acetonitrile and analyzed by LCECA as previously described [14], [21], [26] [28].
The plasma samples were prepared from heparinised blood samples (between 5 and 10 ml) collected from subjects living in malaria endemic areas of The Gambia between 1991 and 1993, and consist of three groups.
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Study design: A panel of 10 human plasma samples was prepared and spiked with dengue virus types DEN-1 to DEN-4.
In this work, a molecular imprinted polymer (MIP) as a novel selective sorbent for extraction of 3,4-methylenedioxymethamphetamine (MDMA) from plasma samples was prepared.
Protein from plasma samples was prepared in accordance to our previously published methodology [25].
For plasma DH05-1, DH12-3, DH16-1 and DH16-1, two separate experimental plates for each plasma sample were prepared.
Briefly, the plasma sample was prepared for injection onto the column by protein precipitation, followed by centrifugation.
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