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1 ffects on the method by thiocyanate, a known interfering substance.
2 ectropolymerized PoPD was used to reduce the interfering substances.
3 nificant change in the presence of different interfering substances.
4 agulants, specimen handling, and potentially interfering substances.
5 ns, BSA was able to override the presence of interfering substances.
6 nal stability and selectivity against common interfering substances.
7 tation procedure for simultaneous removal of interfering substances and concentration of dilute sampl
8 lded inconsistent results, likely because of interfering substances and other peroxidases present in
9 e forming a hydrazone that is separated from interfering substances and quantified by high-performanc
10 -referenced coating scheme that accounts for interfering substances and the enzymatic breakdown produ
11 ecognized malathion in the presence of other interfering substances and thus, can be applied to real
12 producibility and selectivity in presence of interfering substances and was validated with real sampl
13 s devoid of the optical and other endogenous interfering substances derived from lysates of xenograft
14 ern blot analysis and is not affected by the interfering substances found in serum that often affect
16 purification of this enzyme, indicating that interfering substances in crude lysates were not respons
21 f 288 specimens containing various potential interfering substances, nonspecifically reacting substan
23 specimens and plasma containing potentially interfering substances or other blood-borne pathogens.
24 his end, serum peptides must be enriched and interfering substances removed: a step that should be au
25 tose as well, this epimer is not a potential interfering substance since its concentration in blood i
26 GLU, while being poorly influenced by common interfering substances such as ascorbate, dopamine and d
27 of a panel of 95 specimens with potentially interfering substances, such as clinically relevant bact
28 e with the addition of 17 different types of interfering substances typically found in the biological
29 roxide oxidation, with exclusion of the main interfering substances uric acid and hydrogen peroxide.
30 asure of conjugation efficiencies because an interfering substance was apparently released by Ig-lp p
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