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1  between these two datasets and with a fixed external standard.
2  analyte in the honey spectra, together with external standards.
3 ed for spectral calibration with internal or external standards.
4  verified by retention times and spikes with external standards.
5 led and (15)N-labeled wild-type ribosomes as external standards.
6 that usually implies using known internal or external standards.
7  a protein-induced bend angle independent of external standards.
8 n of A. fumigatus DNA was achieved by use of external standards.
9 wn, was eliminated after adjustment with the external standards.
10 d unadjusted and adjusted to a common set of external standards.
11  detection. and comparison with internal and external standards.
12 anine for humans, based on the recoveries of external standards.
13 leased in the leachate through multi-element external standards.
14 cation is commonly done against internal and external standards.
15                                        Three external standards (1.5 x 10(3) to 1.5 x 10(6) copies/ml
16 rnal calibrant in addition to routinely used external standards, adjacent brain sections of mice with
17 -inositol (Ins) were quantitated by using an external standard and LCModel, a user-independent quanti
18 eas retinyl palmitate was quantified with an external standard and ultraviolet light detection.
19  separate theory or a calibration against an external standard and without requiring the use of a sol
20 guous multi-sites of DNA methylation without external standards and expensive instrumentation, this P
21 is similar amplification efficiencies of all external standards and samples.
22 tion, cross-validation with multiple sets of external standards, and long-term instrumental stability
23 nts the development of a rapid and sensitive external-standard-based PCR assay for the absolute quant
24     In summary, this report presents a rapid external-standard-based PCR method for the quantificatio
25 reference standard to eliminate the need for external standard calibration and to minimize sample-han
26 on factor of 100, enabling, thus, the use of external standard calibration instead of matrix-matched
27 retreatment of the raw milk sample and using external standard calibration is suitable.
28                                           An external standard calibration method was employed for qu
29 x effect was found, which allowed the use of external standard calibration method.
30             For E2-3,17S, E3-3S, and E2-17S, external standard calibration was used for quantitation,
31            The method evaluation was done by external standard calibration with linearity range betwe
32 ple Quadrupole MS in negative MRM mode using external standard calibration.
33 dard, 2,4,4'-trihydroxydeoxybenzoin, and the external standards daidzein, genistein, and genistin.
34 cation based on internal standards (ISTD) vs external standards (ESTD), single vs multiple ISTD, and
35  This work also describes the preparation of external standards for absolute quantification by NanoSI
36 we estimated recoveries of both internal and external standards in 5 different soyfoods weekly.
37 cision and unambiguous measurements than the external standard method and providing to be a novel and
38  standard was developed and compared with an external standard method, with the internal standard met
39 phate buffer at pH 3 and 40 mM NaPF(6) using external standard method.
40 antitated with uv detection at 204 nm and an external standard method.
41 l methods, verified for efficiency using the external standard method.
42 acellular compartment (Nai) compared with an external standard (monitored by Na-NMR spectroscopy, TmD
43 d for data integration that requires neither external standards nor internal statistics but relies on
44 ter quality to be positively correlated with external standards of cluster quality.
45 ation of cargo loading in LNPs often require external standard preparations and preseparation of unlo
46 2) > 0.99 and RSD < 20%) were obtained using external standards prepared in each control matrix.
47                                              External standards prepared in neat solvents were used f
48 ch combined a limited number of internal and external standards, provided the same 15 ppm mass accura
49 rnal standardization was more efficient than external standard, resulting in a smaller measurement of
50                              Spiking with an external standard RNA controls for all subsequent steps
51  NMR, and BA levels were determined using an external standard solution added to the sample rotor.
52        Three kinds of calibration were used: external standard, standard addition and calibration in
53                     When quantitated with an external standard the use of DPCR in tandem with a PCR a
54 le and easy-to-measure functional outcome or external standard, the confounding effects of concurrent
55 H magnetic resonance spectroscopy (MRS) with external standards to measure absolute brain metabolite
56 efully calibrated and validated internal and external standards to provide such reliability.
57 hermal desorption EI-MS/MS with reference to external standards using a commercially available quadru
58                                  No internal/external standard was used.
59                                           No external standards were necessary.
60 ase chain reaction (PCR) using gene-specific external standards with cDNA from AAAs (n= 19) and norma