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The both samples are analysed separately to reduce the heterogeneity.
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Both samples were analysed for pH as described by Mckeague (1978) total nitrogen using Kjeldahl procedure followed by distillation described by Bremner and Mulvaney (1982); Organic carbon using the method described by Walkley (1947); Available phosphorus and extractable cations such as Ca2+, Mg2+ and Fe2+ by atomic absorption spectrophotometer.
The asymptotic response functions, derived through Monte-Carlo simulations for polycrystalline Pb and ZrH2 samples, are analysed in both DD and SD methods, and compared with the experimental ones for Pb sample.
First, athletes' urine and blood samples are analysed according to the current list of prohibited doping substances and methods.
The carbon content in both the samples is analysed by proximity analysis and elemental analysis by EDS (energy dispersive spectroscopy technique)[2].
In parallel, aliquots of mobile phase were spiked with the same amount of sweeteners' mixture, and both types of samples were analysed by HPLC/MS.
When both sets of samples were analysed together, the results showed that the combination of 3 genes (ACTB, UBB and B2M) is sufficient for adequate normalisation).
Initially, both the RD and LD samples were analysed, as shown in Fig. 3, to confirm the percentage of Al present as well as its elemental composition.
Both tumoural and normal samples were analysed.
Both native and spiked samples were analysed in five replicates.
Both fresh and dried mango samples were analysed for moisture content (MC), pH and ascorbic acid.
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