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The first set of samples analysed was 100 assumed salmonella-negative pooled samples consisting of faeces originating from 265 different Swedish farms.
A reagent blank and an internal laboratory QC subsample of homogenised butter from a sample that has been analysed many times, was included with each set of samples analysed.
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These percentages are surprisingly good if we consider that we have been comparing data available from two independent sets of samples analysed with two procedures, and the experiments were not originally designed to perform this comparison.
There appears to be no association between HPV type and geographical setting, type of samples analysed or type of primer used to analyse samples in such cancers.
However, there was no clear evidence of an association between geographical setting, type of samples analysed or type of primer, and HPV type in such malignancies.
There were no statistically significant associations between the HPV types analysed and the geographical setting, type of sample analysed or type of primer used to analyse samples in head and neck cancers.
This set of samples was analysed using the developed TFC-LC-MS/MS method.
To determine if freezing the samples and storing them at −40°C affected the levels of IGF-1 and IGF-2, a separate set of samples was analysed.
Four sets of pooled samples were prepared for hybridization to separate Affymetrix rat genome 230 2.0 arrays (i.e. four separate sets of samples were analysed for each condition, prepared from a total of 12 myocyte preparations).
One of the two sets of samples was analysed in PSH using the same techniques applied in the prevalence study.
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).
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