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The model has been validated using age-specific results from six IPTi trials with SP [53].
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Furthermore, more than thirty putative Inc proteins have now been validated using specific antibodies, mostly in C. trachomatis (Table 1).
The age-specific abundance pattern for fibrinogen determined using the 2D-DIGE was validated using a fibrinogen specific antibody (Figure 3).
The real-time PCR was validated using the specific instructions from OIE [35].
The amplification of the 11q13 region was validated using locus-specific FISH.
In addition, gain of 7p12 and amplification of 11q13 were validated using locus-specific BAC clones RP11-339F13 and RP11-300I6, respectively.
This segregation was validated using species-specific signatures and in-silico restriction enzyme analysis.
These results were validated using chromosome specific EST and SSR markers and GISH analysis.
Such calculations should be validated using specific bypass flow measurements.
This assay was validated using an shRNA specific for the GFP sequence (shR-E19) which consistently showed 80% silencing efficiency.
Results were validated using an independent expression array platform, together with specific Taqman qRT-PCR assays.
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