To validate the transcriptional pattern identified by microarray analysis, expression of 42 differentially expressed genes was analyzed using RT-PCR.
In the tumor analysis, expression of Noxa was seen in all biopsies.
The proposed architecture allows these techniques to be integrated with almost any facial analysis expression software available with minimal changes.
Fig. 4 Real-time PCR analysis expression of the eight genes before and after interaction with epithelial cells.
However, the analysis expression of such (p^{ast}) in Theorem 3 may not be the optimal result.
The measurement and the model are generally linked through the approaches of analysis, expression, validation, and prediction.
Using RT-PCR analysis, expression of AcFREP1 and AcFREP2 was shown to be developmentally and tissue-specific and no constitutive expression in haemocytes was found.
In this paper we have studied the equivalence relationship between (l_{2,0} -minimization and (l_{2,0} -minimization, and we have given an anal_{2,p} -minimizationuch (p^{ast}).
In the third experiment, using reverse transcription polymerase chain reaction (RT-PCR) analysis, expression of thyroid hormone receptor (TRα and TRβ0), mRNA was detected in all of the ovarian compartments.
For analysis, expression levels of the housekeeping gene rp49 were used as an RNA loading control.
To validate the micro-array analysis, expression of ZF14 and WRKY53 were monitored by qRT-PCR.
