Sentence examples for measured transcript from inspiring English sources

First, to independently validate and to quantitate the expression levels of sigmar in larval salivary glands prior to and during developmental cell death, we employed quantitative reverse transcription PCR (QRT-PCR) and measured transcript levels in wild-type OreR salivary glands (16, 20 and 23 hours APF at 18°C; equivalent to 8.5, 11 and 12.5 hours APF at 25°C).

To elucidate the roles of SNB and OsIDS1 in controlling flowering time, we measured transcript levels of the previously identified floral regulators in OX plants.

Among others, the group measured transcript profiles of 77 differentially expressed genes in primary human endothelial cells in vitro after external irradiation of 2 Gy with a 137Cs source, demonstrating that the maximum differential expression (>1.5-fold change) occurred between 8 and 12 days after irradiation.

Next, we measured transcript levels of the enzymes involved in glutamine metabolism.

Here, we measured transcript levels of control transfected or HIF-1α-targeted pulmonary epithelia.

The measured transcript abundance was normalized to the level of POLR2A (RNA Polymerase II) for all samples.

To assess if the accumulation of rpl2 transcripts was reversible, we measured transcript levels during and after two heat treatment sessions (Fig. 4).

Thus, we measured transcript levels of CD73 [62], VEGF [63], Fibronectin1 (FN1) [64] and COX2 [65] after 24 h of RSV infection of A549 pulmonary epithelial cells using different RSV infection doses (MOI1-5).

With increasing distance of the primary tag from the 5' end of the gene, there was a decrease in the MPSS-measured transcript abundance.

Immunohistochemical protein staining in ADM muscle correlated MxA staining with the microarray-measured transcript levels, which are pronounced in the ADM samples but not those of other inflammatory muscle disease samples (IBM, PM, dystrophies and necrotizing myositis).

Methods that apply microarray profiling would – by using the available and measured transcript-specific probes – provide additional information not on the expression levels of a gene but also the respective splice isoforms.