Sentence examples for quantification normalized from inspiring English sources

Western blotting also showed that the Cx-43 quantification normalized by GAPDH in the collagen group was significantly lower than that in the 0.1 and 0.05 mg/ml CNH-Col groups (**P < 0.01).

A relative quantification normalized against unit mass (50 ng of total RNA) was used to analyze the expression data with the equation: ({text{Ratio}},left( {{{{text{test}}} mathord{left/ {vphantom {{{text{test}}} {{text{calibrator}}}}} right. kern-nulldelimiterspace} {{text{calibrator}}}}} right) = 2^{Delta {text{CT}}} ), as suggested in Real-Time Applications Guide from Bio-Rad.

NC was slightly scattered in the cytoplasm, and perinuclear region western blotting also showed comparable results, such that the NC quantification normalized by GAPDH in the 0.1 mg/ml CNH-Col group was significantly higher than that in the 0.05 mg/ml CNH-Col and collagen groups (***P < 0.001).

(B) Gamma-H2AX signal quantification normalized to GAPDH following a 2 Gy high-LET irradiation.

Quantification normalized histone PTM relative abundances from the mass spectrometry data.

(B) Gamma-H2AX signal quantification normalized to GAPDH following a 2 Gy low-LET irradiation.

Absolute quantification eliminates the need for such post-run data processing, in that absolute quantification normalizes assay-specific differences, such that quantities expressed as the number of target molecules become independent of assay implementation.

Quantification was normalized to the endogenous control H2az.

Quantification was normalized against the number of RPLPO transcripts in the same RNA extracts.

Quantification was normalized for HM-1 mES cells and revealed Utf1 expression levels of around 50% in O9 iPS cells.

Mature miR-145 levels were quantified using TaqMan® MicroRNA Assay (4373133, Applied Biosystems) Quantification was normalized to the U6 small nuclear B non-coding RNA (RNU6B) which served as an endogenous control (4373381, Applied Biosystems).