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Chunk #30 — Methods — Quantitative real-time PCR.

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Tissue-specific genetic control of splicing: implications for the study of complex traits.
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FAM-labeled β-actin was used as an internal control in a multiplex reaction. Assays were performed according to standard methods (900-nM primer and 250-nM probe in 20-μl reaction mix, Applied Biosystems). Fluorescence outputs were quantified in real time using a 7900HT Fast Real Time PCR System and the data were analyzed using SDS software v.2.2.2 (Applied Biosystems).