This is the amplicon context sequence in accordance with the minimum information for the publication of real-time quantitative PCR experiements (MIQE) guidelines. For more details, please refer to the following publication, "Primer Sequence Disclosure: A Clarification of the MIQE Guidelines."
Real-time PCR primer assay designed for SYBR® Green gene expression analysis.
Info: Same primer pair as used in probe assay qHsaCEP0040520
PrimePCR™ PreAmp for SYBR® Green Assay: SRA1, Human
PrimePCR™ Template for SYBR® Green Assay: SRA1, Human
Both long non-coding and protein-coding RNAs are transcribed from this gene and they represent alternatively spliced transcript variants. This gene was initially defined as a non-coding RNA which is a coactivator for several nuclear receptors (NRs) and is associated with breast cancer. It has now been found that this gene is involved in the regulation of many NR and non-NR activities including metabolism adipogenesis and chromatin organization. The long non-coding RNA transcripts interact with a variety of proteins including the protein encoded by this gene. The encoded protein acts as a transcriptional repressor by binding to the non-coding RNA. [provided by RefSeq Mar 2012]
Products used to generate validation data:
Amplification of cDNA generated from universal RNA.
Melt curve analysis of above amplification.
Standard curve generated using 20 million copies of template diluted 10 fold to 20 copies.