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: Recommended - best coverage; Same primer pair as used in probe assay qMmuCEP0059721
PrimePCR™ PreAmp for SYBR® Green Assay: Peg10, Mouse
PrimePCR™ Template for SYBR® Green Assay: Peg10, Mouse
This is a paternally expressed imprinted gene that encodes transcripts containing two overlapping open reading frames (ORFs) RF1 and RF1/RF2 as well as retroviral-like slippage and pseudoknot elements which can induce a -1 nucleotide frame-shift. ORF1 encodes a shorter isoform with a CCHC-type zinc finger motif containing a sequence characteristic of gag proteins of most retroviruses and some retrotransposons. The longer isoform is the result of -1 translational frame-shifting leading to translation of a gag/pol-like protein combining RF1 and RF2. It contains the active-site consensus sequence of the protease domain of pol proteins. Knockout studies in mice suggest that this gene is critical for parthenogenetic development. [provided by RefSeq Feb 2010]
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.