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 qHsaCEP0053892
PrimePCR™ PreAmp for SYBR® Green Assay: NPR1, Human
PrimePCR™ Template for SYBR® Green Assay: NPR1, Human
Guanylyl cyclases catalyzing the production of cGMP from GTP are classified as soluble and membrane forms (Garbers and Lowe 1994 [PubMed 7982997]). The membrane guanylyl cyclases often termed guanylyl cyclases A through F form a family of cell-surface receptors with a similar topographic structure: an extracellular ligand-binding domain a single membrane-spanning domain and an intracellular region that contains a protein kinase-like domain and a cyclase catalytic domain. GC-A and GC-B function as receptors for natriuretic peptides; they are also referred to as atrial natriuretic peptide receptor A (NPR1) and type B (NPR2; MIM 108961). Also see NPR3 (MIM 108962) which encodes a protein with only the ligand-binding transmembrane and 37-amino acid cytoplasmic domains. NPR1 is a membrane-bound guanylate cyclase that serves as the receptor for both atrial and brain natriuretic peptides (ANP (MIM 108780) and BNP (MIM 600295) respectively).[supplied by OMIM May 2009]
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.