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 qHsaCIP0031816
PrimePCR™ PreAmp for SYBR® Green Assay: BAI1, Human
PrimePCR™ Template for SYBR® Green Assay: BAI1, Human
Angiogenesis is controlled by a local balance between stimulators and inhibitors of new vessel growth and is suppressed under normal physiologic conditions. Angiogenesis has been shown to be essential for growth and metastasis of solid tumors. In order to obtain blood supply for their growth tumor cells are potently angiogenic and attract new vessels as results of increased secretion of inducers and decreased production of endogenous negative regulators. BAI1 contains at least one 'functional' p53-binding site within an intron and its expression has been shown to be induced by wildtype p53. There are two other brain-specific angiogenesis inhibitor genes designated BAI2 and BAI3 which along with BAI1 have similar tissue specificities and structures however only BAI1 is transcriptionally regulated by p53. BAI1 is postulated to be a member of the secretin receptor family an inhibitor of angiogenesis and a growth suppressor of glioblastomas [provided by RefSeq Jul 2008]
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.