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 qHsaCEP0049818
PrimePCR™ PreAmp for SYBR® Green Assay: ACHE, Human
PrimePCR™ Template for SYBR® Green Assay: ACHE, Human
Acetylcholinesterase hydrolyzes the neurotransmitter acetylcholine at neuromuscular junctions and brain cholinergic synapses and thus terminates signal transmission. It is also found on the red blood cell membranes where it constitutes the Yt blood group antigen. Acetylcholinesterase exists in multiple molecular forms which possess similar catalytic properties but differ in their oligomeric assembly and mode of cell attachment to the cell surface. It is encoded by the single ACHE gene and the structural diversity in the gene products arises from alternative mRNA splicing and post-translational associations of catalytic and structural subunits. The major form of acetylcholinesterase found in brain muscle and other tissues is the hydrophilic species which forms disulfide-linked oligomers with collagenous or lipid-containing structural subunits. The other alternatively spliced form expressed primarily in the erythroid tissues differs at the C-terminal end and contains a cleavable hydrophobic peptide with a GPI-anchor site. It associates with the membranes through the phosphoinositide (PI) moieties added post-translationally. [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.