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 efficiency; Same primer pair as used in probe assay qHsaCEP0050290
PrimePCR™ PreAmp for SYBR® Green Assay: MAN2B1, Human
PrimePCR™ Template for SYBR® Green Assay: MAN2B1, Human
This gene encodes an enzyme that hydrolyzes terminal non-reducing alpha-D-mannose residues in alpha-D-mannosides. Its activity is necessary for the catabolism of N-linked carbohydrates released during glycoprotein turnover and it is member of family 38 of glycosyl hydrolases. The full length protein is processed in two steps. First a 49 aa leader sequence is cleaved off and the remainder of the protein is processed into 3 peptides of 70 kDa 42 kDa (D) and 13/15 kDa (E). Next the 70 kDa peptide is further processed into three peptides (A B and C). The A B and C peptides are disulfide-linked. Defects in this gene have been associated with lysosomal alpha-mannosidosis. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq Mar 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.