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 qHsaCIP0030735
PrimePCR™ PreAmp for SYBR® Green Assay: SHPK, Human
PrimePCR™ Template for SYBR® Green Assay: SHPK, Human
The protein encoded by this gene has weak homology to several carbohydrate kinases a class of proteins involved in the phosphorylation of sugars as they enter a cell inhibiting return across the cell membrane. Sequence variation between this novel gene and known carbohydrate kinases suggests the possibility of a different substrate cofactor or changes in kinetic properties distinguishing it from other carbohydrate kinases. The gene resides in a region commonly deleted in cystinosis patients suggesting a role as a modifier for the cystinosis phenotype. The genomic region is also rich in Alu repetitive sequences frequently involved in chromosomal rearrangements. [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.