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Home MicroRNA 3' UTR Clones

PHKA2 (NM_000292) 3β-UTR clone in pMirTarget

| Specifications |
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| Cat. No. |
Description |
Price |
Availability |
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| SC213033 |
3`UTR clone of phosphorylase kinase alpha 2 (liver) (PHKA2) for miRNA target validation |
$495.00 |
4 weeks * |
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* Delivery time is an estimate in business days. Occasional delays may occur due to unforeseen complexities in the preparation of your construct. International customers may expect an additional 1-2 weeks in shipping
Also for PHKA2 (NM_000292)
OriGene TrueClone Data
| Vector: | pMirTarget |
Insert Size: 1211 |
Restriction Site: SgfI-MluI |
| Sequence Data: | Insert Sequence |
| OTI Disclaimer: | Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs). |
| Product Components: | The cDNA clone is shipped in a 2-D bar-coded Matrix tube as 10 ug dried plasmid DNA. The package also includes 100 pmols of both the corresponding 5' and 3' vector primers in separate vials. |
Reference Data
| RefSeq: | NM_000292.2 |
| Synonyms : | GSD9A; PHK; PYK; PYKL; XLG; XLG2 |
| Locus ID: | 5256 |
| Summary: | Phosphorylase kinase is a polymer of 16 subunits, four each of alpha, beta, gamma and delta. The alpha subunit includes the skeletal muscle and hepatic isoforms, and the hepatic isoform is encoded by this gene. The beta subunit is the same in both the muscle and hepatic isoforms, and encoded by one gene. The gamma subunit also includes the skeletal muscle and hepatic isoforms, which are encoded by two different genes. The delta subunit is a calmodulin and can be encoded by three different genes. The gamma subunits contain the active site of the enzyme, whereas the alpha and beta subunits have regulatory functions controlled by phosphorylation. The delta subunit mediates the dependence of the enzyme on calcium concentration. Mutations in this gene cause glycogen storage disease type 9A, also known as X-linked liver glycogenosis. Alternatively spliced transcript variants have been reported, but the full-length nature of these variants has not been determined.[provided by RefSeq, Feb 2010]. |
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