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Home MicroRNA 3' UTR Clones

BRCA1 (NM_007294) 3β-UTR clone in pMirTarget

| Specifications |
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| Cat. No. |
Description |
Price |
Availability |
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| SC214395 |
3`UTR clone of breast cancer 1 early onset (BRCA1) transcript variant 1 for miRNA target validation |
$495.00 |
1 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 BRCA1 (NM_007294)
OriGene TrueClone Data
| Vector: | pMirTarget |
Insert Size: 1426 |
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_007294.3 |
| Synonyms : | BRCAI; BRCC1; BROVCA1; IRIS; PNCA4; PPP1R53; PSCP; RNF53 |
| Locus ID: | 672 |
| Summary: | This gene encodes a nuclear phosphoprotein that plays a role in maintaining genomic stability, and it also acts as a tumor suppressor. The encoded protein combines with other tumor suppressors, DNA damage sensors, and signal transducers to form a large multi-subunit protein complex known as the BRCA1-associated genome surveillance complex (BASC). This gene product associates with RNA polymerase II, and through the C-terminal domain, also interacts with histone deacetylase complexes. This protein thus plays a role in transcription, DNA repair of double-stranded breaks, and recombination. Mutations in this gene are responsible for approximately 40% of inherited breast cancers and more than 80% of inherited breast and ovarian cancers. Alternative splicing plays a role in modulating the subcellular localization and physiological function of this gene. Many alternatively spliced transcript variants, some of which are disease-associated mutations, have been described for this gene, but the full-length natures of only some of these variants has been described. A related pseudogene, which is also located on chromosome 17, has been identified. [provided by RefSeq, May 2009]. |
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