|
|
Home MicroRNA 3' UTR Clones

RASA1 (NM_002890) 3β-UTR clone in pMirTarget

| Specifications |
Related Products |
Product Manual |
FAQs |
| Cat. No. |
Description |
Price |
Availability |
|
| SC212043 |
3`UTR clone of RAS p21 protein activator (GTPase activating protein) 1 (RASA1) transcript variant 1 for miRNA target validation |
$495.00 |
4 weeks * |
 |
* 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 RASA1 (NM_002890)
OriGene TrueClone Data
| Vector: | pMirTarget |
Insert Size: 1051 |
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_002890.1 |
| Synonyms : | CM-AVM; CMAVM; GAP; p120GAP; p120RASGAP; PKWS; RASA; RASGAP |
| Locus ID: | 5921 |
| Summary: | The protein encoded by this gene is located in the cytoplasm and is part of the GAP1 family of GTPase-activating proteins. The gene product stimulates the GTPase activity of normal RAS p21 but not its oncogenic counterpart. Acting as a suppressor of RAS function, the protein enhances the weak intrinsic GTPase activity of RAS proteins resulting in the inactive GDP-bound form of RAS, thereby allowing control of cellular proliferation and differentiation. Mutations leading to changes in the binding sites of either protein are associated with basal cell carcinomas. Mutations also have been associated with hereditary capillary malformations (CM) with or without arteriovenous malformations (AVM) and Parkes Weber syndrome. Alternative splicing results in two isoforms where the shorter isoform, lacking the N-terminal hydrophobic region but retaining the same activity, appears to be abundantly expressed in placental but not adult tissues. [provided by RefSeq, May 2012]. |
|