Seleccione un Tamaño
| Talla/SKU | Disponibilidad | Precio |
|---|
Acerca de este artículo
General description
The TRAPEZE™ XL Kit is a highly sensitive in vitro assay for the fluorometric detection of telomerase activity. It incorporates refinements to the original TRAP assay that were first introduced in the gel-based TRAPEZE™ Telomerase Detection Kit (Cat #S7700). As in the original TRAPEZE™ Kit, primer sequence modifications that reduce amplification artifacts and an internal PCR control are included. In addition, the TRAPEZE™ XL Kit uses fluorescence energy transfer (ET) primers to generate fluorescently labeled TRAP products which permit nonisotopic, quantitative analysis of telomerase activity.
The unique design of these ET primers (Amplifluor® primers) allows detection and quantification of telomerase activity by directly measuring fluorescence emission in the reaction vessels. Since Amplifluor® primers will fluoresce only upon incorporation into the TRAP products or the internal control, post-PCR sample manipulations such as electrophoretic gel or ELISA analyses are eliminated, thereby reducing the the risk of carry-over contamination. Quantitative analysis is not compromised when detection is performed in a high-throughput 96-well format unlike platforms utilizing a qualitative ELISA. In addition, inclusion of an internal control labeled with a second fluorophore serves to both monitor PCR amplification and aid in the quantitation of telomerase activity.
Telomerase is a ribonucleoprotein that synthesizes and directs the telomeric repeats onto the 3′ end of existing telomeres using its RNA component as a template (10-14). Telomerase activity has been shown to be specifically expressed in immortal cells, cancer and germ cells (15,16) where it compensates for telomere shortening during DNA replication and thus stabilizes telomere length (7,17). These observations have led to a hypothesis that telomere length may function as a "mitotic clock" to sense the number of cell divisions and eventually signal replicative senescence or programmed cell death when a critical telomere length is achieved. Therefore, expression of telomerase activity in cancer cells may be a necessary and essential step for tumor development and progression (16,18-20). The causal relationship between expression of telomerase and telomere length stabilization and the extension of the life span of the human cell has recently been reported (21).
Recommended Taq polymerases: must be non-proofreading, having no exonuclease activity and capable of "hot-start." Titanium Taq, Platinum Taq are suggested.
Preparation Note
Other Notes
Legal Information
Disclaimer
1 of 1
Este artículo | |||
|---|---|---|---|
| description - | description A highly sensitive in vitro assay for the fluorometric detection & real time quantification of telomerase activity in cells. | description 1X CHAPS Lysis Buffer is a component of the gel-and ELISA-based TRAPeze Telomerase Detection Kits & is used in the extraction step of the procedure. | description sufficient for ≤50 reactions, kit of 1 (15 components), suitable for cell culture |
| technique(s) PCR: suitable | technique(s) - | technique(s) - | technique(s) cell culture | mammalian: suitable |
| Quality Level 100 | Quality Level 100 | Quality Level 100 | Quality Level - |
| species reactivity mammals | species reactivity - | species reactivity - | species reactivity - |
| application(s) genomic analysis | application(s) genomic analysis | application(s) - | application(s) - |
telomere length detection PCR kit TRAPeze XL | - | - | - |
Still not finding the right product?
Explore all of our products under TRAPeze™ XL Telomerase Detection Kit
Palabra de advertencia
Warning
Códigos de peligro
Indicaciones de precaución
Hazard Classifications
Met. Corr. 1
WGK
WGK 3
Punto de inflamación (°F)
Not applicable
Punto de inflamación (°C)
Not applicable
Clase de almacenamiento
10 - Combustible liquids
Elija entre una de las versiones más recientes:
¿Ya tiene este producto?
Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.



