S7701-M
TRAPeze™Telomerase Positive Control Cell Pellet
This product is intended for use with the components of the TRAPEZE Telomerase Detection Kit, the TRAPEZE XL Telomerase Detection Kit & the TRAPEZE ELISA Telomerase Detection Kit.
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About This Item
UNSPSC-Code:
41116012
eCl@ss:
32160405
NACRES:
NA.84
Empfohlene Produkte
Qualitätsniveau
Hersteller/Markenname
Chemicon®
Allgemeine Beschreibung
This product is intended for use with the components of the TRAPEZE™ Telomerase Detection Kit (Catalog # S7700), the TRAPEZE XL Telomerase Detection Kit (Catalog # S7707) and the TRAPEZE ELISA Telomerase Detection Kit (Catalog # S7750). Recommended Taq polymerases: must be non-proofreading, having no exonuclease activity and capable of "hot-start." Titanium Taq, Platinum Taq are suggested.
Material Provided
Each vial of S7701 TRAPEZE Positive Control Cell Pellet contains one million cells, pelletted to the bottom of the microcentrifuge tube.
Material Provided
Each vial of S7701 TRAPEZE Positive Control Cell Pellet contains one million cells, pelletted to the bottom of the microcentrifuge tube.
Anwendung
Instructions for Use
1. Resuspend the cell pellet in 200 μl of 1X CHAPS Lysis Buffer.
2. Incubate the suspension on ice for 30 minutes.
3. Spin the sample in a microcentrifuge at 12,000 X g for 20 minutes at 4°C.
4. Transfer 160 μl of the supernatant into a fresh tube.
5. Aliquot and quick-freeze the remaining extract on dry ice, and store at -75°C to -85°C. The extracts for the TRAP assay should be quick-frozen on dry ice after each use. Aliquots should not be freeze-thawed more than 5 times to avoid loss of telomerase activity. Additionally, aliquoting reduces the risk of contamination.
6. Use 1000 cell equivalents (2 μl of a 1:10 dilution) per TRAP assay, according to the kit manuals.
1. Resuspend the cell pellet in 200 μl of 1X CHAPS Lysis Buffer.
2. Incubate the suspension on ice for 30 minutes.
3. Spin the sample in a microcentrifuge at 12,000 X g for 20 minutes at 4°C.
4. Transfer 160 μl of the supernatant into a fresh tube.
5. Aliquot and quick-freeze the remaining extract on dry ice, and store at -75°C to -85°C. The extracts for the TRAP assay should be quick-frozen on dry ice after each use. Aliquots should not be freeze-thawed more than 5 times to avoid loss of telomerase activity. Additionally, aliquoting reduces the risk of contamination.
6. Use 1000 cell equivalents (2 μl of a 1:10 dilution) per TRAP assay, according to the kit manuals.
Research Category
All
All
This product is intended for use with the components of the TRAPEZE Telomerase Detection Kit, the TRAPEZE XL Telomerase Detection Kit & the TRAPEZE ELISA Telomerase Detection Kit.
Verpackung
1x10(e6) cells
Lagerung und Haltbarkeit
Must be stored at -75°C to -85°C. Telomerase in specimens stored as a cell pellet is stable at this temperature for several years. Once the cell extract is made (in 1X CHAPS Lysis Buffer), it is stable for 1 year, if not subjected to more than 5 freeze-thaw cycles
Rechtliche Hinweise
CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
TRAPEZE is a trademark of Merck KGaA, Darmstadt, Germany
Haftungsausschluss
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
Lagerklassenschlüssel
12 - Non Combustible Liquids
WGK
WGK 2
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Analysenzertifikate (COA)
Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.
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A M Zahler et al.
Nature, 350(6320), 718-720 (1991-04-25)
The ends or telomeres of the linear chromosomes of eukaryotes are composed of tandem repeats of short DNA sequences, one strand being rich in guanine (G strand) and the complementary strand in cytosine. Telomere synthesis involves the addition of telomeric
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