TR-FRET Bridge-It SAM 384
1332.6 EUR
In Stock
quantity
Produktdetaljer
Katalognummer: 10136 - TRF-1-1-1004B
Produktkategori: Företag och industri > Vetenskap och laboratorium
Gentaur
Storlek: 1 Kit
Parameters
| Storage and shipping | Store all at -20ºC until use |
|---|
TRF-1-1-1003A
TR-FRETBridge-It®SAM50
10 mM S-adenosyl methionine standard in 10mM 2-mercaptoethanol, SAM Assay Solution, Buffer S, Buffer CM
7985 €
TRF-1-1-1003B
TR-FRETBridge-It®SAM96
10 mM S-adenosyl methionine standard in 10mM 2-mercaptoethanol, SAM Assay Solution, Buffer S, Buffer CM
14411 €
TRF-1-1-1004A
TR-FRETBridge-It®SAM100
10 mM S-adenosyl methionine standard in 10mM 2-mercaptoethanol, SAM Assay Solution, Buffer S, Buffer CM
6378.5 €
60709
PDE10A1 TR-FRET Assay Kit
The PDE10A1 TR-FRET Assay Kit is designed for identification of inhibitors of PDE10A1 using TR-FRET (Time Resolved Fluorescence Resonance Energy Transfer) technology. Using this kit, only two simple steps on a microtiter plate are required for the PDE10A1 activity assay. First, the fluorescent-labeled cAMP is incubated with a sample containing PDE10A1 for 1 hour. Second, a binding agent and a terbium donor are added to the reaction mix and incubated for 1 hour. Then, fluorescence intensity can be measured using a fluorescence reader._x000D_
757.5 €
60710
PDE10A2 TR-FRET Assay Kit
The PDE10A2 TR-FRET Assay Kit is designed for identification of inhibitors of PDE10A2 using TR-FRET (Time Resolved Fluorescence Resonance Energy Transfer) technology. Using this kit, only two simple steps on a microtiter plate are required for the PDE10A2 activity assay. First, the fluorescent-labeled cAMP is incubated with a sample containing PDE10A2 for 1 hour. Second, a binding agent and a terbium donor are added to the reaction mix and incubated for 1 hour. Then, fluorescence intensity can be measured using a fluorescence reader.
757.5 €
40342
SMARCA2 TR-FRET Assay Kit
The SMARCA2 TR-FRET Assay Kit is designed to measure the inhibition of SMARCA2 (BRM) binding to its substrate in a homogeneous 384 reaction format. This FRET-based assay requires no time-consuming washing steps, making it especially suitable for high throughput screening applications. The assay procedure is straightforward and simple; a sample containing terbium-labeled donor, dye-labeled acceptor, SMARCA2, substrate, and an inhibitor is incubated for 120 minutes. Then, the fluorescence intensity is measured using a fluorescence reader.
975 €
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