Flow cytometry is a methodology that allows performing simultaneous multi-parametric analysis of single cells in solution. Flow cytometers utilize lasers as light sources to produce both scattered and fluorescent light signals. Cell populations can be characterized and/or purified based on their fluorescent or light scattering characteristics.
Protein expression on cell surface and intracellular molecules can be detected using appropriate fluorescent probes. This technology can be also applied in medium-throughput screening to study the interaction of compounds for a target of interest, for instance by competition binding.
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CELT- 174 hD2 Dopamine receptor fluorescent antagonist (589/616)
Our potent hD2 dopamine receptor fluorescent antagonist is available in a 10ug vial, allowing you to prepare 73ml of 100nM working solution to test D2R.
432,00€
Our CELT-174 product has been specifically designed to meet the needs of researchers in a variety of fields, enabling the study of D2 dopamine receptors with greater accuracy and precisionView moreOur potent and selective hD2 Dopamine receptor fluorescent antagonist shows high affinity for hD2 receptor and selectivity over the other receptor subtypes (Ki =1.06 nM for hD2 receptor in radioligand binding assay). It allows to perform cell visualization in fluorescence microscopy, confocal microscopy and high content system experiments. It is potentially suitable for other fluorescence-based assays.
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CELT- 426 hD2 Dopamine receptor fluorescent antagonist (560/571)
Our CELT-426 product is available in a 10ug vial that allows you to prepare 67ml of 100nM working solution to test D2R.
432,00€
It has been specifically designed for high potency and selectivity, demonstrating a high affinity for D2 receptors and may be suitable for fluorescence-based assaysView moreOur potent and partially selective hD2 Dopamine receptor fluorescent antagonist shows high affinity for hD2 receptor and partial selectivity over the other receptor subtypes (Ki =89.3 nM for hD2 receptor in radioligand binding assay). It has been validated in Fluorescence Polarization binding assays as a valid alternative to radioligand binding assays.It allows to perform cell visualization in fluorescence microscopy, confocal microscopy and high content system experiments. It is potentially suitable for other fluorescence-based assays.
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CELT-240 hD2/D3 Dopamine receptors fluorescent ligand (589/616)
Our CELT-240 product is available in a 10ug vial that allows you to prepare 78ml of 100nM working solution to test D2R/D3R.
432,00€
It demonstrates high potency and selectivity, making it a valuable tool for researchers interested in studying the D2 and D3 receptorsView moreOur potent hD3/D2 Dopamine receptors fluorescent ligand shows high affinity for hD2 and hD3 receptors (Ki =2.34 nM and 2.14 nM respectively in radioligand binding assays) and selectivity over D4 dopamine receptor. It allows to perform cell visualization in fluorescence microscopy, confocal microscopy and high content system experiments. It is potentially suitable for other fluorescence-based assays.
Do you want more information?
If you want to know more about how to use fluorescent ligands to characterize receptors with pharmacological interest with this and other technologies, click on the button to download the article “Fluorescent ligands: A new method to label your GPCRs”