AAT Bioquest offers a focused selection of fluorescent indicators and assay kits for detecting and quantifying sodium and potassium ions in biological samples. These tools are essential for studying ion homeostasis, membrane transport, and channel function in cellular physiology research. Our SoNa™ indicator dyes provide excellent sodium selectivity over potassium, while our Screen Quest™ platform enables convenient potassium channel screening without wash steps.
Ion Target
Application
Recommended Products
Na⁺
Solution-based quantification
Amplite® Kit, Portelite™ Kit
Na⁺
Cell-based imaging
SoNa™ 520
K⁺
Potassium channel screening
Screen Quest™ Kit
Sodium Ion
SoNa™ 520 Sodium Indicator
SoNa™ 520 is AAT Bioquest's proprietary sodium-sensitive fluorescent indicator that exhibits strong fluorescence enhancement upon sodium binding. With excitation/emission at 491/511 nm, it is compatible with standard FITC filter sets. The indicator demonstrates excellent selectivity for sodium over potassium, making it ideal for accurate sodium measurements in biological samples where both ions are present. In live cell experiments under similar conditions, it has also demonstrated significantly brighter fluorescence responses compared to other sodium indicators such as SBFI.
Key Features
High sodium selectivity — Minimal response to potassium ions ensures accurate sodium-specific detection
Bright green fluorescence — Ex/Em 491/511 nm compatible with standard FITC/GFP filter sets
Cell-permeable AM ester available — SoNa™ 520 AM enables intracellular sodium monitoring in live cells
Large dynamic range — Strong fluorescence intensity increase upon sodium binding
Fig. 1
The fluorescence intensity of SoNa™-520 was measured at 525 nm (excitation at 490 nm) in the presence of Na+ (red) or K+ (blue) ranging from 0.59 to 600 mM in 100 mM Tris buffer (pH=7.5).
Sodium Ion Quantification Kits
For convenient and accurate sodium quantification, AAT Bioquest offers complete assay kits with optimized reagents and standards. These fluorimetric kits utilize our SoNa™ 520 indicator technology and are suitable for microplate reader-based measurements in 96-well or 384-well formats.
Key Features
Amplite® platform — Robust, optimized formulations for reliable quantitative results
Portelite™ format — Portable, ready-to-use kit design for streamlined workflows
High sensitivity — Fluorimetric detection enables low sodium concentration measurements
Excellent selectivity — Minimal interference from potassium and other common ions
Microplate compatible — Suitable for 96-well and 384-well plate formats
The Screen Quest™ No Wash Potassium Channel Assay Kit enables functional screening of potassium channels in cell-based assays. This homogeneous, no-wash format is ideal for high-throughput screening applications in drug discovery, particularly for hERG channel safety screening. The kit detects thallium (Tl⁺) influx through open potassium channels as a functional surrogate for potassium conductance and does not directly measure intracellular potassium concentration.
Key Features
No-wash protocol — Homogeneous assay format reduces handling steps and improves throughput
HTS-compatible — Optimized for 96-well and 384-well microplate formats
hERG screening ready — Validated for cardiac safety screening of potassium channel modulators
Robust signal — Strong fluorescence response enables reliable detection of channel activity
Flexible applications — Compatible with various potassium channel subtypes
Fig. 3
K2SO4 dose dependent hERG channel activity was measured in HEK293-KCNH2 cells with Screen Quest™ Potassium Ion Channel Kit. The cells were seeded overnight at 20,000 cells/100 µL/well in a Costar black wall/clear bottom 96-well poly-D-lysine plate. The cells were incubated with 100 µL of dye-loading solution for 1 hour at 37°C. Final concentration of 1 mM , 0.5 mM, 0.25 mM or 0 mM Tl2SO4 and different concentration of K2SO4 containing stimulus solution was injected in each well by FlexStation and the plate was read every 1-2 sec for 3 minutes at excitation/emission=490/525nm.
This document (01.0240.251203r1) was last updated on Thu Feb 12 2026. All trademarks and registered trademarks mentioned herein are the property of their respective owners.