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pHSense Eu Monomeric Streptavidin, 96 Assay Points

The pHSense™ Eu Monomeric Streptavidin involves a Europium-labeled, pH-sensitive streptavidin that allows real-time, no-wash detection of biotinylated ligand and binder internalization, and intracellular trafficking in live-cell assays.

Feature Specification
Application Internalization

The pHSense™ Eu Monomeric Streptavidin involves a Europium-labeled, pH-sensitive streptavidin that allows real-time, no-wash detection of biotinylated ligand and binder internalization, and intracellular trafficking in live-cell assays.

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Unit Size: 96 Assay Points
Part #:
81SAMEU1AA
List price
USD 599.00
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Unit Size: 2 x 96 Assay Points
Part #:
81SAMEU1AB
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USD 1,098.00
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Unit Size: 10 x 96 Assay Points
Part #:
81SAMEU1AC
List price
USD 3,872.00
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For research use only. Not for use in diagnostic procedures. All products to be used in accordance with applicable laws and regulations including without limitation, consumption and disposal requirements under European REACH regulations (EC 1907/2006).

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Overview

The pHSense Eu Monomeric Streptavidin reagent is non cell permeant and labeled with a pH-sensitive Europium complex. Its monomeric format ensures high-affinity binding to biotinylated ligands while minimizing aggregation, making it ideal for monitoring receptor internalization in live cells. The sequence contains an N-terminal 6His-tag and a C-terminal FLAG-tag.

At neutral extracellular pH (≥7), its fluorescence remains minimal. Once internalized, the pHSense Eu Monomeric Streptavidin encounters increasingly acidic compartments such as early and late endosomes and lysosomes, where the Europium signal becomes progressively stronger. This novel pH sensitive Europium complex is compatible with a time-resolved fluorescence (TRF) detection, effectively eliminating most fluorescence background and significantly enhancing the signal-to-background ratio. Its unique photophysical properties enable simple and robust no-wash detection of receptor-mediated endocytosis of binders in plate-based assays with live cells.

How it works

pHSense™ Eu Monomeric SA: internalization assay principle

The pHSense™ Eu monomeric Streptavidin reagent is a monomeric streptavidin that is covalently labeled with a Europium-based pHSense probe. It is designed to monitor the internalization of biotinylated binders in real time.

It ensures high-affinity binding to biotinylated ligands while minimizing aggregation and remains minimally fluorescent at neutral extracellular pH (≥7). Upon internalization, the monomeric streptavidin-binder complex encounters increasingly acidic intracellular compartments, including early and late endosomes and lysosomes, where the pHSense probe generates a fluorescent signal that becomes progressively stronger and longer-lived.

pHSense™ Eu Monomeric SA: internalization assay principle
pHSense generic graph

Assay protocol for monitoring binder internalization

The assay begins with culturing cells in a 96-well plate. The biotinylated test binder is pre-incubated with pHSense™ Eu Monomeric SA reagents at a 1:2 molar ratio in cell culture medium or pHSense BSA Internalization Buffer 1X (Part #: 81BUFBR1, Revvity) for 30 minutes at room temperature. The resulting complex is then added to the cells and incubated at 37°C, followed by kinetic or endpoint fluorescence measurement using a TRF-compatible plate reader.

Note: A protocol for monitoring internalization in suspension cell lines is also available. Please refer to the user’s manual for details.

Assay protocol for monitoring binder internalization

Assay protocol for monitoring binder-induced receptor and membrane protein internalization

The assay begins with culturing cells in a 96-well plate. The biotinylated binder directed against the target of interest is pre-incubated with pHSense™ Eu Monomeric SA at a 1:2 molar ratio in cell culture medium or pHSense BSA Internalization Buffer 1X (Part #: 81BUFBR1, Revvity) for 30 minutes at room temperature.

The mixture is then added to the cells and incubated for 1 hour at room temperature. Following the incubation, cells are stimulated with a pharmacological compound.

The fluorescent signal is measured with a TRF-compatible plate reader. Readings are done repeatedly at several time-points for a kinetic study or after appropriate incubation times for endpoint assays.

Assay protocol for monitoring receptor and membrane protein-mediated internalization

Assay validation

Internalization of anti-HER2 antibody Trastuzumab

BT-474 cells were seeded in a 96-well white culture-treated plate at a density of 20,000 cells/well in complete culture medium, and incubated overnight at 37°C and 5% CO₂.

Biotinylated Trastuzumab (an anti-HER2 internalizing antibody) was pre-incubated at room temperature for 30 minutes with pHSense™ Eu Monomeric SA at a 1:2 molar ratio in cell-culture medium. The Monomeric SA-antibody mixture was then serially diluted in cell-culture medium and 50 µL of each dilution was added to the cells, followed by a 20-hour incubation at 37°C, 5% CO₂.

The fluorescent signal was recorded on an EnVision™ Nexus Multimode Microplate Reader (Part# HH36000002, Revvity).

The resulting dose-dependent signal increase shows pHSense™ Eu Monomeric SA reagents specifically detect the internalization of the anti-HER2 antibody.

pHSense-based monitoring of anti-HER2 internalizing antibody

Specifications

Application
Internalization
Automation Compatible
Yes
Brand
pHSense
Detection Modality
pH sensitive dye
Product Group
Fluorescent Reagent
Shipping Conditions
Shipped in Dry Ice
Target
Biotin
Target Class
ADCs
Antibodies
Cell surface proteins
Cell surface proteins, antibodies, ADCs
GPCRs
Technology
TRF
Unit Size
96 Assay Points

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