logo
AAT Bioquest

ER-Lite™ Blue-White DPX *Cell-Permeable*

Product key features

  • Selective ER Targeting - Specifically labels the endoplasmic reticulum with minimal off-target staining, outperforming conventional ER dyes like DiOC₆(3).
  • High Photostability and Brightness - Features a high extinction coefficient and quantum yield, delivering bright and stable fluorescence ideal for extended imaging sessions.
  • Large Stokes Shift and Broad Emission - Emits across 430–640 nm with a large Stokes shift, compatible with standard DAPI or UV long-pass filter sets.
  • Environment-Sensitive Fluorescence - Responds to changes in solvent polarity with emission shifts and quantum yield variations, enabling dynamic studies of ER conditions.
  • Live-Cell and Two-Photon Imaging Compatible - Cell-permeant and non-cytotoxic at working concentrations; supports two-photon microscopy for high-resolution, deep-tissue imaging.

Product description

ER-Lite™ Blue-White DPX is a highly photostable, environment-sensitive fluorescent probe designed for selective imaging of the endoplasmic reticulum (ER) in live cells. As a member of the Dapoxyl™ (DPX) dye family, it exhibits a large Stokes shift, high extinction coefficient, and exceptional quantum yield, making it an optimal tool for fluorescence microscopy. With an excitation maximum at approximately 374 nm, ER-Lite™ Blue-White DPX emits across a broad spectral range (430–640 nm), facilitating visualization using standard DAPI or UV long-pass optical filters.

This probe demonstrates superior selectivity for the ER, with minimal off-target labeling of mitochondria, unlike conventional ER stains such as DiOC₆(3). Its cell-permeant nature enables efficient intracellular uptake, and it remains non-cytotoxic at low working concentrations. The fluorescence properties of ER-Lite™ Blue-White DPX are highly environment-sensitive, shifting to longer emission wavelengths as solvent polarity increases while exhibiting a concomitant decrease in quantum yield. These characteristics allow for the study of ER organization and dynamics under various physiological conditions.

ER-Lite™ Blue-White DPX is also compatible with two-photon microscopy, expanding its applicability for high-resolution, deep-tissue imaging. While aldehyde fixation partially retains staining patterns, significant fluorescence signal loss should be anticipated. When used according to the optimized staining protocol, ER-Lite™ Blue-White DPX enables high-contrast, high-fidelity visualization of the ER, making it a valuable tool for investigating ER structure, function, and its involvement in cellular homeostasis and stress responses.

Spectrum

Page updated on April 15, 2025

Ordering information

Price
Unit size
Catalog Number22626
Quantity
Add to cart

Additional ordering information

Telephone1-800-990-8053
Fax1-800-609-2943
Emailsales@aatbio.com
InternationalSee distributors
Bulk requestInquire
Custom sizeInquire
Technical SupportContact us
Purchase orderSend to sales@aatbio.com
ShippingStandard overnight for United States, inquire for international
Request quotation

Physical properties

Molecular weight

580.53

Solvent

DMSO

Spectral properties

Excitation (nm)

372

Emission (nm)

548

Storage, safety and handling

H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22

Storage

Freeze (< -15 °C); Minimize light exposure
UNSPSC12171501
HeLa cells were seeded overnight and incubated with 1 µM ER-Lite™ Blue-White DPX Cell-Permeable Dye for 30 minutes at 37°C in a 5% CO₂ atmosphere. Following incubation, cells were washed with HH Buffer and imaged using a DAPI long-pass (DAPI-LP) filter set. Subsequently, the cells were counterstained with Nuclear Green LCS1 (#17540) according to the standard protocol and imaged using a GFP filter set (pseudo-colored red). Image overlays were generated using Keyence Analysis Software.
HeLa cells were seeded overnight and incubated with 1 µM ER-Lite™ Blue-White DPX Cell-Permeable Dye for 30 minutes at 37°C in a 5% CO₂ atmosphere. Following incubation, cells were washed with HH Buffer and imaged using a DAPI long-pass (DAPI-LP) filter set. Subsequently, the cells were counterstained with Nuclear Green LCS1 (#17540) according to the standard protocol and imaged using a GFP filter set (pseudo-colored red). Image overlays were generated using Keyence Analysis Software.
HeLa cells were seeded overnight and incubated with 1 µM ER-Lite™ Blue-White DPX Cell-Permeable Dye for 30 minutes at 37°C in a 5% CO₂ atmosphere. Following incubation, cells were washed with HH Buffer and imaged using a DAPI long-pass (DAPI-LP) filter set. Subsequently, the cells were counterstained with Nuclear Green LCS1 (#17540) according to the standard protocol and imaged using a GFP filter set (pseudo-colored red). Image overlays were generated using Keyence Analysis Software.