DXB-NIR
DXB-NIR is a push-pull dioxaboron fluorescent probe with solvatochromic properties, featuring high fluorescence brightness, photostability, and a large two-photon absorption cross-section. DXB-NIR exhibits Ex/Em of 550/620–780 nm (with two-photon excitation at 930 nm). DXB-NIR quantifies local polarity via the intensity ratio I (>640)/I (<640) between the far-red channel (<640 nm) and the near-infrared channel (>640 nm), and it can simultaneously label the plasma membrane, endoplasmic reticulum, and lipid droplets in live cells. DXB-NIR monitors the increase in local polarity of various cell compartments under conditions of cholesterol depletion, starvation, and oxidative stress. DXB-NIR can be used for polarity imaging of biological membranes and lipid droplets, as well as studies related to cellular stress.
For research use only. We do not sell to patients.
- CAS No.: 2477607-64-8
- Formula: C28H29BF2N2O5
- Molecular Weight:522.35
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Description
In Vitro
Guidelines (The following is a recommended experimental protocol for guidance only, and adjustments are required based on your specific needs)
1. Stock Solution Preparation
1.1 Solvent: For most dyes, organic solvents such as anhydrous DMSO are commonly used for dissolution.
1.2 Concentration Recommendation: Prepare a high-concentration stock solution at 1-10 mM.
2. Working Solution Preparation
2.1 Diluent: Serum-free medium or PBS is typically used. Proteins and esterases in serum may interfere with staining results or cause dye hydrolysis.
2.2 Working Concentration: 100-200 nM.
2.3 Notes: Adjust the working solution concentration as needed; prepare fresh before use.
3. Staining Procedure
3.1 Sample Type Description
3.1.1 Adherent cells[1][2]: HeLa cells and A549 cells.
3.2 Incubation Conditions
3.2.1 Incubate with DXB-NIR in OptiMEM at 20°C for 30 min.
3.3 Washing
5. Detection and Analysis
5.1 Instrument Type: Fluorescence microscope (spinning disk confocal, wide-field, two-photon or laser confocal microscope).
5.2 Excitation/Emission Wavelengths
5.2.1 Single-photon imaging: Excitation wavelength is 550 nm; emitted light is split into a far-red channel (<640 nm) and a near-infrared (NIR) channel (>640 nm).
5.2.2 Two-photon imaging: Excitation wavelength is 930 nm; emitted light is split into a far-red channel (<640 nm) and a near-infrared (NIR) channel (>640 nm).
5.3 Result Analysis
5.3.1 Changes in fluorescence intensity: Under stress conditions (cholesterol depletion, starvation, oxidative stress), increased intensity in the near-infrared (NIR) channel (>640 nm) indicates enhanced local polarity of lipid compartments; fluorescence changes corresponding to polarity changes of lipid droplets under nutrient deficiency and oxidative stress conditions can be detected.
5.3.2 Fluorescence localization: Localizes to the plasma membrane, endoplasmic reticulum and lipid droplets in live cells.
5.3.3 Color changes: Shows far-red color (<640 nm, pseudocolored green) in low-polarity environments (such as liquid-ordered membrane phases, plasma membrane); shows near-infrared color (>640 nm, pseudocolored red) in high-polarity environments (such as liquid-disordered membrane phases, stressed lipid compartments).
5.3.4 Ratio analysis: Calculate the intensity ratio of the near-infrared (NIR) channel to the far-red channel (I (>640)/I (<640)) to quantify polarity differences among different cellular compartments and under different stress conditions.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 2477607-64-8
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Molecular Weight 522.35
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Formula C28H29BF2N2O5
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SMILES
CCN(C1=CC=C2C(OC(C3=C2OB(F)(O=C3/C=C/C4=CC5=C(O4)C=C(C=C5)N(CC)CC)F)=O)=C1)CC
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)