Dilinoleyl DiI (cell membrane orange red fluorescent probe) , CAS No.D598345

CAS: D598345 Cat. No.: D598345 Peso molecular: 925.80
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Storage
Store at 2-8°C,Protected from light
Shipped In
Wet ice
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Estado
Price
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1mg
D598345-1mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

282,90US$

331,90US$
Guardar 49,00 US$ (14.76%)
5mg
D598345-5mg
1

987,90US$

1.160,90US$
Guardar 173,00 US$ (14.90%)
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Why this grade

for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at 2-8°C,Protected from light Ships Wet ice Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Dilinoleyl DiI, also known as fast DiI, has the same absorption and emission wavelength as DiI. Because dlinoleyl DiI contains unsaturated hydrocarbon chains, the lateral diffusion speed of dilinoleyl DiI on the cell membrane is faster than that of DiI. Because of this property, it is widely used in tracking neuronal tissues. After dilinoleyl DiI staining, paraformaldehyde (methanol and other reagents cannot be used) can be fixed, but permeabilization after staining is not recommended. In addition, after fixed permeabilization (permeabilization with 0.1% TritonX-100 at room temperature), the plasma membrane staining can also be well performed. At 100 per use μ L of dyeing working solution with a concentration of 10 μ According to m calculation, 5 mg of working solution can be used for 5400 times.

Product parameters:

Ex/Em (MeOH) = 549/565 nm

Matters needing attention:

1. please centrifuge the product to the bottom of the tube immediately before use, and then conduct subsequent experiments. 2. when dilinoleyl DiI is used to stain fixed cells or tissue samples, 4% paraformaldehyde prepared in PBS is usually used for fixation. The use of other inappropriate fixatives will lead to high fluorescence background. 3. fluorescent dyes have quenching problems. Please try to avoid light to slow down fluorescence quenching. 4. for your safety and health, please wear experimental clothes and disposable gloves.

Scope of application:

Cell membrane fluorescent dye ; anterograde and retrograde tracing of neurons ; long-term cell tracing

Usage:
1. Preparation of staining solution
(1) Preparation of storage solution: The storage solution is prepared with anhydrous DMSO or EtOH, with a concentration of 1-10 mM.
Note: Unused storage liquids should be packaged and stored at -20 ℃ to avoid repeated freeze-thaw cycles.
(2) Preparation of working solution: Dilute the storage solution with a suitable buffer (such as serum-free medium, HBSS or PBS) and prepare a concentration of 1-10 μ M's working fluid.
Note: It is recommended to optimize the final concentration of the working solution based on different cell lines and experimental systems. It is recommended to start exploring the optimal concentration within a range of 10 times the recommended concentration.
2. Suspension cell staining
(1) Add an appropriate volume of staining solution and resuspend the cells to a density of 1 × 106/mL.
(2) Incubate cells at 37 ℃ for 5-20 minutes, and the optimal culture time varies for different cells. 20 minutes can be used as the starting incubation time, and then the system can be optimized to obtain a uniform labeling effect.
(3) After incubation, centrifuge at 1000-1500 rpm for 5 minutes. Pour the supernatant and slowly add the growth culture medium preheated at 37 ℃ again to resuspend the cells.
(4) Repeat step (3) more than twice.
3. Staining of adherent cells
(1) Cultivate adherent cells on sterile cover slips.
(2) Remove the cover glass from the culture medium and absorb excess culture medium, but keep the surface moist.
(3) Add 100 to one corner of the cover glass μ Gently shake the dye working solution of L to evenly cover all cells with the dye.
(4) Incubate cells at 37 ℃ for 5-20 minutes, and the optimal culture time varies for different cells. 20 minutes can be used as the starting incubation time, and then the system can be optimized to obtain a uniform labeling effect.
(5) Dry the dye working solution, wash the cover glass with culture medium 2-3 times, cover all cells with preheated culture medium each time, incubate for 5-10 minutes, and then dry the culture medium. But keep the surface moist.
4. Result detection
The sample can be detected in the culture medium and analyzed by fluorescence microscopy imaging or flow cytometry.

Specifications

Condiciones de almacenamiento de almacenamiento
Store at 2-8°C, Protected from light
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores
Peso molecular 925.80

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

4 results found

Lot NumberCertificate TypeFechaArticulo
L2522368Certificate of AnalysisDec 16, 2025 D598345
L2502301Certificate of AnalysisNov 25, 2025 D598345
B2426279Certificate of AnalysisJan 16, 2024 D598345
B2426280Certificate of AnalysisJan 16, 2024 D598345
Propiedades químicas y físicas
Solubilidadsoluble in ethanol,DMSO,DMF
Preguntas frecuentes y artículos
Calculadoras de soluciones
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