Cell membrane orange red fluorescent probe(Dil) , CAS No.C598349

CAS: C598349 Cat. No.: C598349 Molecular Weight: 933.9
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Storage
Store at 2-8°C,Protected from light
Shipped In
Wet ice
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Size
Status
Price
Qty
200μl
C598349-200μl
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

$205.90

$240.90
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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.

Overview

Product introduction:

Cytombritetm cell membrane orange red fluorescent probe (DII) is a lipophilic carbocyanine dye, which can effectively and stably label the plasma membrane and intracellular membrane structures. It has the characteristics of low cytotoxicity and will not transfer between cells. It is often used as a tracer molecule for cell fusion, adhesion and migration. Compared with PKH dyes, cytombrite dyes are convenient to use and evenly colored. DiI (orange fluorescence), DIO (green fluorescence), did (red fluorescence) and other cell membrane fluorescent dyes, such as dir (near-infrared fluorescence) and nir680 (far-infrared dye), provide effective tools for multicolor imaging and flow cytometry analysis. Cytombrite series dyes can also be used for the staining of cells after formaldehyde fixation, and are compatible with the formaldehyde fixation step after staining. This series of dyes is not suitable for bacteria or yeast. At 100 per use μ L dyeing working solution calculation, 200 μ L stock solution can be used for 400 times.

Product parameters:

Ex/em (MeOH) = 549/565 nm molecular formula: c59h97cln2o4 molecular weight: 933.9

Matters needing attention:

1. before use, centrifuge the product to the bottom of the tube in time, and then conduct subsequent tests. 2. fluorescent dyes have quenching problems. Please try to avoid light to slow down fluorescence quenching. 3. for your safety and health, please wear experimental clothes and disposable gloves.

Scope of application:

Cell membrane dye

Product Features:
Low toxicity: It has low cytotoxicity and will not transfer between cells;
Good stability: strong fluorescence brightness, uniform coloring, and suitable for cell tracking, which can work well inside cells The reservation;
Strong compatibility: Dyeing can be performed before and after formaldehyde fixation.
Spectral diagram: 

Bring your own materials:

1. Consumables
(1) Centrifuge tube (2) cover glass
2. Reagents
(1) Serum free medium or HBSS or PBS (2) medium (pre warmed)
3. Instruments
Fluorescence microscope or flow cytometer

Operating steps:

It is recommended to optimize the volume of working fluid according to different cell lines and experimental systems. Suggest starting to explore the optimal conditions within the range of 1010 times the recommended quantity.
1. Suspension cell staining
(1) Add an appropriate volume of culture medium to resuspend the cells to a density of 1 × 106/mL, and then add the staining solution in a ratio of 1:200.
(2) Incubate cells at 37 ℃ for 2-20 minutes, and the optimal culture time varies for different cells. A starting incubation time of 20 minutes can be used to optimize the system afterwards.
(3) Centrifuge at 1000~1500 rpm for 5 minutes. Pour the supernatant and slowly add the culture medium preheated at 37 ℃ again to resuspend the cells. Repeat twice.
2. Staining of adherent cells
(1) Preparation of staining solution: Add 5 μ L of staining solution to every 1 mL of culture medium, vortex and mix well.
(2) Cultivate the adherent cells on sterile cover glass, remove the cover glass after cultivation, absorb excess culture medium, but keep the surface moist.
(3) Add 100 μ L of staining solution to one corner of the cover glass and gently shake to evenly cover all cells with the dye.
(4) Incubate cells at 37 ℃ for 2-20 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 achieve uniform labeling effect.
(5) Absorb 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 absorb the culture medium. But keep the surface moist.
3. Result detection
The sample can be detected in the culture medium and analyzed by fluorescence microscopy imaging or flow cytometry.
Note: Yellow light excitation, Cy3 filter can be selected as the fluorescence microscope filter; Select YL1 channel for flow cytometry.

Specifications

Storage
Store at 2-8°C, Protected from light
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers
Molecular Weight 933.9

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

Certificates(CoA,COO,BSE/TSE and Analysis Chart)
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.

2 results found

Lot NumberCertificate TypeDateItem
F2603375Certificate of AnalysisApr 16, 2026 C598349
I2518720Certificate of AnalysisSep 12, 2025 C598349
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