BODIPY™ 581/591 C11 (Lipid Peroxidation Sensor)
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BODIPY™ 581/591 C11 (Lipid Peroxidation Sensor)
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BODIPY™ 581/591 C11 (Lipid Peroxidation Sensor)

BODIPY™ 581/591 C11 undecanoic acid (Lipid Peroxidation Sensor) is a sensitive fluorescent probe for lipid peroxidation assays that localizes toRead more
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Catalog NumberQuantity
D38611 mg
Catalog number D3861
Price (CNY)
2,195.00
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Ends: 31-Dec-2025
2,954.00
Save 759.00 (26%)
Each
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Quantity:
1 mg
Price (CNY)
2,195.00
Online Exclusive
Ends: 31-Dec-2025
2,954.00
Save 759.00 (26%)
Each
Add to cart

BODIPY™ 581/591 C11 undecanoic acid (Lipid Peroxidation Sensor) is a sensitive fluorescent probe for lipid peroxidation assays that localizes to membranes in live cells. Oxidation of the polyunsaturated butadienyl portion of this fatty acid analog in live cells results in a shift of the fluorescence emission peak from red (∼590 nm) to green (∼510 nm), allowing ratiometric analysis of lipid peroxidation using fluorescence microscopy, high-content analysis, and flow cytometry. In the reduced state, the excitation and emission maxima of BODIPY 581/591 C11 is 581/591 nm; after oxidation, the probe shifts the excitation and emission to 488/510 nm.

Lipid peroxidation is the oxidative degradation of cellular lipids by free radicals from reactive oxygen species, which can degrade lipids containing carbon-carbon double bonds such as phospholipids and polyunsaturated fatty acids. Oxidation of lipids leads to the generation of lipid peroxides and can cause damage to cell membranes, resulting in changes to signal transduction pathways and eventually leading to cell death. Lipid peroxidation is involved in apoptosis and one of the main contributors to ferroptosis, an iron-dependent, non-apoptotic form of cell death. Oxidative stress from lipid peroxidation plays a role in aging, as well as pathologies such as cancer, atherosclerosis, and neurodegenerative diseases.

The BODIPY 581/591 C11 reagent provides a sensitive method to measure lipid peroxidation that occurs in these biological processes and pathological conditions. Because it shifts its fluorescence emission upon oxidation and can be measured through ratiometric fluorescence analysis at two wavelengths, measurement with the BODIPY 581/591 C11 reagent can minimize variations in fluorescence intensity due to factors such as indicator concentration, excitation intensity, and photobleaching. The BODIPY 581/591 C11 reagent can also be used for fluorometric lipid peroxidation assays of antioxidant efficacy in plasma and lipid vesicles.

The BODIPY™ 581/591 C11 (Lipid Peroxidation Sensor) reagent is also available in the Image-iT™ Lipid Peroxidation Kit (Cat. No. C10445) which includes cumene hydroperoxide as a positive control to induce lipid peroxidation in live cells.

We recommend dissolving in high-quality anhydrous DMSO to attain a stock concentration of 1 to 10 mM.

For Research Use Only. Not for use in diagnostic procedures.
Specifications
Quantity1 mg
Detection MethodFluorescence
Excitation/Emission581/591 nm
IndicatorROS
Product LineBODIPY
Product TypeLipid Sensor
Unit SizeEach

Frequently asked questions (FAQs)

What solvent should be used to reconstitute/dissolve BODIPY 581/591 C11 (Lipid Peroxidation Sensor) (Cat. No. D3861)?

For BODIPY 581/591 C11 (Cat No. D3861), we recommend that you dissolve this in dimethyl sulfoxide (DMSO). You can prepare a stock solution in any concentration between 1 and 5 mg/mL. Please note that the BODIPY/DMSO stock solution must be stored at -20 degrees C, desiccated and protected from light.

Find additional tips, troubleshooting help, and resources within our Cell Imaging Support Center.

Citations & References (47)

Citations & References
Abstract
Cell death during ischemia: relationship to mitochondrial depolarization and ROS generation.
Authors:Levraut J, Iwase H, Shao ZH, Vanden Hoek TL, Schumacker PT
Journal:Am J Physiol Heart Circ Physiol
PubMed ID:12388276
Ischemia-reperfusion injury induces cell death, but the responsible mechanisms are not understood. This study examined mitochondrial depolarization and cell death during ischemia and reperfusion. Contracting cardiomyocytes were subjected to 60-min ischemia followed by 3-h reperfusion. Mitochondrial membrane potential (DeltaPsi(m)) was assessed with tetramethylrhodamine methyl ester. During ischemia, DeltaPsi(m) decreased to ... More
Improved efficacy of stem cell labeling for magnetic resonance imaging studies by the use of cationic liposomes.
Authors:van den Bos EJ, Wagner A, Mahrholdt H, Thompson RB, Morimoto Y, Sutton BS, Judd RM, Taylor DA
Journal:Cell Transplant
PubMed ID:14653621
'Labeling stem cells with FDA-approved superparamagnetic iron oxide particles makes it possible to track cells in vivo with magnetic resonance imaging (MRI), but high intracellular levels of iron can cause free radical formation and cytotoxicity. We hypothesized that the use of cationic liposomes would increase labeling efficiency without toxic effects. ... More
Action of DCFH and BODIPY as a probe for radical oxidation in hydrophilic and lipophilic domain.
Authors:Yoshida Y, Shimakawa S, Itoh N, Niki E
Journal:Free Radic Res
PubMed ID:14567446
'Fluorogenic probes such as 2'',7''-dichlorofluorescin (DCFH) have been extensively used to detect oxidative events and to measure antioxidant capacity. At the same time, however, the inherent drawbacks of these probes such as non-specificity towards oxidizing species have been pointed out. The present study was carried out to analyze the action ... More
A method to measure the oxidizability of both the aqueous and lipid compartments of plasma.
Authors:Aldini G, Yeum KJ, Russell RM, Krinsky NI
Journal:Free Radic Biol Med
PubMed ID:11677037
'The lipophilic radical initiator (MeO-AMVN) and the fluorescent probe C11BODIPY581/591 (BODIPY) were used to measure the lipid compartment oxidizability of human plasma. Aqueous plasma oxidizability was initiated by the aqueous peroxyl radical generator, AAPH, and 2'',7''-dichlorodihydrofluorescein (DCFH) was employed as the marker of the oxidative reaction. The distribution in aqueous ... More
Detection of lipid peroxidation in equine spermatozoa based upon the lipophilic fluorescent dye C1l-BODIPY581/591.
Authors:Ball BA, Vo A
Journal:J Androl
PubMed ID:11868820
'The lipophilic fluorescent probe, 4,4-difluoro-5-(4-phenyl-1 ,3-butadienyl)-4-bora-3a,4a-diaza-s-indacene-3-undecanoic acid (C11-BODIPY581/591) was used to evaluate changes in lipid peroxidation in equine spermatozoa during both short-term exposure to ferrous sulfate and sodium ascorbate in the presence of cumene hydroperoxide as well as during storage of spermatozoa at 5 degrees C for 48 hours. Peroxidation ... More