LysoTracker™ Green DND-26, special packaging
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LysoTracker™ Green DND-26, special packaging
Invitrogen™

LysoTracker™ Green DND-26, special packaging

LysoTracker Green DND-26 is a cell-permeable, non-fixable, green fluorescent dye that stains acidic compartments within a cell, such as lysosomes.Read more
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Catalog NumberQuantity
L752620 x 50 μL
Catalog number L7526
Price (CNY)
4,383.00
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Ends: 31-Dec-2025
5,941.00
Save 1,558.00 (26%)
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Quantity:
20 x 50 μL
Price (CNY)
4,383.00
Online Exclusive
Ends: 31-Dec-2025
5,941.00
Save 1,558.00 (26%)
Each
Add to cart
LysoTracker Green DND-26 is a cell-permeable, non-fixable, green fluorescent dye that stains acidic compartments within a cell, such as lysosomes. Green DND-26 has an excitation and emission maximum of 504/511 nm and can be efficiently excited using a FITC filter. LysoTracker probes are available in a variety of fluorescent colors.

Simple, highly specific, one-step staining and tracking of acidic organelles
LysoTracker probes consist of a hydrophobic fluorophore linked to a weak base that is only partially protonated at neutral pH. In a neutrally charge state, LysoTracker probes can freely diffuse across intact plasma membranes of live cells. Due to the inherently acidic properties within the lysosome, upon diffusion into the lysosome the weakly basic moiety is protonated. In this charged state, the probe does not readily diffuse across the organelle membrane, providing a localized accumulation for distinct staining of acidic organelles such as lysosomes. Effective at nanomolar concentrations, LysoTracker probes are highly selective for acidic organelles and provide simple one-step staining that does not rely on antibody detection.

Lysosomes are acidic in nature due to the production and storage of digestive enzymes (hydrolases). The acidic environment of lysosomes enables degradation of carbohydrates, lipids, nucleic acids, and peptides. Extracellular proteins, virus or bacteria can also be internalized and trafficked to the lysosome for degradation via the lysosomal proteolysis pathway. In addition, misfolded proteins or damaged organelles become targets for lysosomal degradation via the induction of autophagy. Autophagy is important for cellular differentiation, survival during nutrient deprivation, and normal growth control. The inherent acidic nature within lysosomes, and any change of pH during biosynthesis or pathogenesis, can be exploited by various probes that respond to an acidic environment. LysoTracker products provide fluorescence detection for live-cell staining of acidic environments and can be used for labeling and tracing acidic organelles such as lysosomes.



Visualize staining your cell without wasting your reagents, antibodies, or time with our new Stain-iT Cell Staining Simulator.

For Research Use Only. Not for use in diagnostic procedures.
Specifications
ColorGreen
Concentration1 mM
DescriptionLysoTracker™ Green DND-26
Detection MethodFluorescence
EmissionGreen
Excitation Wavelength Range504/511
For Use With (Equipment)Fluorescence Microscope, Fluorescent Imager
Product LineLysoTracker
Quantity20 x 50 μL
Shipping ConditionRoom Temperature
Label TypeFluorescent Dye
Product TypeDye
SubCellular LocalizationLysosomes
Unit SizeEach
Contents & Storage
Store desiccated at ≤–20°C
• Protect from light
• Avoid freeze-thaw cycles and do not store in a frost-free freezer
• Store in single-use aliquots, if possible

Frequently asked questions (FAQs)

What is the recommended incubation time for LysoTracker Green DND-26 (Cat. No. L7526) and LysoSensor Yellow/Blue DND-160 (Cat. No. L7545)?

LysoTracker Green DND-26 (Cat. No. L7526) and LysoSensor Yellow/Blue DND-160 (Cat. No. L7545) show faster uptake in cells and consequently a faster "alkalizing effect" on the lysosomes, so we recommend incubating the cells with these probes for 1-5 min at 37 degrees C. As the other LysoTracker and LysoSensor probes have a slower rate of uptake, we recommend a longer incubation time of 30 min to 2 hr.

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

Citations & References (102)

Citations & References
Abstract
Biocompatibility, endocytosis, and intracellular trafficking of mesoporous silica and polystyrene nanoparticles in ovarian cancer cells: effects of size and surface charge groups.
Authors:Ekkapongpisit M, Giovia A, Follo C, Caputo G, Isidoro C,
Journal:Int J Nanomedicine
PubMed ID:22904626
Nanoparticles engineered to carry both a chemotherapeutic drug and a sensitive imaging probe are valid tools for early detection of cancer cells and to monitor the cytotoxic effects of anticancer treatment simultaneously. Here we report on the effect of size (10-30 nm versus 50 nm), type of material (mesoporous silica ... More
Induction of autophagy and cell death by tamoxifen in cultured retinal pigment epithelial and photoreceptor cells.
Authors:Cho KS, Yoon YH, Choi JA, Lee SJ, Koh JY,
Journal:Invest Ophthalmol Vis Sci
PubMed ID:22786900
We investigated the mechanism of tamoxifen (TAM) retinotoxicity using human retinal pigment epithelial (RPE)-derived (ARPE-19) and photoreceptor-derived (661W) cells. Cultured ARPE-19 and 661W cells were treated with 5 to 10 µM TAM, and the resultant cell death was quantified using lactate dehydrogenase (LDH) release assay. Cellular oxidative stress was determined ... More
Regulation of endocytosis via the oxygen-sensing pathway.
Authors:Wang Y, Roche O, Yan MS, Finak G, Evans AJ, Metcalf JL, Hast BE, Hanna SC, Wondergem B, Furge KA, Irwin MS, Kim WY, Teh BT, Grinstein S, Park M, Marsden PA, Ohh M,
Journal:Nat Med
PubMed ID:19252501
'Tumor hypoxia is associated with disease progression, resistance to conventional cancer therapies and poor prognosis. Hypoxia, by largely unknown mechanisms, leads to deregulated accumulation of and signaling via receptor tyrosine kinases (RTKs) that are critical for driving oncogenesis. Here, we show that hypoxia or loss of von Hippel-Lindau protein--the principal ... More
Quantitative measurement of mast cell degranulation using a novel flow cytometric annexin-V binding assay.
Authors:Demo SD, Masuda E, Rossi AB, Throndset BT, Gerard AL, Chan EH, Armstrong RJ, Fox BP, Lorens JB, Payan DG, Scheller RH, Fisher JM
Journal:Cytometry
PubMed ID:10404150
'BACKGROUND: Mast cells are primary mediators of allergic inflammation. Antigen-mediated crosslinking of their cell surface immunoglobulin E (IgE) receptors results in degranulation and the release of proinflammatory mediators including histamine, tumor necrosis factor-alpha, and leukotrienes. METHODS: Mast cells were stimulated to degranulate by using either IgE crosslinking or ionophore treatment. ... More
Inhibition of the vacuolar H(+)-pump with bafilomycin A1 does not induce acrosome reaction or activate proacrosin in mouse spermatozoa.
Authors:Codelia VA, Cortes CJ, Moreno RD
Journal:Biochem Biophys Res Commun
PubMed ID:16236270
'Acrosomal protease activation is regarded as an important event triggered by acrosomal reaction and leading to sperm passage through zona pellucida. Mammalian acrosome has an internal acid pH that probably helps to maintain inactive proenzymes that otherwise could be precociously activated and prevent normal fertilization. In this work, we have ... More