LysoTracker™ Blue DND-22, special packaging
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LysoTracker™ Blue DND-22, special packaging
Invitrogen™

LysoTracker™ Blue DND-22, special packaging

LysoTracker Blue DND-22 is a cell-permeable, non-fixable, blue fluorescent dye that stains acidic compartments within live cells, such as lysosomes.Read more
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Catalog NumberQuantity
L752520 x 50 μL
Catalog number L7525
Price (CNY)
4,402.00
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Ends: 31-Dec-2025
5,966.00
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Quantity:
20 x 50 μL
Price (CNY)
4,402.00
Online Exclusive
Ends: 31-Dec-2025
5,966.00
Save 1,564.00 (26%)
Each
Add to cart
LysoTracker Blue DND-22 is a cell-permeable, non-fixable, blue fluorescent dye that stains acidic compartments within live cells, such as lysosomes. Blue DND-22 has an excitation and emission maximum of 373/422 nm and can be efficiently excited using a DAPI 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
ColorBlue
Concentration1 mM
DescriptionLysoTracker™ Blue DND-22
Detection MethodFluorescence
EmissionBlue
Excitation Wavelength Range373/422
For Use With (Equipment)Fluorescence Microscope, Fluorescent Imager
FormLiquid
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

Citations & References (26)

Citations & References
Abstract
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
Determination of intracellular organelles implicated in daunorubicin cytoplasmic sequestration in multidrug-resistant MCF-7 cells using fluorescence microscopy image analysis.
Authors:Bour-Dill C, Gramain MP, Merlin JL, Marchal S, Guillemin F
Journal:Cytometry
PubMed ID:10655559
'BACKGROUND: Anthracycline resistance is known to be mediated by P-glycoprotein (P-gp) or multidrug-resistance related protein (MRP) as well as intracellular sequestration of drugs. METHODS: The resistance phenotype of doxorubicin-selected MCF-7(DXR) human breast adenocarcinoma cell line was characterized by cellular and nuclear daunorubicin efflux, P-gp and MRP expression and apoptosis induction. ... More
In situ assessment of cell viability.
Authors:Yang H, Acker J, Chen A, McGann L
Journal:Cell Transplant
PubMed ID:9786064
'Cryobiological studies of tissues often require the simultaneous assessment of tissue structure and in situ cellular function. Localization of damage during cryopreservation occurs as a consequence of tissue structure and morphology and as a result of biophysical constraints imposed by diffusion and heat transfer. This study used five experimental model ... More
Higher order Rab programming in phagolysosome biogenesis.
Authors:Roberts EA, Chua J, Kyei GB, Deretic V
Journal:J Cell Biol
PubMed ID:16982798
'Phagosomes offer kinetically and morphologically tractable organelles to dissect the control of phagolysosome biogenesis by Rab GTPases. Model phagosomes harboring latex beads undergo a coordinated Rab5-Rab7 exchange, which is akin to the process of endosomal Rab conversion, the control mechanisms of which are unknown. In the process of blocking phagosomal ... More
In vitro and in vivo photocytotoxicity of boron dipyrromethene derivatives for photodynamic therapy.
Authors:Lim SH, Thivierge C, Nowak-Sliwinska P, Han J, van den Bergh H, Wagnières G, Burgess K, Lee HB,
Journal:J Med Chem
PubMed ID:20199028
To understand the effects of substitution patterns on photosensitizing the ability of boron dipyrromethene (BODIPY), two structural variations that either investigate the effectiveness of various iodinated derivatives to maximize the  ... More