LysoTracker™ Red DND-99, special packaging
LysoTracker™ Red DND-99, special packaging
Invitrogen™

LysoTracker™ Red DND-99, special packaging

LysoTracker Red DND-99 is a cell-permeable red fluorescent dye that stains acidic compartments within a cell, such as lysosomes. RedRead more
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Catalog NumberQuantity
L752820 x 50 μL
Catalog number L7528
Price (HKD)
4,128.00
Each
Add to cart
Quantity:
20 x 50 μL
Price (HKD)
4,128.00
Each
Add to cart
LysoTracker Red DND-99 is a cell-permeable red fluorescent dye that stains acidic compartments within a cell, such as lysosomes. Red DND-99 has an excitation and emission maximum of 577/590 nm and can be efficiently excited using a TRITC filter. LysoTracker probes are available in a variety of fluorescent colors. Although it does not crosslink with cells, LysoTracker Red DND-99 shows transient retention after methanol-free formaldehyde fixation for a short period of time.

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
ColorRed
Concentration1 mM
DescriptionLysoTracker™ Red DND-99
Detection MethodFluorescence
EmissionVisible Red
Excitation Wavelength Range577/590
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

Citations & References (237)

Citations & References
Abstract
Testosterone signaling through internalizable surface receptors in androgen receptor-free macrophages.
Authors:Benten WP,Lieberherr M,Stamm O,Wrehlke C,Guo Z,Wunderlich F
Journal:Molecular biology of the cell
PubMed ID:10512854
Testosterone acts on cells through intracellular transcription-regulating androgen receptors (ARs). Here, we show that mouse IC-21 macrophages lack the classical AR yet exhibit specific nongenomic responses to testosterone. These manifest themselves as testosterone-induced rapid increase in intracellular free [Ca(2+)], which is due to release of Ca(2+) from intracellular Ca(2+) stores. ... More
Authors:
Journal:
PubMed ID:9030618
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
Streptococcal serum opacity factor increases the rate of hepatocyte uptake of human plasma high-density lipoprotein cholesterol.
Authors:Gillard BK, Rosales C, Pillai BK, Lin HY, Courtney HS, Pownall HJ,
Journal:Biochemistry
PubMed ID:20879789
Serum opacity factor (SOF), a virulence determinant of Streptococcus pyogenes, converts plasma high-density lipoproteins (HDL) to three distinct species: lipid-free apolipoprotein (apo) A-I, neo HDL, a small discoidal HDL-like particle, and a large cholesteryl ester-rich microemulsion (CERM) that contains the cholesterol esters (CE) of up to ~400000 HDL particles and ... More