LysoTracker™ Yellow HCK-123, special packaging
LysoTracker™ Yellow HCK-123, special packaging
Invitrogen™

LysoTracker™ Yellow HCK-123, special packaging

LysoTracker Yellow HCK-123 is a cell-permeable, non-fixable, yellow fluorescent dye that stains acidic compartments within a cell, such as lysosomes.YellowRead more
Catalog NumberQuantity
L1249120 x 50 μL
Catalog number L12491
Price (JPY)
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Ends: 27-Mar-2026
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20 x 50 μL
LysoTracker Yellow HCK-123 is a cell-permeable, non-fixable, yellow fluorescent dye that stains acidic compartments within a cell, such as lysosomes.Yellow HCK-123 has an excitation and emission maximum of 465/535 nm. 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.


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For Research Use Only. Not for use in diagnostic procedures.
Specifications
ColorYellow
Concentration1 mM
DescriptionLysoTracker™ Yellow HCK-123
Detection MethodFluorescence
EmissionYellow, Yellow/Orange
Excitation Wavelength Range465/535
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 (8)

Citations & References
Abstract
Insect lipoprotein follows a transferrin-like recycling pathway that is mediated by the insect LDL receptor homologue.
Authors:Van Hoof D, Rodenburg KW, Van der Horst DJ
Journal:J Cell Sci
PubMed ID:12356906
'The lipoprotein of insects, high-density lipophorin (HDLp), is homologous to that of mammalian low-density lipoprotein (LDL) with respect to its apolipoprotein structure. Moreover, an endocytic receptor for HDLp has been identified (insect lipophorin receptor, iLR) that is homologus to the LDL receptor. We transfected LDL-receptor-expressing CHO cells with iLR cDNA ... More
Distinct pathways of antigen uptake and intracellular routing in CD4 and CD8 T cell activation.
Authors:Burgdorf S, Kautz A, Böhnert V, Knolle PA, Kurts C
Journal:Science
PubMed ID:17463291
The mechanisms that allow antigen-presenting cells (APCs) to selectively present extracellular antigen to CD8+ effector T cells (cross-presentation) or to CD4+ T helper cells are not fully resolved. We demonstrated that APCs use distinct endocytosis mechanisms to simultaneously introduce soluble antigen into separate intracellular compartments, which were dedicated to presentation ... More
Cholesterol level regulates endosome motility via Rab proteins.
Authors:Chen H, Yang J, Low PS, Cheng JX,
Journal:Biophys J
PubMed ID:17981910
The role of cholesterol in the regulation of endosome motility was investigated by monitoring the intracellular trafficking of endocytosed folate receptors (FRs) labeled with fluorescent folate conjugates. Real-time fluorescence imaging of HeLa cells transfected with green fluorescent protein-tubulin revealed that FR-containing endosomes migrate along microtubules. Moreover, microinjection with antibodies that ... More
Dynamics and mechanisms of quantum dot nanoparticle cellular uptake.
Authors:Xiao Y, Forry SP, Gao X, Holbrook RD, Telford WG, Tona A,
Journal:J Nanobiotechnology
PubMed ID:20550705
ABSTRACT: BACKGROUND: The rapid growth of the nanotechnology industry and the wide application of various nanomaterials have raised concerns over their impact on the environment and human health. Yet little is known about the mechanism of cellular uptake and cytotoxicity of nanoparticles. An array of nanomaterials has recently been introduced ... More
Plasma membrane associated location of sulfonated meso-tetraphenylporphyrins of different hydrophilicity probed by total internal reflection fluorescence spectroscopy.
Authors:Sailer R, Strauss WS, Emmert H, Stock K, Steiner R, Schneckenburger H
Journal:Photochem Photobiol
PubMed ID:10824598
Sulfonated meso-tetraphenylporphyrins of different hydrophilicity were microspectrofluorimetrically examined in endothelial cells using total internal reflection (TIR) illumination or epi-illumination. Since the penetration depth of the evanescent field during TIR illumination is limited to a few hundred nanometers, photosensitizers were almost selectively examined in close vicinity to the plasma membrane. Pronounced ... More