LysoTracker™ amarillo HCK-123, envase especial

Citas y referencias (8)

Invitrogen™

LysoTracker™ amarillo HCK-123, envase especial

HCK-123 LysoTracker™ Yellow es una tinción amarilla fluorescente que tiñe los compartimentos ácidos de las células vivas con unos nivelesMás información

Número de catálogo	Cantidad
L12491	20 x 50 μL

Número de catálogo L12491

Precio (MXN)

Cantidad:

20 x 50 μL

HCK-123 LysoTracker™ Yellow es una tinción amarilla fluorescente que tiñe los compartimentos ácidos de las células vivas con unos niveles máximos de excitación/emisión de ∼465/535 nm.

Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.

Especificaciones

ColorAmarillo

Concentración1 mM

DescripciónLysoTracker™ amarillo HCK-123

Método de detecciónFluorescente

EmisiónAmarillo, amarillo/naranja

Intervalo de longitud de onda de excitación465/535

Para utilizar con (equipo)Microscopio de fluorescencia, generador de imágenes de fluorescencia

FormularioLíquido

Línea de productosLysoTracker

Cantidad20 x 50 μL

Condiciones de envíoTemperatura ambiente

Tipo de etiquetaTinción de orgánulos de células vivas, sin fijación

Tipo de productoTinte

SubCellular LocalizationLisosomas

Unit SizeEach

Contenido y almacenamiento

Almacenar desecado a ≤ –20°C
• Proteger de la luz
• Evitar ciclos de congelación y descongelación y no almacenar en un congelador sin escarcha
• Almacenar en alícuotas de un solo uso, si es posible

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

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