BAPTA- Oregon Green™ 488, AM, con permeabilidad celular - Embalaje especial
BAPTA- Oregon Green™ 488, AM, con permeabilidad celular - Embalaje especial
Invitrogen™

BAPTA- Oregon Green™ 488, AM, con permeabilidad celular - Embalaje especial

Los indicadores de calcio marcados son moléculas que presentan un aumento de la fluorescencia al unirse a Ca2+. Se puedenMás información
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Número de catálogoCantidad
O680710 x 50 μg
Número de catálogo O6807
Precio (CLP)
506.931
Each
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Cantidad:
10 x 50 μg
Precio (CLP)
506.931
Each
Añadir al carro de la compra
Los indicadores de calcio marcados son moléculas que presentan un aumento de la fluorescencia al unirse a Ca2+. Se pueden utilizar en muchas investigaciones de señalización del calcio, incluida la medición de Ca2+ intracelular, tras la entrada y liberación de Ca2+ y la adquisición de imágenes de excitación multifotónica de Ca 2+ en tejidos vivos. Las células se pueden cargar como éster AM de estos indicadores calcio mediante la adición del indicador disuelto directamente a las placas que contienen las células cultivadas. La señal de fluorescencia de estas células se mide generalmente mediante microscopía de fluorescencia, ensayos de microplacas de fluorescencia o citometría de flujo.

Obtenga más información acerca de los indicadores de iones, incluidos los indicadores de calcio, potasio, pH y potencial de la membrana ›

Indicador de calcio (éster AM) Especificaciones:
• Etiqueta (Ex/Em): Oregon Green™ 488 BAPTA-1 (494/523 nm)
• Aumento de la intensidad de fluorescencia al unirse con Ca2+: ∼14 veces
• Presentan un aumento de la fluorescencia al unirse a Ca2+ con poco cambio en la longitud de onda


Características espectrales de indicadores de calcio Molecular Probes™
Estas sondas se excitan con luz visible y dado que la energía requerida para la excitación es baja, el potencial de fotodaño celular se reduce. Los instrumentos basados en láser de uso habitual (por ejemplo, microscopios de escaneo láser confocal) son capaces de excitar eficientemente esos indicadores, y sus emisiones están en regiones del espectro donde los fondos de dispersión y autofluorescencia celular no suelen causar problemas.

Más opciones para indicadores de calcio fluorescentes
Ofrecemos una gran selección de indicadores de calcio Molecular Probes™ para su uso en diversos escenarios experimentales, por ejemplo, versiones de dextrano para reducir las fugas y la compartimentación, y conjugados BAPTA para detectar perturbaciones transitorias de calcio de gran amplitud. Para obtener más información, consulte Fluorescent Ca2+ Indicators Excited with Visible Light—Section 19.3 (Indicadores de Ca2+ fluorescentes excitados mediante luz visible, sección 19.3) en el manual de Molecular Probes™.

Para obtener información sobre indicadores de Ca2+ excitables mediante UV, indicadores de Ca2+ basados en proteínas, conjugados de indicadores de Ca2+ e indicadores basados en fluorescencia de otros iones metálicos (es decir, Mg2+, Zn2+) consulte Indicators for Ca2+, Mg2+, Zn2+ and Other Metal Ions—Chapter 19 (Indicadores para Ca2+, Mg2+, Zn2+ y otros iones metálicos, capítulo 19) en el manual de Molecular Probes™.

Para uso exclusivo en investigación. No apto para uso diagnóstico o terapéutico en animales o humanos.
Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.
Especificaciones
Método de detecciónFluorescente
Tipo de coloranteA base de colorantes fluorescentes
Cantidad10 x 50 μg
Condiciones de envíoTemperatura ambiente
Para utilizar con (aplicación)Viabilidad y proliferación celulares
Para utilizar con (equipo)Microscopio de fluorescencia, Citómetro de flujo, Lector de microplacas
Línea de productosOregon Green
Tipo de productoTinción
Unit SizeEach
Contenido y almacenamiento
Almacenar en congelador entre -5 °C y -30 °C

Preguntas frecuentes

What cellular processes can be analyzed with a flow cytometer?

-Calcium flux: Each of the Oregon Green calcium indicators binds intracellular calcium with increasing affinity, providing a sensitivity range to match many applications. Oregon Green probes emit green fluorescence at resting levels of Ca2+ and increase their fluorescence intensity 14-fold with increasing Ca2+ concentration. The cell-permeant formulation (Cat. No. O6807) can be loaded in cell media and is compatible with flow cytometry.
-Rhodamine-based calcium indicators comprise a range of probes for large or small changes in Ca2+ concentration. They exhibit a 50-fold increase in fluorescence upon calcium binding and offer a range of wavelengths that can be used in conjunction with GFP or green-fluorescent dyes for multiplexing. Rhod-2, AM (Cat. No. R1245MP), in particular, localizes to mitochondria and can be used with flow cytometry.
-Membrane potential: A distinctive feature of the early stages of apoptosis is the disruption of the mitochondria, including changes in membrane and redox potential. We offer a range of products specifically designed to assay mitochondrial membrane potential in live cells by flow cytometry, with minimal disruption of cellular function. The MitoProbe family of mitochondrial stains (Cat. Nos. M34150, M34151, and M34152) provide quick, easy, and reliable flow cytometric detection of the loss of mitochondrial membrane potential that occurs during apoptosis. MitoTracker dyes (Cat. Nos. M7510 and M7512) are membrane potential-dependent probes for staining mitochondria in live cells. The staining pattern of MitoTracker dyes is retained throughout subsequent flow cytometry immunocytochemistry, DNA end labeling, in situ hybridization, or counterstaining steps. The Mitochondrial Permeability Transition Pore Assay (Cat. No. M34153) provides a more direct method of measuring mitochondrial permeability transition pore opening than assays relying on mitochondrial membrane potential alone. The mitochondrial permeability transition pore (MPTP) is a non-specific channel formed by components from the inner and outer mitochondrial membranes, and appears to be involved in the release of mitochondrial components during cell death.
-Phagocytosis: In phagocytosis, cells internalize particulate matter such as microorganisms, and this process is important for immune responses and during the clearance of apoptotic cells. Probes for studying phagocytosis include BioParticles indicators—bacteria and yeast labeled with fluorescent dyes.
-Tracking phagocytosis using a quench/wash-based assay can report on simple uptake, or a pH indicator can be used to monitor stages in the pathway. We have no-wash assays labeled with pHrodo Red or Green (Cat. Nos. A10010, P35361, P35364, P35365, P35366, and P35367) and no-wash assays for whole blood (Cat. Nos. A10025, A10026, P35381, and P35382), all suitable for flow cytometry.
-pH changes: Sensitive pH determinations can be made in a physiological range using either fluorescent intensity or ratiometric measurements. pHrodo dyes (Cat. Nos. P35373 and P35372) provide signal intensity modulation from pH 2 to pH 9 and with a choice of fluorescent wavelengths. Tracking internalization of fluorescent dextran is a routine method for analyzing pH changes in cellular compartments. Dextran conjugates of pHrodo dyes (Cat. Nos. P35368 and P10361) provide the most complete solution by allowing discrimination of vesicles from early endosomes to lysosomes, with no quench or wash required.
-Reactive oxygen species: Cells that are environmentally stressed usually contain greatly increased levels of reactive oxygen species (ROS). CellROX reagents are fluorogenic probes developed for the detection and quantitation of ROS in live cells. These cell-permeant reagents are non-fluorescent or very weakly fluorescent in the reduced state; however, when oxidized, they become brightly fluorescent and remain localized within the cell. We offer CellROX Green (Cat. No. C10492), CellROX Orange (Cat. No. C10493), and CellROX Deep Red (Cat. No. C10491) Assay Kits validated for flow cytometry.

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

Citations & References (129)

Citations & References
Abstract
Normal fertilization occurs with eggs lacking the integrin alpha6beta1 and is CD9-dependent.
Authors:Miller BJ, Georges-Labouesse E, Primakoff P, Myles DG
Journal:J Cell Biol
PubMed ID:10851025
'Previous results, based on inhibition of fertilization by an anti-alpha6 integrin mAb (GoH3), suggest that the alpha6beta1 integrin on mouse eggs functions as the receptor for sperm (Almeida, E.A., A.P. Huovila, A.E. Sutherland, L.E. Stephens, P.G. Calarco, L. M. Shaw, A.M. Mercurio, A. Sonnenberg, P. Primakoff, D.G. Myles, and J.M. ... More
Acetylcholine-induced calcium signaling and contraction of airway smooth muscle cells in lung slices.
Authors:Bergner A, Sanderson MJ
Journal:J Gen Physiol
PubMed ID:11815668
'The Ca(2+) signaling and contractility of airway smooth muscle cells (SMCs) were investigated with confocal microscopy in murine lung slices (approximately 75-microm thick) that maintained the in situ organization of the airways and the contractility of the SMCs for at least 5 d. 10--500 nM acetylcholine (ACH) induced a contraction ... More
Intracellular astrocyte calcium waves in situ increase the frequency of spontaneous AMPA receptor currents in CA1 pyramidal neurons.
Authors:Fiacco TA, McCarthy KD
Journal:J Neurosci
PubMed ID:14736858
'Spontaneous neurotransmitter release and activation of group I metabotropic glutamate receptors (mGluRs) each play a role in the plasticity of neuronal synapses. Astrocytes may contribute to short- and long-term synaptic changes by signaling to neurons via these processes. Spontaneous whole-cell AMPA receptor (AMPAR) currents were recorded in CA1 pyramidal cells ... More
The sources and sequestration of Ca(2+) contributing to neuroeffector Ca(2+) transients in the mouse vas deferens.
Authors:Brain KL, Cuprian AM, Williams DJ, Cunnane TC
Journal:J Physiol
PubMed ID:14500773
'The detection of focal Ca(2+) transients (called neuroeffector Ca(2+) transients, or NCTs) in smooth muscle of the mouse isolated vas deferens has been used to detect the packeted release of ATP from nerve terminal varicosities acting at postjunctional P2X receptors. The present study investigates the sources and sequestration of Ca(2+) ... More
Control of IP(3)-mediated Ca2+ puffs in Xenopus laevis oocytes by the Ca2+-binding protein parvalbumin.
Authors:John LM, Mosquera-Caro M, Camacho P, Lechleiter JD
Journal:J Physiol
PubMed ID:11507154
'1. Elementary events of Ca2+ release (Ca2+ puffs) can be elicited from discrete clusters of inositol 1,4,5 trisphosphate receptors (IP(3)Rs) at low concentrations of IP(3). Ca(2+) puffs have rarely been observed unless elicited by either hormone treatment or introduction of IP(3) into the cell. However, cells appear to have sufficient ... More