Oregon Green™ 488 BAPTA-1, AM, membrangängig - Spezialverpackung
Invitrogen™

Oregon Green™ 488 BAPTA-1, AM, membrangängig - Spezialverpackung

Markierte Calcium-Indikatoren sind Moleküle, die nach Ca2+-Bindung eine erhöhte Fluoreszenz zeigen. Sie werden bei vielen Untersuchungen zur Signalübertragung bei CalciumWeitere Informationen
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KatalognummerMenge
O680710 x 50 μg
Katalognummer O6807
Preis (EUR)
626,65
Exklusiv online
660,00
Ersparnis 33,35 (5%)
Each
Menge:
10 x 50 μg
Preis (EUR)
626,65
Exklusiv online
660,00
Ersparnis 33,35 (5%)
Each
Markierte Calcium-Indikatoren sind Moleküle, die nach Ca2+-Bindung eine erhöhte Fluoreszenz zeigen. Sie werden bei vielen Untersuchungen zur Signalübertragung bei Calcium verwendet, z. B. Messung intrazellulärer Ca2+ nach Ca2+-Zufluss und -Freisetzung sowie Bildgebung der Multiphotonenanregung von Ca2+ in lebendem Gewebe. Zellen können mit den AM-Esterformen dieser Calcium-Indikatoren beladen werden, indem der gelöste Indikator direkt den Schalen mit den kultivierten Zellen hinzugefügt wird. Das Fluoreszenzsignal aus diesen Zellen wird in der Regel mittels Fluoreszenzmikroskopie, Fluoreszenz-Mikrotiterplattenassays oder Durchflusszytometrie gemessen.

Weitere Informationen zu Ionenindikatoren wie Calcium-, Kalium-, pH-Wert- und Membranpotentialindikatoren ›

Calciumindikator(AM Ester)-Spezifikationen:
• Markierung (Ex/Em): Oregon Green™ 488 BAPTA-1 (494/523 nm)
• Steigerung der Fluoreszenzintensität bei Bindung an Ca2+: ∼14-fach
• Zeigt Fluoreszenzerhöhung nach Ca2+ Bindung mit geringer Wellenlängenverschiebung


Spektraleigenschaften von Molecular Probes™ Calciumindikatoren
Diese Sonden werden durch sichtbares Licht angeregt, und da die für die Anregung erforderliche Energie gering ist, wird das Potenzial für zelluläre Photoschäden reduziert. Häufig verwendete Laser-basierte Geräte (d. h. konfokale Laser-Scanning-Mikroskope) sind in der Lage, diese Indikatoren effizient zu erregen. Ihre Emissionen liegen in den Regionen des Spektrums, in denen zelluläre Autofluoreszenz- und Streuungshintergründe oft weniger ein Problem darstellen.

Größere Auswahl fluoreszierender Calciumindikatoren
Wir bieten eine große Auswahl von Molecular Probes™ Calciumindikatoren für den Einsatz in verschiedenen experimentellen Szenarien, zum Beispiel Dextran-Versionen für reduzierte Leckage und Kompartimentierung sowie BAPTA-Konjugate zur Erkennung von Calcium-Transienten mit hoher Amplitude. Weitere Informationen finden Sie unter Fluorescent Ca2+ Indicators Excited with Visible Light, Abschnitt 19.3 im Molecular Probes™ Handbuch.

Für UV-anregbare Ca2+-Indikatoren, Protein-basierte Ca2+-Indikatoren, Konjugate von Ca2+-Indikatoren und fluoreszenzbasierte Indikatoren anderer Metallionen (d. h. Mg2+, Zn2+) siehe Indikatoren für Ca2+, Mg2+, Zn2+ und andere Metallionen, Kapitel 19 im Molecular Probes™ Handbuch.

Nur für Forschungszwecke. Nicht für therapeutische oder diagnostische Zwecke an Tieren und Menschen bestimmt.
Nur für Forschungszwecke. Nicht zur Verwendung bei diagnostischen Verfahren.
Specifications
NachweisverfahrenFluoreszent
FarbstofftypFarbstoffbasiertes Fluoreszenzmittel
Menge10 x 50 μg
VersandbedingungRaumtemperatur
Zur Verwendung mit (Anwendung)Viabilität und Proliferation von Zellen
Zur Verwendung mit (Geräte)Fluoreszenzmikroskop, Durchflusszytometer, Mikrotiterplatten-Lesegerät
ProduktlinieOregon Green
ProdukttypFärben
Unit SizeEach
Inhalt und Lagerung
Im Tiefkühlgerät lagern (-5 bis -30 °C).

Häufig gestellte Fragen (FAQ)

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.

Zitierungen und Referenzen (129)

Zitierungen und Referenzen
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