Staphylococcus aureus (Wood strain without protein A) BioParticles™, Alexa Fluor™ 488 conjugate
<i>Staphylococcus aureus</i> (Wood strain without protein A) BioParticles&trade;, Alexa Fluor&trade; 488 conjugate
Invitrogen™

Staphylococcus aureus (Wood strain without protein A) BioParticles™, Alexa Fluor™ 488 conjugate

Die Molecular Probes™ BioParticles™ Produktlinie besteht aus einer Reihe von Fluoreszenz-markierten, durch Hitze oder chemisch abgetöteten Bakterien und Hefen inWeitere Informationen
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KatalognummerMenge
S233712 mg
Katalognummer S23371
Preis (EUR)
315,24
Special offer
Online exclusive
Endet: 15-Mar-2026
426,00
Ersparnis 110,76 (26%)
Each
Zum Warenkorb hinzufügen
Menge:
2 mg
Preis (EUR)
315,24
Special offer
Online exclusive
Endet: 15-Mar-2026
426,00
Ersparnis 110,76 (26%)
Each
Zum Warenkorb hinzufügen
Die Molecular Probes™ BioParticles™ Produktlinie besteht aus einer Reihe von Fluoreszenz-markierten, durch Hitze oder chemisch abgetöteten Bakterien und Hefen in verschiedenen Größen, Formen und natürlichen Antigenitäten. Diese fluoreszierenden BioParticles™ Produkte wurden zur Untersuchung der Phagozytose mittels Fluoreszenzmikroskopie, quantitativer Spektralfluorometrie und Durchflusszytometrie eingesetzt.

Wir bieten E. coli (K-12-Stamm), S. aureus (Wood-Stamm, ohne Protein A) und Zymosan (S. cerevisiae) BioParticles™ Konjugate, die kovalent mit einer Vielzahl von verschiedenen Fluorophoren markiert sind (dabei wurde besondere Sorgfalt darauf verwendet, freien Farbstoff nach der Konjugation zu entfernen). Im Gegensatz zur Fluoreszenz von Fluorescein-markierten BioParticles™ Konjugaten, die in sauren Umgebungen teilweise gequencht wird, ist die Fluoreszenz von Alexa Fluor™, BODIPY™ FL, Tetramethylrhodamin und Texas Red™ Farbstoffkonjugaten über den pH-Bereich 3 bis 10 gleichmäßig intensiv.

BioParticles Spezifikationen:
• Markierung (Ex/Em): Alexa Fluor™ 488 (∼ 495/519 nm)
• Partikel: S. aureus (Wood-Stamm, ohne Protein A)
Opsonierendes Reagenz erhältlich


Verwendung von BioParticles Produkten
BioParticles™ Konjugate werden als gefriergetrocknete Pulver geliefert. Enthält ca. 3 x 108 E. coli- oder S. aureus-Partikel pro mg Feststoff und ca. 2 x 107 Zymosan-Partikel pro mg Feststoff. BioParticles™ Konjugate können zur Verwendung in Phagozytose-Assays im Puffer Ihrer Wahl rekonstituiert werden. Die Fluoreszenz von BioParticles™ Konjugaten, die an die Zelloberfläche gebunden (aber nicht internalisiert) sind, kann durch Ethidiumbromid, Trypanblau oder andere Quencher gelöscht werden. Zusätzlich zu zellulären Anwendungen können fluoreszierende BioParticles™ Konjugate in der Durchflusszytometrie als Kalibrierungsreferenzen beim Sortieren von Bakterien und Hefemutanten wirken Diese kleinen Partikel können auch nützliche Referenzen für Studien zur Lichtstreuung sein, da sich ihre Größen und Formen in charakteristischer Weise unterscheiden.

Weitere BioParticles™ Produkte
Wir bieten eine große Auswahl an farbstoffmarkierten und nicht markierten E. coli (K-12-Stamm), S. aureus (Wood-Stamm, ohne Protein A) und Zymosan (S. cerevisiae) BioParticles™ Produkten an. Weitere Informationen über diese Produkte und ihre Anwendungen finden Sie im Molecular Probes™ Handbuch unter Sonden für die Verfolgung von Rezeptorbindung und Phagozytose – Abschnitt 16.1.

Informationen zu pH-empfindlichen Endozytose-Assays finden Sie bei unseren pHrodo™ BioParticles™ Konjugaten.

Nur für Forschungszwecke. Nicht für therapeutische oder diagnostische Zwecke bei Menschen oder Tieren vorgesehen.
Nur für Forschungszwecke. Nicht zur Verwendung bei diagnostischen Verfahren.
Specifications
NachweisverfahrenFluoreszent
FarbstofftypAlexa Fluor™ 488
FormLyophilisiertes Pulver
Menge2 mg
VersandbedingungRaumtemperatur
SpeziesS. aureus
Zur Verwendung mit (Geräte)Fluoreszenzmikroskop
ProduktlinieAlexa Fluor, BioParticles
ProdukttypBiopartikel, Konjugat
pH3 bis 10
Unit SizeEach
Inhalt und Lagerung
Bei -5 bis -30 °C lagern und vor Licht schützen.

Häufig gestellte Fragen (FAQ)

Are the Invitrogen BioParticles products sterile?

While the bacteria have been attenuated with formaldehyde and alcohol desiccation, the BioParticles products are not considered sterile, and we do not recommend incubation of more than 4 hours. This applies to all of our dye-labeled (pHrodo, Alexa Fluor, etc.) and unlabeled BioParticles products.

What is the type of bond that attaches the dyes to the BioParticles probes?

We use amine-reactive dyes to covalently attach fluorescent dyes to all of our BioParticles probes such as the Escherichia coli (K-12 strain) BioParticles probes, Staphylococcus aureus (Wood strain without protein A) BioParticles, and the Zymosan A (S. cerevisiae) BioParticles probes.

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

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.

What can the BioParticles product line be used for?

Fluorescent Bioparticles have been employed to study phagocytosis by fluorescence microscopy, quantitative spectrofluorometry, and flow cytometry. We offer E.Coli, S. aureus, and zymosan BioParticles conjugates covalently labeled with a variety of different fluorophores.

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

Zitierungen und Referenzen (6)

Zitierungen und Referenzen
Abstract
Extracellular Matrix Lumican Promotes Bacterial Phagocytosis, and Lum-/- Mice Show Increased Pseudomonas aeruginosa Lung Infection Severity.
Authors:Shao H, Lee S, Gae-Scott S, Nakata C, Chen S, Hamad AR, Chakravarti S,
Journal:J Biol Chem
PubMed ID:22865855
'Phagocytosis is central to bacterial clearance, but the exact mechanism is incompletely understood. Here, we show a novel and critical role for lumican, the connective tissue extracellular matrix small leucine-rich repeat proteoglycan, in CD14-mediated bacterial phagocytosis. In Psuedomonas aeruginosa lung infections, lumican-deficient (Lum(-/-)) mice failed to clear the bacterium from ... More
Multipotent stem cells from trabecular meshwork become phagocytic TM cells.
Authors:Du Y, Roh DS, Mann MM, Funderburgh ML, Funderburgh JL, Schuman JS,
Journal:Invest Ophthalmol Vis Sci
PubMed ID:22297497
'To isolate and characterize stem cells from human trabecular meshwork (TM) and to investigate the potential of these stem cells to differentiate into TM cells. Human trabecular meshwork stem cells (TMSCs) were isolated as side population cells by fluorescence-activated cell sorting or isolated by clonal cultures. Passaged TMSCs were compared ... More
Antibody to Langerin/CD207 localizes large numbers of CD8alpha+ dendritic cells to the marginal zone of mouse spleen.
Authors:Idoyaga J, Suda N, Suda K, Park CG, Steinman RM,
Journal:Proc Natl Acad Sci U S A
PubMed ID:19168629
Dendritic cells (DCs) are strategically positioned to take up antigens and initiate adaptive immunity. One DC subset expresses CD8alphaalpha in mice and is specialized to capture dying cells and process antigens for MHC class I  ... More
Functional dissociation of the basolateral transcytotic compartment from the apical phago-lysosomal compartment in human osteoclasts.
Authors:Meagher J, Zellweger R, Filgueira L,
Journal:J Histochem Cytochem
PubMed ID:15872059
Tartrate-resistant acid phosphatase (TRAP) is essential for elimination of Staphylococcus aureus, the main infectious agent responsible for osteomyelitis. This in vitro study investigated uptake and processing of fluorescence-labeled S. aureus by human osteoclasts and dendritic cells. The cells were stained for TRAP and the acidic compartment using a fluorescence-based protocol. ... More
Heterogeneity in macrophage phagocytosis of Staphylococcus aureus strains: high-throughput scanning cytometry-based analysis.
Authors:DeLoid GM, Sulahian TH, Imrich A, Kobzik L,
Journal:PLoS One
PubMed ID:19593389
Alveolar macrophages (AMs) can phagocytose unopsonized pathogens such as S. aureus via innate immune receptors, such as scavenger receptors (SRs). Cytoskeletal events and signaling pathways involved in phagocytosis of unopsonized bacteria likely govern the fate of ingested pathogens, but are poorly characterized. We have developed a high-throughput scanning cytometry-based assay ... More