Escherichia coli (K-12 strain) BioParticles™, Alexa Fluor™ 488 conjugate
<i>Escherichia coli</i> (K-12 strain) BioParticles&trade;, Alexa Fluor&trade; 488 conjugate
Invitrogen™

Escherichia coli (K-12 strain) BioParticles™, Alexa Fluor™ 488 conjugate

La línea de productos Molecular Probes™ BioParticles™ está formada por una serie de bacterias y levaduras marcadas con fluorescencia yMás información
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Número de catálogoCantidad
E132312 mg
Número de catálogo E13231
Precio (MXN)
-
Cantidad:
2 mg
La línea de productos Molecular Probes™ BioParticles™ está formada por una serie de bacterias y levaduras marcadas con fluorescencia y matadas por calor o químicamente en una variedad de tamaños, formas y antigenicidades naturales. Estos productos fluorescentes de BioParticles™ se han empleado para estudiar la fagocitosis por microscopia de fluorescencia, la espectrofluorometría cuantitativa y la citometría de flujo.

Ofrecemos los conjugados BioParticles™ E. coli (cepa K-12), S. aureus (cepa Wood, sin proteína A) y zymosan (S. cerevisiae) con marcado covalente y distintos fluoróforos diferentes (se ha tenido especial cuidado para eliminar el colorante libre después de la conjugación). A diferencia de la fluorescencia de los conjugados BioParticles™ marcados con fluoresceína, que se encuentra parcialmente suprimida en ambientes ácidos, la fluorescencia de los conjugados de colorante Alexa Fluor™, BODIPY™ FL, tetrametilrodamina y Texas Red™ es uniformemente intensa en el rango de pH de 3 a 10.

Especificaciones de BioParticles:
• Etiqueta (Ex/Em): Alexa Fluor™ 488 (∼ 495/519 nm)
• Partícula: E. coli (cepa K-12)
Reactivo de opsonización disponible


Uso de productos BioParticles
Los conjugados BioParticles™ se suministran en forma de polvos liofilizados. Hay aproximadamente 3 x 108 partículas de E. coli o S. aureus por mg sólido y aproximadamente 2 x 107 partículas de zimosano por mg sólido. Los conjugados BioParticles™ pueden reconstituirse en el tampón que prefiera para su uso en ensayos de fagocitosis. La fluorescencia de los conjugados BioParticles™ que están unidos a la superficie celular (pero no internalizados) puede suprimirse mediante bromuro de etidio, azul de tripano u otros supresores. Además de las aplicaciones celulares, los conjugados fluorescentes BioParticles™ pueden ser eficaces como referencias de calibración de citómetros de flujo al clasificar bacterias y mutantes de la levadura. Estas pequeñas partículas también pueden ser referencias útiles para estudios sobre la dispersión de la luz porque sus tamaños y formas difieren de manera característica.

Encuentre más productos BioParticles™
Ofrecemos una amplia gama de productos BioParticles™ E. coli (K-12 strain), S. aureus (cepa Wood, sin proteína A) y zymosan (S. Cerevisiae)) marcados con colorante y sin marcar. Para obtener más información sobre estos productos y sus aplicaciones, consulte Probes for Following Receptor Binding and Phagocytosis—Section 16.1 (Sondas para seguir la unión de receptores y la fagocitosis, sección 16.1) en el manual de Molecular Probes™.

Para ensayos de endocitosis sensibles al pH, consulte nuestros conjugados pHrodo™ BioParticles™.

Para uso exclusivo en investigación. No apto para uso diagnóstico o terapéutico en humanos ni en animales.
Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.
Especificaciones
Tipo de célulaCélula de mamífero
Método de detecciónFluorescente
Tipo de coloranteAlexa Fluor™ 488
FormularioSólido
Cantidad2 mg
Condiciones de envíoHielo seco
EspecieE. coli
Para utilizar con (equipo)Microscopio de fluorescencia
Línea de productosAlexa Fluor, BioParticles
Tipo de productoConjugado E. coli
Unit SizeEach
Contenido y almacenamiento
Almacenar en el congelador (de – 5 a – 30 °C) y proteger de la luz.

Preguntas frecuentes

How are the Escherichia coli (K-12 strain) BioParticles, Alexa Fluor 488 conjugate supplied?

The Escherichia coli (K-12 strain) BioParticles, Alexa Fluor 488 conjugate are supplied as lyophilized powder in a 2 mg unit size. There are approximately 3 x 10E8 E. coli particles per mg solid.

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

What is the particle size of Escherichia coli (K-12 strain) BioParticles, Alexa Fluor™ 488 conjugate (Cat. No. E13231)?

The particle size of Escherichia coli (K-12 strain) BioParticles fluorescent conjugates are approximately 0.2 micron wide and 2-3 micron long.

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

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.

Citations & References (6)

Citations & References
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
PLD$ is involved in phagocytosis of microglia: expression and localization changes of PLD4 are correlated with activation state of microglia.
Authors:Otani Y, Yamaguchi Y, Sato Y, Furuichi T, Ikenaka K, Kitani H, Baba H,
Journal:PLoS One
PubMed ID:22102906
Phospholipase D4 (PLD4) is a recently identified protein that is mainly expressed in the ionized calcium binding adapter molecule 1 (Iba1)-positive microglia in the early postnatal mouse cerebellar white matter. Unlike PLD1 and PLD2, PLD4 exhibits no enzymatic activity for conversion of phosphatidylcholine into choline and phosphatidic acid, and its ... More
Live cell imaging of zebrafish leukocytes.
Authors:Hall C, Flores MV, Crosier K, Crosier P,
Journal:Methods Mol Biol
PubMed ID:19378109
Zebrafish are ideally suited for the live imaging of early immune cell compartments. Macrophages that initially appear on the yolk surface prior to the onset of circulation are the first functional immune cells within the embryo, predating the emergence of the first granulocytic cells-the heterophilic neutrophils. Both cell types have ... More