FluoSpheres™ Carboxylate-Modified Microspheres
FluoSpheres™ Carboxylate-Modified Microspheres
Invitrogen™

FluoSpheres™ Carboxylate-Modified Microspheres

Consiga la fluorescencia más brillante gracias a las microesferas FluoSphere modificadas con carboxilos, disponibles en diferentes colores y tamaños de partículas.
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Número de catálogoDiámetro (métrico)ColorExcitación/emisiónCantidad
F8795
también denominado F-8795
0,04 μmAmarillo-Verde505/515 nm1 mL
F88030,1 μmAmarillo-verde505/515 nm10 mL
F88161,0 μmCarmesí625/645 nm2 mL
F88231,0 μmAmarillo-verde505/515 nm10 mL
F88010,1 μmRojo580/605 nm10 mL
F88110,2 μmAmarillo-verde505/515 nm10 mL
F88070,2 μmRojo oscuro660/680 nm2 mL
F107200,04 μmAmarillo-verde, Naranja, Rojo, Rojo oscuro505/515, 540/560, 580/605, 660/680 nm1 ml (cada uno)
F208810,2 μmNaranja365/610 nm2 mL
F8783
también denominado F-8783
0,02 μmRojo oscuro660/680 nm2 mL
F87860,02 μmRojo580/605 nm10 mL
F88130,5 μmAmarillo-verde505/515 nm10 mL
F88201,0 μmNaranja540/560 nm10 mL
F88252,0 μmRojo Nilo535/575 nm2 mL
F88272,0 μmAmarillo-verde505/515 nm2 mL
F8781
también denominado F-8781
0,02 μmAzul365/415 nm10 mL
F8782
también denominado F-8782
0,02 μmCarmesí625/645 nm2 mL
F87840,02 μmRojo Nilo535/575 nm10 mL
F87870,02 μmAmarillo-verde505/515 nm10 mL
F8789
también denominado F-8789
0,04 μmRojo oscuro660/680 nm1 mL
F8792
también denominado F-8792
0,04 μmNaranja540/560 nm1 mL
F87930,04 μmRojo580/605 nm1 mL
F87940,04 μmRojo-naranja565/580 nm1 mL
F87970,1 μmAzul350/440 nm10 mL
F87990,1 μmInfrarrojo715/755 nm1 mL
F8800
también denominado F-8800
0,1 μmNaranja540/560 nm10 mL
F88050,2 μmAzul365/415 nm10 mL
F88060,2 μmCarmesí625/645 nm2 mL
F88090,2 μmNaranja540/560 nm10 mL
F88100,2 μmRojo580/605 nm10 mL
F88120,5 μmRojo580/605 nm10 mL
F88141,0 μmAzul365/415 nm10 mL
F88151,0 μmAzul350/440 nm10 mL
F88191,0 μmRojo Nilo535/575 nm10 mL
F88211,0 μmRojo580/605 nm10 mL
F8824
también denominado F-8824
2,0 μmAzul365/415 nm2 mL
F88262,0 μmRojo580/605 nm2 mL
Número de catálogo F8795
también denominado F-8795
Precio (CLP)
-
Diámetro (métrico):
0,04 μm
Color:
Amarillo-Verde
Excitación/emisión:
505/515 nm
Cantidad:
1 mL

Utilice nuestra amplia selección de microesferas modificadas con carboxilatos FluoSpheres para realizar fácilmente citometría de flujo, microscopía, HTS, HCS, inmunoensayo, así como otras aplicaciones de laboratorio. Los gránulos FluoSphere se pueden utilizar en adsorción pasiva o activa, acoplamiento covalente de proteínas, ácidos nucleicos y biomoléculas para aplicaciones de captura de partículas. Las microesferas FluoSphere están cargadas de colorantes fluorescentes exclusivos, lo que las convierte en las microesferas más brillantes disponibles.

Visualice la fluorescencia más brillante para aplicaciones de laboratorio, como microscopía de fluorescencia, citometría de flujo, HTS, HCS y rastreo celular, gracias a nuestras microesferas FluoSphere modificadas con carboxilatos, fabricadas con microesferas de poliestireno y cargadas con diferentes colorantes patentados. Gracias al uso de métodos de coloración especializados, permite que todas las moléculas de colorante fluorescente estén contenidas dentro de cada microesfera de poliestireno, en lugar de en la superficie. Este entorno de protección dentro del gránulo protege el tinte de efectos medioambientales perjudiciales, como la decoloración fotográfica. Nuestras microesferas modificadas con carboxilato están recubiertas con un polímero hidrofílico que contiene múltiples ácidos carboxílicos para la fijación covalente de los ligandos. Existen diversos tamaños de partículas disponibles para diferentes usos y experimentos de investigación.
For Research Use Only. Not for use in diagnostic procedures.
Especificaciones
Excitación/emisión505/515 nm
Línea de productosFLUOSPHERES
Cantidad1 mL
Modificación de la superficieCarboxilato
ColorAmarillo-Verde
Diámetro (métrico)0,04 μm
Para utilizar con (aplicación)Microscopía de fluorescencia
MaterialPoliestireno
Tipo de productoMicroesfera modificada con carboxilatos
Unit SizeEach
Contenido y almacenamiento
Almacenar en el refrigerador (2 °C a 8 °C) y proteger de la luz.

Preguntas frecuentes

I read that carboxylate-modified latex (CML) beads have a "fluffy coat" of carboxyl groups on their surface. What is meant by this?

The CML beads have a high density of carboxyl groups at the surface. The surface layer is quite hydrophilic and at the appropriate pH (pH>5), are charged; due to electrostatic repulsion, this type of surface is 3-dimensional and may be considered analogous to the fuzz on a tennis ball.

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

I have some FluoSpheres polystyrene microspheres, with 20 nm diameter. They are aggregating a lot. What can I do about it?

The smaller the microspheres, the greater the propensity to aggregate. But the aggregation is not irreversible. Sonicate in a bath sonicator or vortex to disperse, just prior to use. You can also add a small concentration of Tween-20 or Triton X-100 (unless you are using them in a live-cell system).

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

I sonicated my 2.0 µm carboxylate-modified microspheres, as recommended, but saw foaming (bubbles) on top of the solution. Should I be concerned?

Use of a bath sonicator is recommended to help break up any aggregated microspheres. The foaming is from Tween-20, which is in the stock solution to help prevent aggregation. It is normal and expected to see bubbles from this. Do not use a probe sonicator, which would cause damage to the microspheres (as well as much more bubbling).

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

What is the warranty for FluoSpheres microspheres?

The warranty period for FluoSpheres microspheres is 1-year from the date of shipment.

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

After washing and centrifugation, there was only a very small pellet left of my microsphere beads and the solution was transparent. Why is this?

Centrifugation is not an effective way to collect smaller microspheres; many particles remain in the solution even if you can visualize a small pellet. For beads less than 1 µm in diameter, we recommend washing by either:

Cross-flow filtration, as these particles have a very high compression modulus and can withstand high g-forces without risk of harm or dialysis with a 500 kDa MWCO
Note: Microspheres greater than 1 µm in diameter can be centrifuged at 1,300 rpm.

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

Citations & References (8)

Citations & References
Abstract
Nano-sized fluorescent particles as new tracers for sentinel node detection: experimental model for decision of appropriate size and wavelength.
Authors:Nakajima M, Takeda M, Kobayashi M, Suzuki S, Ohuchi N
Journal:Cancer Sci
PubMed ID:15958058
'The concepts of made-to-order and low-invasiveness medicines are becoming widely accepted. A treatment for cancer, with minimum invasive surgery and without lymph nodes dissection based on sentinel lymph node (SN) navigation surgery, would adhere to these concepts. Dyes and/or radioisotopes are employed for SN detection in standard methods, however, each ... More
Why molecules move along a temperature gradient.
Authors:Duhr S, Braun D
Journal:Proc Natl Acad Sci U S A
PubMed ID:17164337
'Molecules drift along temperature gradients, an effect called thermophoresis, the Soret effect, or thermodiffusion. In liquids, its theoretical foundation is the subject of a long-standing debate. By using an all-optical microfluidic fluorescence method, we present experimental results for DNA and polystyrene beads over a large range of particle sizes, salt ... More
Oxidized low-density lipoprotein promotes mature dendritic cell transition from differentiating monocyte.
Authors:Perrin-Cocon L, Coutant F, Agaugué S, Deforges S, André P, Lotteau V
Journal:J Immunol
PubMed ID:11564795
'Proinflammatory oxidized phospholipids are generated during oxidative modification of low-density lipoproteins (LDL). The production of these proinflammatory oxidized phospholipids is controlled by secreted enzymes that circulate as proteins complexed with LDL and high-density lipoprotein. During the acute phase response to tissue injury, profound changes occur in lipoprotein enzymatic composition that ... More
I5S: wide-field light microscopy with 100-nm-scale resolution in three dimensions.
Authors:Shao L, Isaac B, Uzawa S, Agard DA, Sedat JW, Gustafsson MG,
Journal:Biophys J
PubMed ID:18326649
A new type of wide-field fluorescence microscopy is described, which produces 100-nm-scale spatial resolution in all three dimensions, by using structured illumination in a microscope that has two opposing objective lenses. Illumination light is split by a grating and a beam splitter into six mutually coherent beams, three of which ... More
Determination of absolute protein numbers in single synapses by a GFP-based calibration technique.
Authors:Sugiyama Y, Kawabata I, Sobue K, Okabe S,
Journal:Nat Methods
PubMed ID:16118638
To build a quantitative model of molecular organization of neurons, it is essential to have information about the number of protein molecules at individual synapses. Here we developed a method to estimate absolute numbers of individual proteins at actual excitatory synapses by calibrating the fluorescence intensity of microspheres with single ... More