FluoSpheres™ Polystyrene Microspheres, 1.0 μm, blue-green fluorescent (430/465), for tracer studies
FluoSpheres™ Polystyrene Microspheres, 1.0 μm, blue-green fluorescent (430/465), for tracer studies
Invitrogen™

FluoSpheres™ Polystyrene Microspheres, 1.0 μm, blue-green fluorescent (430/465), for tracer studies

Microspheres (also called latex beads or latex particles) are spherical particles in the colloidal size range that are formed from자세히 알아보기
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카탈로그 번호수량
F130805 mL
카탈로그 번호 F13080
제품 가격(KRW)
545,000
온라인 행사
Ends: 31-Dec-2025
681,000
할인액 136,000 (20%)
Each
카트에 추가하기
수량:
5 mL
제품 가격(KRW)
545,000
온라인 행사
Ends: 31-Dec-2025
681,000
할인액 136,000 (20%)
Each
카트에 추가하기
Microspheres (also called latex beads or latex particles) are spherical particles in the colloidal size range that are formed from an amorphous polymer such as polystyrene. Our Molecular Probes™ FluoSpheres™ beads are manufactured using high-quality, ultraclean polystyrene and are loaded with a variety of our proprietary dyes to create intensely fluorescent beads that typically show little or no photobleaching, even when excited with the intense illumination required for fluorescence microscopy.

For tracking particles and cells, tracing fluid dynamics, discriminating the size dependence of uptake or transport in vivo, etc., we offer more concentrated, 0.04 μm diameter FluoSpheres™ microspheres preparations (5% solids) that lack the sodium azide preservative present in the majority of our FluoSpheres™ products. The 0.04 μm particles are small enough to be microinjected or to be taken up by phagocytosis.

We also offer 1.0 μm FluoSpheres™ microsphere preparations that contain a much higher dye content than our other FluoSpheres™ products. This allows stronger signals to be generated using fewer microspheres per tracing experiment.

In many biological systems, the concentrated fluorescence and spherical shape of the FluoSpheres™ beads permit them to be detected against a relatively high but diffuse background fluorescence. Typically for these types of studies, the microspheres and the fluorescent dyes they contain are first extracted from the tissue sample, and then the fluorescence is quantified on a spectrofluorometer or fluorescence microplate reader. The use of fluorescent microspheres eliminates the radiation hazards and disposal hurdles associated with radiolabeled microspheres.

FluoSpheres™ Microsphere Specifications:

Label (Ex/Em): Blue-green fluorescent (430/465)
Nominal bead diameter: 1.0 μm
Coupling surface: Carboxylate
Solids: 2%

Characteristics of the Carboxylate Coupling Surface
Carboxylate-modified FluoSpheres™ beads have a high density of pendent carboxylic acids on their surface, making them suitable for covalent coupling of proteins and other amine-containing biomolecules using water-soluble carbodiimide reagents such as EDAC.

Choices for FluoSpheres™ Fluorescent Microspheres
In addition to microspheres for tracing, investigate our complete offering of fluorescent microspheres products. Among those products you’ll find beads with these variations:
• Ten fluorescent colors
• Ten nominal bead diameters: 0.02 μm, 0.04 μm, 0.1 μm, 0.2 μm, 0.5 μm, 1.0 μm, 2.0 μm, 4.0 μm, 10.0 μm, and 15.0 μm
• Four surface modifications for protein coupling: carboxylate, sulfate, aldehyde-sulfate, amine
• Microspheres that are additionally precoupled with streptavidin, NeutrAvidin, biotin, europium, and platinum

Choices for Unstained Microspheres
We also offer hundreds of choices for UltraClean™ surfactant-free microspheres for research and commercial applications.

We’ll Make a Custom Microsphere Product for You
We will prepare custom orders upon request. For example, FluoSpheres™ beads can be prepared with intensities that are lower than those of our regular selection, a desirable feature in some multicolor applications. Our custom conjugation service is efficient and confidential, and we stand by quality of our work. We are ISO 13485:2000 certified.

For Research Use Only. Not intended for animal or human therapeutic or diagnostic use.
For Research Use Only. Not for use in diagnostic procedures.
사양
농도1 x 1010 beads/mL
제품라인FLUOSPHERES
수량5 mL
배송 조건Room Temperature
표면 수정Other Modification or Label
색상Blue-Green
직경(미터법)1 μm
물질Polystyrene
제품 유형Microsphere
Unit SizeEach
구성 및 보관
Store in refrigerator (2–8°C) and protect from light.

자주 묻는 질문(FAQ)

I want to use fluorescent microspheres for blood tracing studies. What functional group should be on the surface?

We offer FluoSpheres fluorescent microspheres for tracer studies that are 1, 10 and 15 µm in diameter, with various wavelengths. If those sizes or available colors are not optimal for your application, then we recommend carboxylate-modified microspheres, which are available in a wide range of sizes and colors.

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.

I've had my microspheres for over a year, and I'm wondering if they're still good to use. What are some good ways to check their functionality?

Bacterial contamination is the most common cause of microspheres becoming unusable. Many of our particles are supplied with a low level of sodium azide to prevent bacterial contamination, but sometimes this can still occur. Bacterial contamination is best assessed by plating on appropriate growth medium and checking the plates after 72 hr.

Find additional tips, troubleshooting help, and resources within ourMicrospheres Support Center.

I accidentally froze my microspheres; can I still use them?

Even brief freezing can cause irreversible aggregation and potential distortion of the bead shape. You should not use these microspheres.

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

인용 및 참조 문헌 (4)

인용 및 참조 문헌
Abstract
In vivo non-linear optical (NLO) imaging in live rabbit eyes using the Heidelberg Two-Photon Laser Ophthalmoscope.
Authors:Hao M, Flynn K, Nien-Shy C, Jester BE, Winkler M, Brown DJ, La Schiazza O, Bille J, Jester JV,
Journal:Exp Eye Res
PubMed ID:20558159
Imaging of non-linear optical (NLO) signals generated from the eye using ultrafast pulsed lasers has been limited to the study of ex vivo tissues because of the use of conventional microscopes with slow scan speeds. The purpose of this study was to evaluate the ability of a novel, high scan ... More
Accelerated phagocytosis of amyloid-beta by mouse and human microglia overexpressing the macrophage colony-stimulating factor receptor.
Authors:Mitrasinovic OM, Murphy GM Jr.
Journal:J Biol Chem
PubMed ID:12032144
Microglia surrounding A beta plaques in Alzheimer's disease and in the APPV717F transgenic mouse model of Alzheimer's disease have enhanced immunoreactivity for the macrophage colony-stimulating factor receptor (M-CSFR), encoded by the proto-oncogene c-fms. Increased expression of M-CSFR on cultured microglia results in proliferation and release of pro-inflammatory cytokines and expression ... More
Accurate and fiducial-marker-free correction for three-dimensional chromatic shift in biological fluorescence microscopy.
Authors:Matsuda A, Schermelleh L, Hirano Y, Haraguchi T, Hiraoka Y
Journal:Sci Rep
PubMed ID:29765093
'Correction of chromatic shift is necessary for precise registration of multicolor fluorescence images of biological specimens. New emerging technologies in fluorescence microscopy with increasing spatial resolution and penetration depth have prompted the need for more accurate methods to correct chromatic aberration. However, the amount of chromatic shift of the region ... More
Tissue Damage Signaling Is a Prerequisite for Protective Neutrophil Recruitment to Microbial Infection in Zebrafish.
Authors:Huang C, Niethammer P
Journal:Immunity
PubMed ID:29768163
Tissue damage and infection are deemed likewise triggers of innate immune responses. But whereas neutrophil responses to microbes are generally protective, neutrophil recruitment into damaged tissues without infection is deleterious. Why neutrophils respond to tissue damage and not just to microbes is unknown. Is it a flaw of the innate ... More