FocalCheck™ Microspheres, 15 μm, fluorescent green ring stain/dark red throughout
FocalCheck™ Microspheres, 15 μm, fluorescent green ring stain/dark red throughout
Citations & References (2)
Invitrogen™

FocalCheck™ Microspheres, 15 μm, fluorescent green ring stain/dark red throughout

The sharp ring stains exhibited by the 15 μm FocalCheck™ fluorescent green ring stained/dark red throughout microspheres produce a strikingRead more
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Catalog NumberQuantity
F7238
also known as F-7238
0.5 mL
Catalog number F7238
also known as F-7238
Price (MXN)
-
Quantity:
0.5 mL
The sharp ring stains exhibited by the 15 μm FocalCheck™ fluorescent green ring stained/dark red throughout microspheres produce a striking visual representation of instrument misalignment or other aberrations making them ideal as reference standards for confocal laser-scanning microscopy. Correct image registration is indicated when the ring image and disk image of the combination beads are perfectly coincident in all dimensions.

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For Research Use Only. Not for use in diagnostic procedures.
Specifications
Calibration TypeConfocal Microscope Calibration
FormatSuspension Beads
Product LineFocalCheck
Quantity0.5 mL
Shipping ConditionRoom Temperature
ColorDark Red, Green
Diameter (Metric)15 μm
Product TypeMicrosphere
Unit SizeEach
Contents & Storage
Store in refrigerator 2°C to 8°C and protect from light.

Citations & References (2)

Citations & References
Abstract
Targeting of U2AF65 to sites of active splicing in the nucleus.
Authors:Gama-Carvalho M, Krauss RD, Chiang L, Valcárcel J, Green MR, Carmo-Fonseca M
Journal:J Cell Biol
PubMed ID:9166400
U2AF65 is an essential splicing factor that promotes binding of U2 small nuclear (sn)RNP at the pre-mRNA branchpoint. Here we describe a novel monoclonal antibody that reacts specifically with U2AF65. Using this antibody, we show that U2AF65 is diffusely distributed in the nucleoplasm with additional concentration in nuclear speckles, which ... More
Flexible Multi-Beam Light-Sheet Fluorescence Microscope for Live Imaging Without Striping Artifacts.
Authors:Sancataldo G, Gavryusev V, de Vito G, Turrini L, Locatelli M, Fornetto C, Tiso N, Vanzi F, Silvestri L, Pavone FS
Journal:Front Neuroanat
PubMed ID:30800060
The development of light-sheet fluorescence microscopy (LSFM) has greatly expanded the experimental capabilities in many biological and biomedical research fields, enabling for example live studies of murine and zebrafish neural activity or of cell growth and division. The key feature of the method is the selective illumination of a sample ... More