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Principaux documents

F6182

Sigma-Aldrich

Fluoroshield™

liquid

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About This Item

Code UNSPSC :
12171500
Nomenclature NACRES :
NA.47

Nom du produit

Fluoroshield™, histology mounting medium

Niveau de qualité

100

Forme

liquid

Technique(s)

immunofluorescence: suitable

Plage de pH

7.8-8.2

Solubilité

water: soluble

Application(s)

diagnostic assay manufacturing
hematology
histology

Température de stockage

2-8°C

Description générale

Fluoroshield is an aqueous mounting medium for preserving fluorescence of tissue and cell smears. This unique formula not only enables prolonged fluorescence, but also prevents rapid photobleaching (fading) of fluorochromes including FITC, Texas Red®, AMCA, Cy®, Cy3™, Cy5, Alexa Fluor™ 488, Alexa Fluor™ 594, Green fluorescent protein (GFP), tetramethylrhodamine, R-phycoerythrin (R-PE), phycocyanin (PC), and allophycocyanin (APC).

Application

Fluoroshield™ has been used:
  • as a mounting medium for cultured megakaryocytes and immunostained platelets for confocal microscopy studies
  • as a mounting medium for 4′,6-diamidino-2-phenylindole (DAPI) stained heart sections for immunofluorescence studies
  • to preserve fluorescence of C6 cell smears

Liaison

Fluoroshield is an aqueous-based mounting medium comparable to Gel Mount™.

Informations légales

ALEXA FLUOR is a trademark of Life Technologies
Cy is a registered trademark of Cytiva
Cy3 is a trademark of Cytiva
FluoroShield is a trademark of ImmunoBioScience Corp.
Gel Mount is a trademark of Biomeda Corp.
Texas Red is a registered trademark of Life Technologies

Produit(s) apparenté(s)

Réf. du produit
Description
Tarif

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

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Certificats d'analyse (COA)

Lot/Batch Number
MKCQ9296
MKCQ4438
MKCP9166
MKCP4948
MKCP0142

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

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Chenchen Yang et al.
Scientific reports, 8(1), 16359-16359 (2018-11-07)
Visibly transparent luminescent solar concentrators (TLSC) have the potential to turn existing infrastructures into net-zero-energy buildings. However, the reabsorption loss currently limits the device performance and scalability. This loss is typically defined by the Stokes shift between the absorption and
Effects of dexamethasone on C6 cell proliferation, migration and invasion through the upregulation of AQP1
Guan Y, et al.
Oncology Letters, 15(5), 7595-7602 (2018)
F Lodola et al.
Science advances, 5(9), eaav4620-eaav4620 (2019-10-11)
The control of stem and progenitor cell fate is emerging as a compelling urgency for regenerative medicine. Here, we propose a innovative strategy to gain optical control of endothelial colony-forming cell fate, which represents the only known truly endothelial precursor
Douglas H Campbell et al.
PloS one, 13(4), e0196017-e0196017 (2018-04-20)
While measurement of serum prostate specific antigen (PSA) is an important screening tool for prostate cancer, new biomarkers are necessary for better discrimination between presence and absence of disease. The MIL-38 monoclonal antibody is specific for the membrane glycoprotein glypican
Venugopal Thayanithy et al.
Cell communication and signaling : CCS, 15(1), 46-46 (2017-11-15)
Tunneling nanotubes (TNTs) are naturally-occurring filamentous actin-based membranous extensions that form across a wide spectrum of mammalian cell types to facilitate long-range intercellular communication. Valid assays are needed to accurately assess the downstream effects of TNT-mediated transfer of cellular signals
Afficher tous les articles scientifiques apparentés

Articles

Cell and Organelle Labeling with Fluorescent Antibodies

The Human Protein Atlas Program has carefully selected three different human cell lines, A-431 epidermoid carcinoma, U-251 MG glioblastoma and U-205 osteosarcoma, for organelle mapping of the proteome. As Prestige Antibodies are studied by immunofluorescence (IF) staining, three well-characterized organelle markers for nuclei, microtubules and endoplasmic reticulum are used correspondingly as specific probes. The high-resolution confocal images are annotated based on sub-cellular localization. In addition, staining intensity and characteristics are also part of an overall assessment as well as comparison to literature (if available).

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