SlowFade™ Glass Soft-Set Antifade Mountant
SlowFade™ Glass Soft-Set Antifade Mountant
Invitrogen™

SlowFade™ Glass Soft-Set Antifade Mountant

SlowFade Glass Antifade Mountant is a glycerol-based, ready-to-use, non-curing mountant applied directly to fluorescently labeled cell or tissue samples onRead more
Have Questions?
Change viewbuttonViewtableView
Catalog NumberVolume (Metric)
S36917-5X2ML5 x 2 mL
S369172 mL
Catalog number S36917-5X2ML
Price (USD)
-
Volume (Metric):
5 x 2 mL

SlowFade Glass Antifade Mountant is a glycerol-based, ready-to-use, non-curing mountant applied directly to fluorescently labeled cell or tissue samples on microscope slides. It is formulated to have a refractive index of 1.52 for sharper images and antifade components to resist photobleaching. The result is sharp, bright images with almost any fluorophore, with wide-field, confocal, or super-resolution microscopes, at focal depths of 0–500 μm.

Since SlowFade Glass Antifade Mountant is non-curing, cells can be imaged immediately after mounting, without any of the adverse effects on cell morphology that a curing mountant might cause. It comes ready to use—just apply a drop to the sample, add a coverslip, and image. It is available with or without DAPI nuclear stain.

If a curing, hard-set mountant is needed, also with a refractive index of 1.52, for years of slide storage, then Prolong Glass Antifade Mountant is recommended.

Features of SlowFade Glass Antifade Mountant include:
• Ready-to-use, glycerol-based, non-curing antifade mountant
• Refractive index of 1.52, with minimized spherical aberrations
• Up to three times better axial resolution compared to regular mountant
• Visible tissue optical clearing, even in sections up to 1-mm thick
• Sharp, bright images at any focal depth from 0 to 500 μm

Sharp images for deep 3D imaging
SlowFade Glass Antifade Mountant features a refractive index of 1.52 (similar to glass coverslips), with superior photobleach protection. It is compatible with immersion oil and oil-immersion microscope optics, enabling a refraction-free light path and minimized spherical aberration, which improves axial resolution by three times (at 150-μm focal depth) as measured by point spread function. When 1-mm thick tissue sections are mounted, there is visible optical tissue clearing, enabling deep 3D imaging. For 3D imaging of whole organs (up to 10 mm), please see Clearing Reagents for Imaging 3D Cell Culture and Tissue.

Inhibit photobleaching across the visible and near-IR spectra
No matter which fluorescent dyes or fluorescent proteins you are using, Slowfade Glass Antifade Mountant helps provide superior protection against photobleaching. It has been shown to have best-in-class performance with a wide array of fluorescent dyes, including Alexa Fluor, FITC, TRTC, Texas Red, Cy3, and Cy5 dyes, and fluorescent proteins, including GFP, RFP, and mCherry. SlowFade Glass mountant does not quench fluorophores, and its ability to provide brighter signal against no background helps ensure that you get the best-quality high-resolution images for publishing.

Non-curing mountant which does not expand or shrink specimens
Most tissue clearing techniques either expand or shrink the specimens, causing artifacts in specimen morphology. SlowFade Glass Antifade Mountant is non-curing and does not cause expansion or contraction of specimens, which we have verified using Hela spheroids and rat brain sections. This characteristic allows 3D imaging of truly native specimen morphology. The specimens are available for imaging immediately after mounting, and properly sealed slides can be stored for weeks or months for excellent

For Research Use Only. Not for use in diagnostic procedures.
Specifications
Quantity5 x 2 mL
Shipping ConditionApproved for shipment on Wet or Dry Ice
Product LineSlowFade
Product TypeAntifade Mountant
Reagent TypeAntifade Solution
Volume (Metric)5 x 2 mL
Unit SizeEach
Contents & Storage
Contains 5 dropper bottles containing 2 mL reagent each

Frequently asked questions (FAQs)

I do not have epoxy or VALAP to seal the coverslip. Do you offer an alternative coverslip sealant?

We offer ProLong Coverslip Sealant (Cat. No. P56128) that can be used to seal the edges of the coverslip and is compatible with both curing and non-curing mountant. The sealant is easy to apply and is brushed on after the mountant has cured, for long preservation of slides. The product page can be found here.

When using a hard-curing mountant, such as ProLong Antifade Mountant, make sure the mountant is fully cured before applying ProLong Coverslip Sealant. Since this sealant can seal moisture under the coverslip, it can interfere with the curing process.

When using a non-curing mountant, such as SlowFade Antifade Mountants, sealing can take place immediately after mounting.

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

Citations & References (5)

Citations & References
Abstract
The cytokine MIF controls daily rhythms of symbiont nutrition in an animal-bacterial association.
Authors:Koch EJ, Bongrand C, Bennett BD, Lawhorn S, Moriano-Gutierrez S, Pende M, Vadiwala K, Dodt HU, Raible F, Goldman W, Ruby EG, McFall-Ngai M
Journal:Proc Natl Acad Sci U S A
PubMed ID:33067391
'The recent recognition that many symbioses exhibit daily rhythms has encouraged research into the partner dialogue that drives these biological oscillations. Here we characterized the pivotal role of the versatile cytokine macrophage migration inhibitory factor (MIF) in regulating a metabolic rhythm in the model light-organ symbiosis between' ... More
4'-C-Trifluoromethyl modified oligodeoxynucleotides: synthesis, biochemical studies, and cellular uptake properties.
Authors:Zhou Y, Zang C, Wang H, Li J, Cui Z, Li Q, Guo F, Yan Z, Wen X, Xi Z, Zhou C
Journal:Org Biomol Chem
PubMed ID:31112186
Herein, we report the synthesis of 4'-C-trifluoromethyl (4'-CF3) thymidine (T4'-CF3) and its incorporation into oligodeoxynucleotides (ODNs) through solid-supported DNA synthesis. The 4'-CF3 modification leads to a marginal effect on the deoxyribose conformation and a local helical structure perturbation for ODN/RNA duplexes. This type of modification slightly decreases the thermal stability ... More
Epigenetic modulation of the MAPK pathway prevents isoflurane-induced neuronal apoptosis and cognitive decline in aged rats.
Authors:Huang L, Fang HB, Cheng HH, Mei SL, Cheng YP, Lv Y, Meng QT, Xia ZY
Journal:Exp Ther Med
PubMed ID:32952626
Isoflurane is a broadly used inhalation anesthetic that causes cognitive impairment in rodent models as well as humans. Although previous studies suggested an association between isoflurane exposure and neuro-inflammation, apoptosis and mitochondrial dysfunction, the pathogenesis of isoflurane-induced cognitive decline remains elusive. In the present study, 22-month-old male Sprague-Dawley male rats ... More
Real-time imaging of polymersome nanoparticles in zebrafish embryos engrafted with melanoma cancer cells: Localization, toxicity and treatment analysis.
Authors:Kocere A, Resseguier J, Wohlmann J, Skjeldal FM, Khan S, Speth M, Dal NK, Ng MYW, Alonso-Rodriguez N, Scarpa E, Rizzello L, Battaglia G, Griffiths G, Fenaroli F
Journal:EBioMedicine
PubMed ID:32707448
The developing zebrafish is an emerging tool in nanomedicine, allowing non-invasive live imaging of the whole animal at higher resolution than is possible in the more commonly used mouse models. In addition, several transgenic fish lines are available endowed with selected cell types expressing fluorescent proteins; this allows nanoparticles to ... More
The histone demethylase KDM5 is required for synaptic structure and function at the Drosophila neuromuscular junction.
Authors:Belalcazar HM, Hendricks EL, Zamurrad S, Liebl FLW, Secombe J
Journal:Cell Rep
PubMed ID:33596422
Mutations in the genes encoding the lysine demethylase 5 (KDM5) family of histone demethylases are observed in individuals with intellectual disability (ID). Despite clear evidence linking KDM5 function to neurodevelopmental pathways, how this family of proteins impacts transcriptional programs to mediate synaptic structure and activity remains unclear. Using the Drosophila ... More