ProLong™ Glass Antifade Mountant with NucBlue™ Stain
ProLong™ Glass Antifade Mountant with NucBlue™ Stain
ProLong™ Glass Antifade Mountant with NucBlue™ Stain
ProLong™ Glass Antifade Mountant with NucBlue™ Stain
Invitrogen™

ProLong™ Glass Antifade Mountant with NucBlue™ Stain

ProLong Glass Antifade with NucBlue Stain is a ready-to-use hard-setting mounting media with a refractive index of 1.52 for high深入閱讀
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產品號碼Quantity
P369815 x 2 mL
P369832 mL
P3698510 mL
產品號碼 P36981
價格 (TWD)
11,780.00
Online offer
Ends: 31-Dec-2025
15,700.00
您節省 3,920.00 (25%)
Each
新增至購物車
Quantity:
5 x 2 mL
價格 (TWD)
11,780.00
Online offer
Ends: 31-Dec-2025
15,700.00
您節省 3,920.00 (25%)
Each
新增至購物車

ProLong Glass Antifade with NucBlue Stain is a ready-to-use hard-setting mounting media with a refractive index of 1.52 for high resolution microscopy imaging that contains the nuclear counterstain Hoechst 33342 to detect DNA. ProLong Glass Antifade Mountant with NucBlue Stain can be applied directly to fluorescently labeled cells or tissue samples on slides or coverslips. When bound to DNA, NucBlue (Hoechst 33342) is excited by UV light at 360 nm with an emission maximum at 460 nm and is detected using a DAPI traditional filter. ProLong Glass mountant has a refractive index (RI) of 1.52, similar to glass coverslips, compatible immersion oil, and oil-immersion microscope optics, which enables superior resolution and sensitivity. ProLong Glass mounting media is designed to provide unparalleled photobleach protection across the visible and near infra-red spectra. You can use ProLong Glass Antifade Mountant with NucBlue Stain with almost any fluorescent dye or fluorescent protein (e.g., GFP, RFP, mCherry) and with any cell/tissue sample up to 150 microns in thickness. With embedded nuclear DNA counterstain of NucBlue within the ProLong Glass mounting media, multiplexing is smooth and effortless.

ProLong Glass Antifade Mountant with NucBlue Stain is provided in a 2 mL dropper bottle or 10 mL bottle. After removing excess water, just simply apply a drop of mounting media to the sample, add a coverslip, cure, and image. ProLong Glass Mountant with NucBlue Stain minimizes optical refraction and spherical aberration in the optical path, which enables longer-term storage of your samples. ProLong Glass with NucBlue Stain mountant does not discolor or shrink when cured and stored long term and provides nuclear counterstaining directly in the mounting media for DNA detection.

Optimal refractive index for the brightest and sharpest images
The RI determines how much the path of light is bent, or refracted, when entering a material. In microscopy, refractive index differences between specimen and mounting medium should be minimized and can be reduced by using mountants with a higher RI such as ProLong Glass mountant. Depending on your sample type, thickness, imaging depth and/or staining reagents (e.g. fluorescent proteins or dyes) and whether you need a curing or non-curing mountant, choosing the right mounting media will impact image resolution and should be strongly considered for optimal experimental design. For example, when Prolong Glass Antifade Mountant (1.52 RI) is compared with a mounting medium with a refractive index of 1.47, the axial resolution is improved by 32% at a focal depth of 40 μm and 75% at a focal depth of 100 μm. The signal intensity and sensitivity of fluorophores is also improved as the focal depth increases within the sample. Prolong Glass is optimal for acquisition of Z-Stack, 3D, and 2D images of cells and tissue up to 150 μm while providing superior nuclear labeling of most cells and tissues alongside NucBlue stain to assess DNA with nuclear staining.

Prevent photobleaching across the visible and near-IR spectra
Compatible with almost all fluorescent dyes and fluorescent proteins, ProLong Glass Antifade Mountant with NucBlue provides superior protection against photobleaching. ProLong Glass mounting media does not quench fluorophores and provides high-resolution images with a wide array of fluorescent dyes, including Alexa Fluor, FITC, TRTC, Texas Red, Cy3, and Cy5 dyes while NucBlue for nuclear DNA staining is delivered within the mountant. ProLong Glass Antifade Mountant is an ideal reagent for archiving samples and for preserving signal strength during prolonged imaging sessions, such as repeated scanning under confocal laser scanning illumination or with super-resolution microscopy,

Glass mountants are recommended for all immersion oil imaging applications and for samples greater than 10 microns. ProLong Glass Antifade Mountant with NucBlue stain contains an optimized concentration of Hoechst 33342 stain, which provides superior nuclear labeling of DNA within most cells and tissues. However, specimens thicker than 30 μm can require optimization and longer incubations. For specimens thicker than 30 μm, consider pre-incubation with labeling reagents such as NucBlue Live ReadyProbes Reagent followed by mounting with ProLong Glass Antifade Mountant. To image your sample immediately after NucBlue staining, use our SlowFade Glass Antifade Mountant, a non-curing mountant with similar 1.52 refractive index properties.

For Research Use Only. Not for use in diagnostic procedures.
規格
DescriptionProLong™ Glass Antifade Mountant with NucBlue™ Stain, 5 x 2 mL
Quantity5 x 2 mL
Shipping ConditionApproved for shipment on Wet or Dry Ice
Product LineProLong
Product TypeAntifade Mountant
Reagent TypeAntifade Solution
Volume (Metric)2 mL
Unit SizeEach
內容物與存放
Store at 2°C to 8°C.

常見問答集 (常見問題)

I mounted my antibody-labeled brain cryosection in either ProLong Antifade Mountant, ProLong Gold, ProLong Diamond or ProLong Glass Antifade Mountant. It looked good when first mounted, but after curing, it had tiny bubbles all over the tissue under the coverslip. The sample was air-dried prior to mounting. What happened and what can be done to remove the bubbles?

The tissue likely had air trapped in it, either before the labeling process or as a result of air-drying. While the tissue is in blocking solution or another wash, we recommend putting it in a vacuum to pull out internalized air. Air-drying is not necessary; just tap off excess buffer and mount the damp tissue with the mountant.

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

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.

What do ProLong Gold, ProLong Diamond and ProLong Glass antifade mountant reagents contain?

They are composed of proprietary antifades and polymers in aqueous buffers.

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

Can I use ProLong Gold, ProLong Diamond, or ProLong Glass mounting medium in a multi-well plate?

No. If the sample cannot be sealed with a coverslip, we recommend the use of SlowFade antifade mountant.

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

What can affect sample curing of ProLong Gold-, ProLong Diamond-, and ProLong Glass-mounted samples?

Our ProLong Gold, ProLong Diamond, and ProLong Glass mounting media harden ('cure') by the evaporation of water. Placing the mounted samples in a humid or refrigerated environment would slow down the evaporation process ('curing').

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

引用資料與參考文獻 (34)

引用資料與參考文獻
Abstract
Light Affects Mood and Learning through Distinct Retina-Brain Pathways.
Authors:Fernandez DC, Fogerson PM, Lazzerini Ospri L, Thomsen MB, Layne RM, Severin D, Zhan J, Singer JH, Kirkwood A, Zhao H, Berson DM, Hattar S
Journal:Cell
PubMed ID:30173913
Light exerts a range of powerful biological effects beyond image vision, including mood and learning regulation. While the source of photic information affecting mood and cognitive functions is well established, viz. intrinsically photosensitive retinal ganglion cells (ipRGCs), the central mediators are unknown. Here we reveal that the direct effects of ... More
Comprehensive structure and functional adaptations of the yeast nuclear pore complex.
Authors:Akey CW, Singh D, Ouch C, Echeverria I, Nudelman I, Varberg JM, Yu Z, Fang F, Shi Y, Wang J, Salzberg D, Song K, Xu C, Gumbart JC, Suslov S, Unruh J, Jaspersen SL, Chait BT, Sali A, Fernandez-Martinez J, Ludtke SJ, Villa E, Rout MP
Journal:Cell
PubMed ID:34982960
Nuclear pore complexes (NPCs) mediate the nucleocytoplasmic transport of macromolecules. Here we provide a structure of the isolated yeast NPC in which the inner ring is resolved by cryo-EM at sub-nanometer resolution to show how flexible connectors tie together different structural and functional layers. These connectors may be targets for ... More
Obesity Shapes Metabolism in the Tumor Microenvironment to Suppress Anti-Tumor Immunity.
Authors:Ringel AE, Drijvers JM, Baker GJ, Catozzi A, García-Cañaveras JC, Gassaway BM, Miller BC, Juneja VR, Nguyen TH, Joshi S, Yao CH, Yoon H, Sage PT, LaFleur MW, Trombley JD, Jacobson CA, Maliga Z, Gygi SP, Sorger PK, Rabinowitz JD, Sharpe AH, Haigis MC
Journal:Cell
PubMed ID:33301708
Obesity is a major cancer risk factor, but how differences in systemic metabolism change the tumor microenvironment (TME) and impact anti-tumor immunity is not understood. Here, we demonstrate that high-fat diet (HFD)-induced obesity impairs CD8(+) T cell function in the murine TME, accelerating tumor growth. We generate a single-cell resolution ... More
Pathogenic ubiquitination of GSDMB inhibits NK cell bactericidal functions.
Authors:Hansen JM, de Jong MF, Wu Q, Zhang LS, Heisler DB, Alto LT, Alto NM
Journal:Cell
PubMed ID:34022140
Gasdermin B (GSDMB) belongs to a large family of pore forming cytolysins that execute inflammatory cell death programs. While genetic studies have linked GSDMB polymorphisms to human disease, its function in the immunological response to pathogens remains poorly understood. Here, we report a dynamic host-pathogen conflict between GSDMB and the ... More
WNK kinases sense molecular crowding and rescue cell volume via phase separation.
Authors:Boyd-Shiwarski CR, Shiwarski DJ, Griffiths SE, Beacham RT, Norrell L, Morrison DE, Wang J, Mann J, Tennant W, Anderson EN, Franks J, Calderon M, Connolly KA, Cheema MU, Weaver CJ, Nkashama LJ, Weckerly CC, Querry KE, Pandey UB, Donnelly CJ, Sun D, Rodan AR, Subramanya AR
Journal:Cell
PubMed ID:36318922
When challenged by hypertonicity, dehydrated cells must recover their volume to survive. This process requires the phosphorylation-dependent regulation of SLC12 cation chloride transporters by WNK kinases, but how these kinases are activated by cell shrinkage remains unknown. Within seconds of cell exposure to hypertonicity, WNK1 concentrates into membraneless condensates, initiating ... More