SlowFade™ Diamond Antifade Mountant with DAPI
SlowFade™ Diamond Antifade Mountant with DAPI
Invitrogen™

SlowFade™ Diamond Antifade Mountant with DAPI

SlowFade Diamond退色防止用封入剤は、グリセロールベースの液体封入剤であり、顕微鏡スライド上の蛍光標識細胞や組織サンプルに直接塗布します。可視および赤外スペクトル全域にわたって優れた褪色防止効果を発揮します。SlowFade Diamond封入剤は、ほぼすべての蛍光色素や蛍光タンパク質(GFP、RFP詳細を見る
製品番号(カタログ番号)容量(メートル法)
S3697310 mL
S369645 x 2 mL
S369682 mL
製品番号(カタログ番号) S36973
価格(JPY)
35,100
Each
お問い合わせください ›
容量(メートル法):
10 mL
SlowFade Diamond退色防止用封入剤は、グリセロールベースの液体封入剤であり、顕微鏡スライド上の蛍光標識細胞や組織サンプルに直接塗布します。可視および赤外スペクトル全域にわたって優れた褪色防止効果を発揮します。SlowFade Diamond封入剤は、ほぼすべての蛍光色素や蛍光タンパク質(GFP、RFP、mCherry など)と組み合わせることで、非常に輝度の高いシグナルと低いバックグラウンドを実現します。

SlowFade Diamond退色防止用封入剤には、以下の特長があります:
•可視および IR スペクトル全体にわたって、蛍光色素および蛍光タンパク質を退色から保護します
• すぐに使用可能な液体で硬化しないため、すぐにサンプルを観察することができます
• Alexa Fluor、FITCやCy3などの従来の色素、GFP、RFP、およびmCherryなどの蛍光タンパク質に最適です
• 蛍光シグナルの維持—ほとんど、またはまったく消光しません

蛍光イメージングのニーズに適した褪色防止用封入剤または光学洗浄試薬を選択 ›

高解像度、または厚みのある組織や3D細胞培養を焦点深度 0~500 µmでイメージングするには、 SlowFade Glass退色防止用封入剤をお試しください。屈折率1.52のRIMS封入剤です。

お客様の実験ニーズに最適な SlowFade退色防止用試薬をお選びください ›

SlowFade Diamond退色防止用封入剤は、すでにミックスされており、すぐに使用可能なドロッパーボトルで、DAPI含有タイプまたは不含タイプがあります。サンプルに一滴垂らしてカバースリップを載せ、イメージングするだけです。カバースリップの端を適切なカバースリップシール剤でシールすると、サンプルを数日から数週間保存できます。ガラスや液浸油に近い屈折率で長期保存する場合は、 ProLong Glass褪色防止用封入剤 をお勧めします。SlowFade Diamond封入剤の硬化を必要としない特性により、ラベリング後すぐにサンプルの評価およびイメージングができます。

可視およびIRスペクトルの全域にわたって光退色から保護します
どの蛍光色素や蛍光タンパク質を使用していても、SlowFade Diamond封入剤は光退色に対する最良の保護を提供します。最高クラスの性能は、Alexa Fluor色素、FITC、TRTC、Texasレッド、Cy3、Cy5 などの幅広い蛍光色素との組み合わせで実証されています。SlowFade Diamond封入剤は消光しません。また、バックグラウンドなしでより明るいシグナルを提供できるため、出版に最適な品質の高解像度画像を得ることができます。

イメージング中および迅速な確認のための安定したシグナル
SlowFade Diamond封入剤は、ラベリング直後のサンプル分析に最適なオプションです。蛍光色素や蛍光タンパク質に対する退色防止特性により、長時間のイメージングセッション中(共焦点レーザースキャン照明下でスキャンを繰り返す場合など)や超高解像度顕微鏡を使用するときに、シグナル強度を維持することができます。さらに、染色したサンプルやマウントから余分な水分を除去するだけという使いやすさも兼ね備えています。スライドシール剤を使用すると、スライドを数日間または数週間保存できます。より長いアーカイブが必要な場合は、SlowFade Diamond封入剤をPBS で洗浄し、ProLong Diamond退色防止用封入剤でサンプルを再マウントできます。

鮮明な画像を得るための優れた屈折率を実現
最新の高解像度イメージングアプリケーションにおいて、屈折率(RI)マッチングが不可欠です。SlowFade™ Diamond封入剤の屈折率は1.42で、培養細胞や組織の薄いスライスにお勧めです(厚さ10 μm未満)。
研究用にのみ使用できます。診断用には使用いただけません。
仕様
数量10 mL
出荷条件室温またはウェットアイスでの出荷
製品ラインSlowFade
製品タイプAntifade Mountant
試薬タイプ抗褪色溶液
容量(メートル法)10 mL
Unit SizeEach
組成および保存条件
10 mLボトル1本。
•2~8℃で保存するか、-20℃で凍結保存してください
• 光から保護してください
• 受け取り後6 ヶ月間は安定しています。

よくあるご質問(FAQ)

What is the difference between ProLong and SlowFade antifade reagents?

Our ProLong antifade reagents dispense as a liquid that will solidify upon the evaporation of water. SlowFade antifade reagents remain liquid. If you are going to image right away and then dispose of your sample, you do not need a mountant that hardens, such as the SlowFade reagents. If you wish to archive your slide for more than a day, you will want a mounting medium that hardens (or “cures”). This hardening will limit the off-rates of various dye-conjugated antibodies and provides a better refractive index. Also, there will be a lower diffusion rate of free radicals, limiting photobleaching.

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

Some antifade mounting media stay as liquid whereas others harden. What is the benefit of having one that hardens?

If you are going to image right away and then dispose of your sample, you probably want a mountant that does not harden. If you wish to archive your slide for more than a day, you want a mountant that hardens (or "cures"). This hardening will slow or prevent off-rate of your dye or conjugate and often produces a better refractive index. Secondary sealing is usually not necessary. Also there will be lower diffusion of free radicals, thus limiting photobleaching.

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.

Does Slowfade Antifade Mountant require using a nail polish for sealing?

No. Samples mounted with SlowFade mountants need not be sealed; they are intended for immediate viewing. The coverslip may be anchored (to prevent movement while viewing) by applying molten paraffin to three or four spots around the edge of the coverslip.

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

I want to mount my dye-labeled cells in an antifade mounting medium to keep the dyes from photobleaching. Which mounting medium do you recommend?

As dyes are illuminated for imaging, they will fade, or “photobleach”, leading to unwanted dimming and lower detection efficiency over time. An antifade mounting medium can greatly reduce photobleaching. If you wish to label live cells, use of ProLong Live Antifade Reagent is helpful. If you wish to mount fixed cells after labeling, and then image immediately and then discard, SlowFade Diamond Antifade Mountant stays liquid but has good refractive index. If you wish to mount your sample and then archive the slides, ProLong Diamond Antifade Mountant will harden to a better refractive index and allow for archiving of the sample for up to several weeks, or even months. Unlike other antifade mounting media, these work well with fluorescent proteins for immediate viewing (archiving fluorescent proteins is not possible), and they are packaged with or without DAPI. More information on these can be found here (https://www.thermofisher.com/us/en/home/life-science/cell-analysis/cellular-imaging/fluorescence-microscopy-and-immunofluorescence-if/mounting-medium-antifades/prolong-gold-antifade.html).

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

引用および参考文献 (17)

引用および参考文献
Abstract
Human Primordial Germ Cells Are Specified from Lineage-Primed Progenitors.
Authors:Chen D, Sun N, Hou L, Kim R, Faith J, Aslanyan M, Tao Y, Zheng Y, Fu J, Liu W, Kellis M, Clark A
Journal:Cell Rep
PubMed ID:31875561
'In vitro gametogenesis is the process of making germline cells from human pluripotent stem cells. The foundation of this model is the quality of the first progenitors called primordial germ cells (PGCs), which in vivo are specified during the peri-implantation window of human development. Here, we show that human PGC (hPGC) specification ... More
Fetal testis organ culture reproduces the dynamics of epigenetic reprogramming in rat gonocytes.
Authors:Rwigemera A, Joao F, Delbes G
Journal:Epigenetics Chromatin
PubMed ID:28413450
'Epigenetic reprogramming is a critical step in male germ cell development that occurs during perinatal life. It is characterized by the remodeling of different epigenetic marks such as DNA methylation (5mC) and methylation of histone H3. It has been suggested that endocrine disruptors can affect the male germline epigenome by ... More
Biphasic ROS production, p53 and BIK dictate the mode of cell death in response to DNA damage in colon cancer cells.
Authors:Kutuk O, Aytan N, Karakas B, Kurt AG, Acikbas U, Temel SG, Basaga H
Journal:PLoS One
PubMed ID:28796811
'Necrosis, apoptosis and autophagic cell death are the main cell death pathways in multicellular organisms, all with distinct and overlapping cellular and biochemical features. DNA damage may trigger different types of cell death in cancer cells but the molecular events governing the mode of cell death remain elusive. Here we ... More
Altered chromatin compaction and histone methylation drive non-additive gene expression in an interspecific Arabidopsis hybrid.
Authors:Zhu W, Hu B, Becker C, Dogan ES, Berendzen KW, Weigel D, Liu C
Journal:Genome Biol
PubMed ID:28830561
'The merging of two diverged genomes can result in hybrid offspring that phenotypically differ greatly from both parents. In plants, interspecific hybridization plays important roles in evolution and speciation. In addition, many agricultural and horticultural species are derived from interspecific hybridization. However, the detailed mechanisms responsible for non-additive phenotypic novelty ... More
SosA inhibits cell division in Staphylococcus aureus in response to DNA damage.
Authors:Bojer MS, Wacnik K, Kjelgaard P, Gallay C, Bottomley AL, Cohn MT, Lindahl G, Frees D, Veening JW, Foster SJ, Ingmer H
Journal:Mol Microbiol
PubMed ID:31290194
'Inhibition of cell division is critical for viability under DNA-damaging conditions. DNA damage induces the SOS response that in bacteria inhibits cell division while repairs are being made. In coccoids, such as the human pathogen, Staphylococcus aureus, this process remains poorly studied. Here, we identify SosA as the staphylococcal SOS-induced ... More