ProLong™ Gold Antifade Mountant with DNA Stain DAPI
ProLong™ Gold Antifade Mountant with DNA Stain DAPI
ProLong™ Gold Antifade Mountant with DNA Stain DAPI
ProLong™ Gold Antifade Mountant with DNA Stain DAPI
Invitrogen™

ProLong™ Gold Antifade Mountant with DNA Stain DAPI

Green features
ProLong Diamond退色防止用封入剤は液体封入剤であり、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。DNA染色剤なし、または青色DNA染色剤のDAPI、または深紅色DNA染色剤のSYTOX Deep Redで構成されています。ProLong Gold封入剤には詳細を見る
製品番号(カタログ番号)数量
P369311 x 10 mL
P369411 x 2 mL
P369355 x 2 mL
製品番号(カタログ番号) P36931
価格(JPY)
41,200
Each
お問い合わせください ›
数量:
1 x 10 mL
ProLong Diamond退色防止用封入剤は液体封入剤であり、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。DNA染色剤なし、または青色DNA染色剤のDAPI、または深紅色DNA染色剤のSYTOX Deep Redで構成されています。ProLong Gold封入剤には、蛍光顕微鏡実験中に蛍光色素が退色(光退色)しないように設計された化学成分が含まれており、初期蛍光シグナルを大幅に消光することなく退色保護を実現します。ほぼ完璧な光学経路(1.47 RI)を形成する硬化封入剤で、サンプルの長期保存を可能にします。すぐに使用できます(室温保存で混合は不要)—サンプルに一滴添加し、カバースリップをかけて、硬化し、イメージングするだけです。

ProLong Gold退色防止用封入剤は、GFPなどの蛍光タンパク質を含むサンプルのマウントには推奨されていません。蛍光タンパク質および蛍光色素の優れた褪色防止効果を得るには、ProLong Diamond退色防止用封入剤をお勧めします。ProLong GoldとProLong Diamond褪色防止用封入剤の主な違いについては、こちらをご覧ください。

主な特性:

•イメージング中の色素の色あせを防止
• すぐに使用可能な液体で長期保存のために硬化します
• マウントされたサンプルは数ヶ月間間安定しています
• 蛍光シグナルを維持—ほとんど、またはまったく消光しません
• Alexa Fluor色素に最適

油浸漬対物イメージング用に最適化された屈折率1.52の封入剤には、硬化性封入剤である ProLong Glass退色防止用封入剤 または非硬化性の SlowFade Glassソフトセット退色防止用封入剤をお試しください。

ProLong Gold退色防止用封入剤は、すでに混合されており、DNA染色剤含有または不含の10 mLボトルで、使いやすいドロッパーボトルです。DAPI染色剤は、DNAに結合すると、UV光によって360 nmで励起され、460 nmで最大の発光を示し、DAPI従来のフィルターを使用して検出します。SYTOX Deep Red染色剤は、DNAに結合すると赤色光によって660 nmで励起され、682 nmで最大の発光を示し、Cy5/ディープレッドの従来型フィルターを使用して検出します。

消光することなく光退色防止を実現
多くの封入剤は、初期の蛍光シグナル強度を最大80%まで破壊する可能性があります。Molecular Probes Goldシリーズの封入剤を作製するために、当社の研究者は、幅広い色と色素に対応した初期シグナルの消光を最小限に抑える化学添加剤の組成を開発しました。

イメージング中および長期保存時に安定したシグナルを提供
当社の調製細胞FluoCellsシリーズで使用されるエポキシベースの封入剤は、長年安定しており、最高レベルの褪色防止効果を得ることができるものの、使用が困難で、取り付け前に有機溶媒での一連の手順が必要です。ProLong Gold退色防止用封入剤は、サンプルを保管するための二番目に最適なオプションです。また、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)にシグナル強度を維持するために最適な選択です。使いやすい—染色したサンプルを空気乾燥するだけで、過剰な水を除去してマウントすることができます。サンプルをすぐに確認するには、非硬化性封入剤である SlowFade Gold退色防止用封入剤をお選びください。

アクリル樹脂を使用しない優れた屈折率マッチングを実現
最新の高解像度イメージングアプリケーションでは、屈折率マッチングが重要です。ProLong Gold退色防止用封入剤の硬化後屈折率は1.47です。さらに、硬化特性はAVが可能であることを意味します
研究用途にのみご使用ください。診断目的には使用できません。
仕様
グリーン機能危険性の少ない、持続可能な包装
数量1 x 10 mL
出荷条件室温
製品ラインProLong
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
常温での保存をお勧めしますが、冷凍保存も可能です(-5~-30℃)。遮光。

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.

If I use ProLong Gold Antifade Mountant to mount my slides, should I seal the edges?

ProLong Gold Antifade Mountant hardens overnight at room temperature. For short-term storage (a couple of weeks) you do not need to seal the edges of the coverslip, and the sample should be stable. Beyond that time, though, some dye conjugates will have an off-rate into the medium, so cold storage is recommended. Sealing the edges will prevent long-term discoloration (golden color) from developing around the edges of the coverslip as the anti-oxidants oxidize.

The edges may be sealed with melted paraffin, VALAP (1:1:1 vaseline, lanolin, paraffin) or epoxy glue. Nail polish is not recommended as various components of nail polish may diffuse into the mountant and quench fluorescent dyes.

Find additional tips, troubleshooting help, and resources within our Cell Imaging 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 mounted my cells in ProLong antifade mounting medium, but now I want to go back and re-label them. Is there a way I can unmount the coverslip after it has cured (hardened)?

Yes. Put the slide in a Coplin jar or beaker filled with warm (37oC) PBS buffer and let it sit, no agitation is required. The hardened ProLong mountant will swell and may slide off or be easily dislodged. If cells are adherent to the coverslip, make certain the coverslip side containing the cell or tissue sample does not land face down in the container or become scratched upon handling. Remove the coverslip, wash a couple of times, and proceed with re-staining and re-mounting in new ProLong mountant.

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

I am using ProLong antifade mounting medium. Do I need to let it cure before imaging? Do I need to seal the edges of the coverslip?

You can image before it cures (hardens), and it will still slow photobleaching, but you have to let it cure overnight to get the best refractive index (resolution). There is no need to seal the edges. In fact, if you seal before it cures, it won't cure correctly. If you are archiving the slide for more than a month, though, seal the edges with resin, paraffin or VALAP (1:1:1 vaseline, lanolin, paraffin) after it cures or there may be slight discoloration along the edges over time.

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

引用および参考文献 (18)

引用および参考文献
Abstract
Resolution of de novo HIV production and trafficking in immature dendritic cells.
Authors:Turville SG, Aravantinou M, Stössel H, Romani N, Robbiani M,
Journal:Nat Methods
PubMed ID:18059278
'The challenge in observing de novo virus production in human immunodeficiency virus (HIV)-infected dendritic cells (DCs) is the lack of resolution between cytosolic immature and endocytic mature HIV gag protein. To track HIV production, we developed an infectious HIV construct bearing a diothiol-resistant tetracysteine motif (dTCM) at the C terminus ... More
Androgen induces expression of the multidrug resistance protein gene MRP4 in prostate cancer cells.
Authors:Cai C, Omwancha J, Hsieh CL, Shemshedini L
Journal:Prostate Cancer Prostatic Dis
PubMed ID:17003774
'Multidrug resistance-associated proteins (MRPs) may mediate multidrug resistance in tumor cells. Using a gene array analysis, we have identified MRP4 as an androgen receptor (AR)-regulated gene. Dihydrotestosterone induced MRP4 expression in both androgen-dependent and -independent LNCaP cells, whereas there was little detectable expression in PC-3 or normal prostate epithelial cells. ... More
H2AX phosphorylation within the G1 phase after UV irradiation depends on nucleotide excision repair and not DNA double-strand breaks.
Authors:Marti TM, Hefner E, Feeney L, Natale V, Cleaver JE
Journal:Proc Natl Acad Sci U S A
PubMed ID:16788066
'The variant histone H2AX is phosphorylated in response to UV irradiation of primary human fibroblasts in a complex fashion that is radically different from that commonly reported after DNA double-strand breaks. H2AX phosphorylation after exposure to ionizing radiation produces foci, which are detectable by immunofluorescence microscopy and have been adopted ... More
Rab11-family interacting proteins define spatially and temporally distinct regions within the dynamic Rab11a-dependent recycling system.
Authors:Baetz NW, Goldenring JR,
Journal:Mol Biol Cell
PubMed ID:23283983
'The Rab11-family interacting proteins (Rab11-FIPs) facilitate Rab11-dependent vesicle recycling. We hypothesized that Rab11-FIPs define discrete subdomains and carry out temporally distinct roles within the recycling system. We used live-cell deconvolution microscopy of HeLa cells expressing chimeric fluorescent Rab11-FIPs to examine Rab11-FIP localization, transferrin passage through Rab11-FIP-containing compartments, and overlap among ... More
High-efficiency labeling of sialylated glycoproteins on living cells.
Authors:Zeng Y, Ramya TN, Dirksen A, Dawson PE, Paulson JC,
Journal:Nat Methods
PubMed ID:19234450
We describe a simple method for efficiently labeling cell-surface sialic acid-containing glycans on living animal cells. The method uses mild periodate oxidation to generate an aldehyde on sialic acids, followed by aniline-catalyzed oxime ligation with a suitable tag. Aniline catalysis dramatically accelerates oxime ligation, allowing use of low concentrations of ... More