LIVE/DEAD™ Fixable Yellow Dead Cell Stain Kit, for 405 nm excitation
LIVE/DEAD™ Fixable Yellow Dead Cell Stain Kit, for 405 nm excitation
Invitrogen™

LIVE/DEAD™ Fixable Yellow Dead Cell Stain Kit, for 405 nm excitation

LIVE/DEAD™ Fixable Yellow Dead Cell Stain Kitは、細胞内抗体染色に必要な固定および透過の前、またはホルムアルデヒド固定を使用した生物学的有害物質の除去の前に、細胞の生存率を測定するために使用します詳細を見る
製品番号(カタログ番号)数量
L34967
または、製品番号L-34967
80アッセイ
L34959200アッセイ
L34968400 Assays
製品番号(カタログ番号) L34967
または、製品番号L-34967
価格(JPY)
37,400
Each
お問い合わせください ›
数量:
80アッセイ
LIVE/DEAD™ Fixable Yellow Dead Cell Stain Kitは、細胞内抗体染色に必要な固定および透過の前、またはホルムアルデヒド固定を使用した生物学的有害物質の除去の前に、細胞の生存率を測定するために使用します。このキットはバイオレットレーザーフローサイトメーターで使用するように最適化および検証されています。

•安定—色素は別々のバイアルに凍結乾燥されているため安定性を維持

• 堅牢—染色パターンは固定の前後で同じ

• 低補正—他の蛍光色素とのスペクトルオーバーラップが最小

フローサイトメトリー用の固定可能なすべての生存性色素の選択ガイドを見る。

安定
LIVE/DEAD™ Fixable Yellow Stainは溶液で販売される製品とは異なり、40本の試験バイアルに便利に包装されているため、色素の安定性と性能を長期間確保します。溶液中のアミン反応性色素は短時間で有効性を失います。そのため、再水和した後はバイアルを完全に使い切ることが推奨されます。これが不可能な場合は、バイアルを少量ずつ分注して-80℃で保存し、凍結融解の繰り返しを避けます。

堅牢
死細胞識別染色剤は、細胞内リン酸化研究に必要な、ホルムアルデヒドなどの固定剤やエタノールベースの固定法による処理後に感度が低下する可能性があります。LIVE/DEAD™ Fixable Yellow Stainは、細胞内および細胞外のアミンと共有結合するアミン反応性色素で、染色パターンはホルムアルデヒドによる固定後も維持されます。

低補正
LIVE/DEAD™ Fixable Yellow Stainは、他のバイオレット色素や488 nm青色レーザーから励起する色素との補正を最小限に抑えるよう、その蛍光特性に基づいて選択されています。黄色蛍光反応性色素の最大励起波長は約405 nmですが、405 nmバイオレットレーザーで良好に励起し、最大発光波長は約570 nmです。そのため、ほとんどのバイオレットレーザーフローサイトメーターの第2または第3チャンネルで捕獲できます。

原理
細胞膜が損傷した細胞において、この色素は細胞内および細胞表面の遊離アミンと反応して強い蛍光染色を生じます。生細胞では、色素の反応性は細胞表面のアミンに限定されるため、蛍光の強度は低下します。強度の差は通常、生細胞と死細胞の間で50倍を超えるため、容易に識別できます。

利用可能な色
LIVE/DEAD™ Fixable Dead Cell Stainはお客様のマルチカラーパネルのニーズを満たすよう、さまざまな色で提供されています。
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
細胞透過性Impermeant
細胞タイプ真核細胞
概要LIVE/DEAD™ Fixable Yellow Dead Cell Stain Kit, for 405 nm excitation
検出法蛍光
染色剤タイプLIVE/DEAD™ Fixable Yellow Dead Cell Stain
形状固体
フォーマットチューブ
数量80アッセイ
出荷条件室温
溶解性DMSO(ジメチルスルホキシド)
Yellow
Emission405/575
Excitation Wavelength Range405 nm
使用対象(アプリケーション)生存率アッセイ
使用対象 (装置)フローサイトメーター
製品ラインLIVE/DEAD
製品タイプ染色
Unit SizeEach
組成および保存条件
LIVE/DEAD™固定可能な死細胞染色液 x 2バイアル、500 μL DMSO。-20℃で保存

よくあるご質問(FAQ)

How long can I store LIVE/DEAD Fixable Yellow Dead Cell Stain Kit, for 405 nm excitation (Cat. No. L34959) at -20 degrees C?

Once reconstituted, the Live/Dead fixable dyes are guaranteed to be stable at -20 degrees C for a few weeks. We have not tested storage conditions beyond this time frame. The dye breaks down in water so the condition of the DMSO that is used for resuspension is the most important determinant.

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

How do I prepare dead cell controls for LIVE/DEAD cell viability assays?

There are two easy options. One is to heat-inactivate the cells by placing at 60 degrees C for 20 minutes. The second is to subject the cells to 70% ethanol. Alcohol-fixed cells can be stored indefinitely in the freezer until use, potentially up to several years.

Centrifuge cells, pellet, and remove supernatant.
Fix cells: Add 10 mL ice cold 70% ETOH to a 15 mL tube containing the cell pellet, adding dropwise at first while vortexing, mix well.
Store in freezer until use.
When ready to use, wash twice and resuspend in buffer of choice.

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

Which cell viability kits are compatible with fixation?

The LIVE/DEAD Fixable kits for flow cytometry analysis are compatible with fixation. These kits use amine-reactive cell-impermeant dyes that stain the cell surface of live cells and also the cytosol of dead cells-live cells are dim and dead cells are bright. Since the dye is covalently bound to the cells, it will be retained after fixation. Unfortunately, this method does not work well for imaging-based assays, as all cells are stained and it is difficult to distinguish bright dead cells from dim live cells with a microscope. Ethidium monoazide (EMA; Cat No. E1374) is a cell impermeant nucleic acid stain that can be applied to live cultures and stains only dead cells. After incubation and washing away unbound dye, the cells can be exposed to light to photoactivate EMA to crosslink to dead cell DNA. After crosslinking to dead cell DNA, the samples may be fixed and permeabilized. Image-IT DEAD Green Viability Stain (Cat. No. I10291) for imaging and high-content screening (HCS) analysis is a live-cell impermeant DNA binding dye that is compatible with fixation and permeabilization with good retention up to 48 hours. We also have a LIVE/DEAD Reduced Biohazard Cell Viability Kit (Cat. No. L7013) for imaging and flow analysis that contains two DNA binding dyes, SYTO 10 and Dead Red, that are sufficiently retained to be analyzed soon after 4% glutaraldehyde fixation.
Note: In general, DNA-binding dyes and calcein AM are not compatible with fixation, as these dyes are not covalently bound to components of the cell and will thus slowly diffuse out of cells after fixation, gradually staining all cells as dead.

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

引用および参考文献 (13)

引用および参考文献
Abstract
Tadalafil reduces myeloid-derived suppressor cells and regulatory T cells and promotes tumor immunity in patients with head and neck squamous cell carcinoma.
Authors:Weed DT, Vella JL, Reis IM, De la Fuente AC, Gomez C, Sargi Z, Nazarian R, Califano J, Borrello I, Serafini P,
Journal:
PubMed ID:25320361
Myeloid-derived suppressor cells (MDSC) and regulatory T cells (Treg) play a key role in the progression of head and neck squamous cell carcinoma (HNSCC). On the basis of our preclinical data demonstrating that phosphodiesterase-5 (PDE5) inhibition can modulate these cell populations, we evaluated whether the PDE5 inhibitor tadalafil can revert ... More
Influenza A and methicillin-resistant Staphylococcus aureus co-infection in rhesus macaques - A model of severe pneumonia.
Authors:Chertow DS, Kindrachuk J, Sheng ZM, Pujanauski LM, Cooper K, Nogee D, Claire MS, Solomon J, Perry D, Sayre P, Janosko KB, Lackemeyer MG, Bohannon JK, Kash JC, Jahrling PB, Taubenberger JK,
Journal:Antiviral Res
PubMed ID:26923881
'Influenza results in up to 500,000 deaths annually. Seasonal influenza vaccines have an estimated 60% effectiveness, but provide little or no protection against novel subtypes, and may be less protective in high-risk groups. Neuraminidase inhibitors are recommended for the treatment of severe influenza infection, but are not proven to reduce ... More
Treatment with retinoid X receptor agonist IRX4204 ameliorates experimental autoimmune encephalomyelitis.
Authors:Chandraratna RA, Noelle RJ, Nowak EC,
Journal:Am J Transl Res
PubMed ID:27158387
'Retinoid x receptors (RXRs) are master regulators that control cell growth, differentiation, and survival and form heterodimers with many other family members. Here we show that treatment with the RXR agonist IRX4204 enhances the differentiation of CD4(+) T cells into inducible regulatory T cells (iTreg) and suppresses the development of ... More
A tractable, simplified ex vivo human skin model of wound infection.
Authors:Yoon DJ, Fregoso DR, Nguyen D, Chen V, Strbo N, Fuentes JJ, Tomic-Canic M, Crawford R, Pastar I, Isseroff RR,
Journal:Wound Repair Regen
PubMed ID:30825247
'The prevalence of infection in chronic wounds is well documented in the literature but not optimally studied due to the drawbacks of current methodologies. Here, we describe a tractable and simplified ex vivo human skin model of infection that addresses the critical drawbacks of high costs and limited translatability. Wounds ... More
Targeting Hypoxia-Induced Carbonic Anhydrase IX Enhances Immune-Checkpoint Blockade Locally and Systemically.
Authors:Chafe SC, McDonald PC, Saberi S, Nemirovsky O, Venkateswaran G, Burugu S, Gao D, Delaidelli A, Kyle AH, Baker JHE, Gillespie JA, Bashashati A, Minchinton AI, Zhou Y, Shah SP, Dedhar S,
Journal:Cancer Immunol Res
PubMed ID:31088846
'Treatment strategies involving immune-checkpoint blockade (ICB) have significantly improved survival for a subset of patients across a broad spectrum of advanced solid cancers. Despite this, considerable room for improving response rates remains. The tumor microenvironment (TME) is a hurdle to immune function, as the altered metabolism-related acidic microenvironment of solid ... More