LIVE/DEAD™ Cell Vitality Assay Kit, C12 Resazurin/SYTOX™ Green
LIVE/DEAD&trade; Cell Vitality Assay Kit, C<sub>12</sub> Resazurin/SYTOX&trade; Green
Invitrogen™

LIVE/DEAD™ Cell Vitality Assay Kit, C12 Resazurin/SYTOX™ Green

LIVE/DEAD細胞生存率アッセイキットは、損傷細胞や死細胞と代謝活性細胞を区別するシンプルな2色の蛍光アッセイを提供します。このアッセイは、代謝活性細胞におけるC12-レサズリンから赤色蛍光のC12-レゾルフィンへの還元、および細胞膜が損なわれた細胞(通常は後期アポトーシス細胞および壊死細胞)における細胞不透過性の緑色蛍光核酸染色、SYTOX Green色素の取り込みに基づいています。このアッセイでは詳細を見る
製品番号(カタログ番号)数量
L349511,000
製品番号(カタログ番号) L34951
価格(JPY)
93,200
Each
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数量:
1,000
LIVE/DEAD細胞生存率アッセイキットは、損傷細胞や死細胞と代謝活性細胞を区別するシンプルな2色の蛍光アッセイを提供します。このアッセイは、代謝活性細胞におけるC12-レサズリンから赤色蛍光のC12-レゾルフィンへの還元、および細胞膜が損なわれた細胞(通常は後期アポトーシス細胞および壊死細胞)における細胞不透過性の緑色蛍光核酸染色、SYTOX Green色素の取り込みに基づいています。このアッセイでは、死細胞は主に緑色で蛍光発光し、健康で代謝活性のあるほとんどの細胞は赤色で蛍光発光します。損傷した細胞は、発光強度が低い赤色と緑色で蛍光発光します。

フローサイトメトリーに対応したすべての細胞生存率アッセイの選択ガイドをご覧ください。
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, Permeant
細胞タイプ哺乳類細胞、真核細胞
概要LIVE/DEAD™ Cell Vitality Assay Kit, C12 Resazurin/SYTOX™ Green
検出法蛍光
染色剤タイプその他の標識または色素
フォーマットチューブ
数量1,000
出荷条件室温
溶解性DMSO(ジメチルスルホキシド)
Green, Red
EmissionC12レサズリン:563⁄587、SYTOX™ Green 504⁄523
Excitation Wavelength Range504/563 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)蛍光顕微鏡, フローサイトメーター, マイクロプレートリーダー
製品ラインLIVE/DEAD、SYTOX
製品タイプCell Vitality Assay Kit
Unit SizeEach
組成および保存条件
C12-レサズリン(バイアル1本あたり40 μg)のバイアル5本、SYTOX™ Green(100 μL、DMSO溶液中に10 μM)のバイアル1本、DMSO(1.5 mL)のバイアル1本、および10Xリン酸バッファー(100 mL)入りです。 (フリーザー(-5℃~-30℃)に保存およびp

よくあるご質問(FAQ)

How do SYTO dyes bind to DNA?

The binding mode of SYTO nucleic acid stains is unknown. However, the behavior of these and related nucleic acid dyes suggests the following binding properties:

1.They appear to contact the solvent (suggested by sensitivity to salt, divalent cations, and in particular, SDS) and thus are likely to have contacts in the grooves.
2.All SYTO dyes appear to show some base selectivity and are thus likely to have minor groove contacts.
3.They can be removed from nucleic acid via ethanol precipitation; this characteristic is not shared by ethidium bromide and other intercalators. Likewise, the dyes are not removed from nucleic acid via butanol or chloroform extraction. These extraction methods do remove ethidium bromide from nucleic acid. 4. SYTO binding is not affected by nonionic detergents.
5. SYTO dyes are not quenched by BrdU, so they do not bind nucleic acids in precisely the same way as Hoechst 33342 and DAPI ((4′,6-diamidino-2-phenylindole).

SYBR Green I has shown little mutagenicity on frameshift indicator strains, indicating that it isn't likely to strongly intercalate.

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

How do alamarBlue reagent and PrestoBlue reagent differ from resazurin and C12-resazurin?

alamarBlue reagent and PrestoBlue reagent contain resazurin in a proprietary stabilizing formulation that allows for a convenient “mix, incubate, and read” protocol. PrestoBlue reagent is an improvement in the formulation of alamarBlue reagent that allows for much faster staining (typically 10 minutes vs. 1-4 hours to obtain a similar signal and sensitivity). C12-resazurin is a derivative of resazurin that has better cellular retention and thus allows for analysis on a flow cytometer and multiplexing with viability indicators and other biomarkers.

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.

引用および参考文献 (4)

引用および参考文献
Abstract
Titanium-Enriched Hydroxyapatite-Gelatin Scaffolds with Osteogenically Differentiated Progenitor Cell Aggregates for Calvaria Bone Regeneration.
Authors:Ferreira JR, Padilla R, Urkasemsin G, Yoon K, Goeckner K, Hu WS, Ko CC,
Journal:Tissue Eng Part A
PubMed ID:23495972
'Adequate bony support is the key to re-establish both function and esthetics in the craniofacial region. Autologous bone grafting has been the gold standard for regeneration of problematic large bone defects. However, poor graft availability and donor-site complications have led to alternative bone tissue-engineering approaches combining osteoinductive biomaterials and three-dimensional ... More
Local phagocytic responses after murine infection with different forms of Fonsecaea pedrosoi and sclerotic bodies originating from an inoculum of conidiogenous cells.
Authors:Machado AP, Silva MR, Fischman O,
Journal:Mycoses
PubMed ID:19925569
'Fonsecaea pedrosoi is an important causative agent of chromoblastomycosis (CBM) especially in humid areas of the world; however, little is known about the infective forms of this agent that cause CBM. The aim of this study was to investigate the murine tissue response to inoculation with different forms of F. ... More
Prolonged infection by Fonsecaea pedrosoi after antigenic co-stimulation at different sites in experimental murine chromoblastomycosis.
Authors:Machado AP, Silva MR, Fischman O,
Journal:Virulence
PubMed ID:21178410
'In the present study, we examined prolonged infection after antigenic co-stimulation by inoculation of the fungus Fonsecaea pedrosoi at two different sites in three mouse strains (BALB/c, Swiss, and C57BL/6). Using this murine model of infection, we showed that antigen induction of infection at more than one site led to ... More
Radio frequency radiation causes no nonthermal damage in enzymes and living cells.
Authors:Fortune JA, Wu BI, Klibanov AM,
Journal:Biotechnol Prog
PubMed ID:20572294
The ability of radio frequency radiation (RFR) to exert irreversible nonthermal (i.e., not caused by accompanying heat) effects on biologics has been widely debated due to a relative paucity of comprehensive critical details in published reports dealing with this issue. In this study, we used rigorous control over experimental conditions ... More