LIVE/DEAD™ 细胞活力检测试剂盒,C12 刃天青/SYTOX™ 绿色
LIVE/DEAD&trade; 细胞活力检测试剂盒,C<sub>12</sub> 刃天青/SYTOX&trade; 绿色
Invitrogen™

LIVE/DEAD™ 细胞活力检测试剂盒,C12 刃天青/SYTOX™ 绿色

The LIVE/DEAD Cell Vitality Assay Kit provides a simple, two-color fluorescence assay that distinguishes metabolically active cells from injured cells了解更多信息
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货号数量
L349511000 次检测
货号 L34951
价格(CNY)
4,325.00
飞享价
Ends: 31-Dec-2025
5,746.00
共减 1,421.00 (25%)
Each
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数量:
1000 次检测
价格(CNY)
4,325.00
飞享价
Ends: 31-Dec-2025
5,746.00
共减 1,421.00 (25%)
Each
添加至购物车
The LIVE/DEAD Cell Vitality Assay Kit provides a simple, two-color fluorescence assay that distinguishes metabolically active cells from injured cells and dead cells. The assay is based on the reduction of C12-resazurin to red-fluorescent C12-resorufin in metabolically active cells and on the uptake of the cell-impermeant, green-fluorescent nucleic acid stain, SYTOX Green dye, in cells with compromised plasma membranes (usually late apoptotic and necrotic cells). In this assay, dead cells emit mostly green fluorescence and healthy, metabolically active cells emit mostly red fluorescence; injured cells exhibit reduced red and green fluorescence.

View a selection guide for all Cell Viability Assays for Flow Cytometry.
仅供科研使用。不可用于诊断程序。
规格
细胞渗透性不透过、透过
细胞类型哺乳动物细胞、真核细胞
描述LIVE/DEAD™ 细胞活性测定试剂盒,C12 刃天青/SYTOX™ 绿色
检测方法荧光
染料类型其他标记或染料
产品规格
数量1000 次检测
运输条件室温
溶解度DMSO(二甲亚砜)
颜色绿色、红色
发射C12 刃天青:563/587 nm
SYTOX™ Green:504/523 nm
Excitation Wavelength Range504/563 nm
适用于(应用)活力测定试剂盒
适用于(设备)荧光显微镜, 流式细胞仪, 微孔板读数仪
产品线LIVE/DEAD,SYTOX
产品类型细胞活力测定试剂盒
Unit SizeEach
内容与储存
包含5小瓶 C12 刃天青(每小瓶40 μg)、1小瓶 SYTOX™ Green(100 μL,10 μM 溶液,溶于 DMSO 中)、1小瓶 DMSO (1.5 mL) 和 10X 磷酸盐缓冲液 (100 mL)。

在冷柜(-5°C 至 -30°C)中避光储存。

常见问题解答 (FAQ)

这些染料如何与DNA结合?

SYTO核酸染料的结合方式尚不清楚。但是,SYTO以及相关的核酸染料具有以下结合特性:

1.它们与一些溶剂结合(通过对盐、二价阳离子的敏感性,特别是SDS),因此,它们可能结合到DNA沟槽处。
2.所有SYTO染料都表现出一些碱基选择性,因此,它们可能结合到DNA小沟处。
3.通过乙醇沉淀可从核酸中去除SYTO染料;溴化乙锭和其他嵌入剂不具有此特性。同样,丁醇和氯仿提取不能从核酸中去除SYTO染料,但能够去除溴化乙锭。
4.SYTO 结合不受非离子去垢剂的影响。
5.SYTO染料不会被BrdU淬灭,因此,SYTO染料与核酸的结合方式不同于Hoechst 33342和DAPI(4',6-二脒基-2-苯基吲哚)。

SYBR Green I对移码指示菌几乎没有致突变性,证明其不大可能是强嵌入剂。

alamarBlue试剂和PrestoBlue试剂与刃天青和C12-刃天青有什么不同?

alamarBlue试剂和PrestoBlue试剂含有的刃天青包含在一种专有的稳定配方中,能够提供了一种便捷的“混合、接种和读数”实验方案。PrestoBlue试剂是alamarBlue试剂的改进配方允许更快速的染色(典型的10分钟相比于1-4小时获得相似的信号和灵敏度)。C12-刃天青是刃天青的衍生物,其拥有良好的细胞滞留性,因此适用于伴有活性指示剂和其他生物标记的流式细胞分析仪多重检测分析。

我如何为LIVE/DEAD细胞活力实验准备死细胞对照?

有两种简单的方法。一种是通过60°C放置20分钟热灭活细胞。第二种是将细胞放入70%乙醇。乙醇固定的细胞可以在冰箱中无限期储存直到使用,可达好几年。

1.离心细胞、使细胞沉淀并去除上清
2.固定细胞:在15mL含有细胞团的试管中加入10 mL70%冰乙醇,先开始逐滴加入后震荡,混合均匀。
3.在冰箱中储存直到使用。
4.快使用时,水洗两次且在选择的缓冲液中重悬。

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.

引用和文献 (4)

引用和文献
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