刃天青，钠盐
刃天青，钠盐
引用和文献 (305)
Invitrogen™

刃天青，钠盐

非荧光刃天青可用作荧光氧化还原指示剂，在多种细胞（包括细菌、酵母和真核生物）中，通过流式细胞仪、荧光显微镜和高通量筛选进行检测。红色荧光产品 - 刃天青最大吸收/发射波长为 ∼575/585 nm了解更多信息
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货号数量
R1220410 mg
货号 R12204
价格（CNY)
2,332.00
Each
添加至购物车
数量:
10 mg
价格（CNY)
2,332.00
Each
添加至购物车
非荧光刃天青可用作荧光氧化还原指示剂，在多种细胞（包括细菌、酵母和真核生物）中，通过流式细胞仪、荧光显微镜和高通量筛选进行检测。红色荧光产品 - 刃天青最大吸收/发射波长为 ∼575/585 nm。
仅供科研使用。不可用于诊断程序。
规格
描述刃天青，钠盐
检测方法荧光
染料类型盐
形式实心
产品规格管装
数量10 mg
运输条件室温。
颜色红色
发射585 nm
Excitation Wavelength Range575 nm
适用于（应用）活力测定试剂盒
适用于（设备）微孔板读数仪
产品线Invitrogen
产品类型刃天青
Unit SizeEach
内容与储存
室温避光储存。

常见问题解答 (FAQ)

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。

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 (305)

引用和文献
Abstract
Rapid screening of natural products for antimycobacterial activity by using luciferase-expressing strains of Mycobacterium bovis BCG and Mycobacterium intracellulare.
Authors:Shawar RM,Humble DJ,Van Dalfsen JM,Stover CK,Hickey MJ,Steele S,Mitscher LA,Baker W
Journal:Antimicrobial agents and chemotherapy
PubMed ID:9055994
The object of this study was to investigate the ability of a rapid luciferase assay to detect antimycobacterial activity in plant extracts. Recombinant strains of Mycobacterium bovis BCG (rBCG) and Mycobacterium intracellulare expressing firefly luciferase were used as the test organisms. Assays were conducted in a 96-well minitube format under ... More
Inhibition of growth and sensitization to cisplatin-mediated killing of ovarian cancer cells by polyphenolic chemopreventive agents.
Authors:Chan MM, Fong D, Soprano KJ, Holmes WF, Heverling H
Journal:J Cell Physiol
PubMed ID:12447990
'The polyphenolic compounds curcumin and quercetin increased sensitivity of ovarian cancer cells (CAOV3 and SKOV3) to cisplatin. The effect was obtained when the compounds were added simultaneously with cisplatin, as well as when they were added 24 h before. High serum levels of certain cytokines, for example interleukin-6 (IL-6), have ... More
Mechanism of target cell recognition by natural killer cells: characterization of a novel triggering molecule restricted to CD3- large granular lymphocytes.
Authors:Frey JL, Bino T, Kantor RR, Segal DM, Giardina SL, Roder J, Anderson S, Ortaldo JR
Journal:J Exp Med
PubMed ID:1720812
'In an attempt to identify a molecule in target recognition by CD3- large granular lymphocytes (LGL), we have generated a rabbit antiidiotypic (anti-ID) serum against a monoclonal antibody (mAb 36) that reacted with the cell membrane of K562. Flow cytometry analysis demonstrated that the anti-ID serum bound selectively to CD3- ... More
Functional in vivo MHC class II loading by endogenously synthesized glycoprotein during viral infection.
Authors:Oxenius A, Bachmann MF, Mathis D, Benoist C, Zinkernagel RM, Hengartner H
Journal:J Immunol
PubMed ID:9190921
'MHC class II presentation of antigenic peptides derived from soluble proteins is usually preceded by antigenic uptake via (nonreceptor-mediated) endocytosis by professional APCs, followed by processing in endosomal compartments. Although in vitro alternative pathways for MHC class II loading have been described for certain intracellularly synthesized proteins, the importance of ... More
Cell proliferation enhances entry of Listeria monocytogenes into intestinal epithelial cells by two proliferation-dependent entry pathways.
Authors:Velge P, Bottreau E, Van-Langendonck N, Kaeffer B
Journal:J Med Microbiol
PubMed ID:9511817
'Bacterial entry into intestinal host cells is the result of a fairly sophisticated manipulation of host cell machinery by the pathogens. To study further the potential cell target of Listeria spp., the in-vitro entry of L. monocytogenes strains into intestinal cells was examined in relation to the metabolism, proliferation and ... More
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