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主营:分子类,蛋白类,抗体类,生化类试剂
℡ 4000-520-616
℡ 4000-520-616
Cell Technology/JC1/100/JC100
产品编号:JC100
市  场 价:¥5500.00
场      地:美国(厂家直采)
产品分类: 分子类>分子诊断>
联系QQ:1570468124
电话号码:4000-520-616
邮      箱: info@ebiomall.com
美  元  价:$275.00
品      牌: Cell Technology
公      司:CellTechnology
公司分类:
Cell Technology/JC1/100/JC100
商品介绍
  • Description
  • Additional Information
  • Readable Documents
  • Assay Principle
  • Reviews

Key Benefits

  • Cell permeability allow direct measurement of apoptosis and mitochondrial potential in live cells.
  • Applications – Cells can be analyzed by Flow Cytometry, Fluorescent plate reader or Fluorescent microscopy.
  • Incubate for 15 minutes, wash and measure.
  • Add this reagent directly to live cells in your media of choice.

Additional information

Kit Size

100

Detection of the mitochondrial permeability transition event provides an early indication of the initiation of cellular apoptosis. This process is typically defined as a collapse in the electrochemical gradient across the mitochondrial membrane, as measured by the change in the membrane potential (YD). Loss of mitochondrial (YD) is indicative of apoptosis and can be detected by a unique fluorescent cationic dye, 5,5′,6,6′-tetrachloro-1,1′,3,3′-tetraethyl- benzamidazolocarbocyanin iodide, commonly known as JC-1. This dye has been incorporated into the user-friendly kit for the simple and reproducible detection of the membrane potential (YD) event in apoptotic cells. The kit has been formatted for use on Flow cytometers, Fluorescent plate readers and Fluorescent Microscopes

mitocondril_membran_a_b_1Fig (A). Jurkat cells were cultured with DMSO for 2 hours. Cells were then stained with JC-1 Mitochondrial Membrane Potential Detection Kit for 15 minutes and analyzed by flow cytometry.

mitocondril_membran_a_b_2_1Fig (B). urkat cells were cultured with staurosporine for 2 hours. Cell were then stained with JC-1 Mitochondrial Membrane Potential Detection Kit for 15 minutes and analyzed by flow cytometry.

Document Title
JC1Protocol
JC1 Datasheet
msds.JC100
TitleFileLinkAuthor(s)JournalYear; Edition:Pages
http://www.jem.org/cgi/content/full/199/4/547http://www.jem.org/cgi/content/full/199/4/547
Defects in Cell Growth Regulation by C 18:0-Ceramide and Longevity Assurance Gene 1 (LAG1) in Human Head and Neck Squamous Cell Carcinomas (HNSCC)Serap Koybasi, Can E. Senkal, Kamala Sundararaj, et alJBC Papers in PressPublished on August 17, 2004 as Manuscript M406920200
Effects of a series of organosulfur compounds on mitotic arrest and induction of apoptosis in colon cancer cellshttp://mct.aacrjournals.org/cgi/content/full/4/9/1388Danhua Xiao, John T. Pinto, Gregg G. Gundersen & Bernard WeinsteinMol Cancer Ther2005;4:1388-1398
Adrenergic receptor-stimulated apoptosis in adult cardiac myocytes involves MMP-2-mediated disruption of β1 integrin signaling and mitochondrial pathwayhttp://ajpcell.physiology.org/cgi/content/abstract/290/1/C254Bindu Menon,Mahipal Singh, Robert Ross, Jennifer N. Johnson and Krishna SinghAm J Physiol Cell Physiol290: C254-C261, 2006. First published September 7, 2005
SGLT-1-mediated glucose uptake protects intestinal epithelial cells against LPS-induced apoptosis and barrier defects: a novel cellular rescue mechanism?http://www.fasebj.org/cgi/content/abstract/19/13/1822Linda C. H. Yu Andrew N. Flynn, Jerrold R. Turner and Andre G. BuretThe FASEB Journal2005;19:1822-1835
Ceramide induces mitochondrial abnormalities in insulin-secreting INS-1 cells: Potential mechanisms underlying ceramide-mediated metabolic dysfunction of the β cellhttp://www.springerlink.com/content/t3g0p313518r2747/R. Veluthakal, R. Palanivel Y. Zhao, P. McDonald, S. Gruber and A. KowluruApoptosis JournalVol 10/No 4, Aug 2005
Opposing effects of bovine papillomavirus type 1 E6 and E7 genes on Fas-mediated apoptosishttp://www.nature.com/onc/journal/v24/n24/abs/1208542a.htmlYun Liu, Zhiguo Liu, Hua Gao, You Zhou, Elliot J Androphy and Jason J ChenOncogene(March 2005) 24, 3942–3953
Resveratrol-caused apoptosis of human prostate carcinoma LNCaP cells is mediated via modulation of phosphatidylinositol 3"-kinase/Akt pathway and Bcl-2 family proteinshttp://mct.aacrjournals.org/cgi/content/abstract/5/5/1335Moammir H. Aziz,Minakshi Nihal, Vivian X. Fu, David F.Jarrard and N AhmadMol Cancer Ther2006;5:1335-1341
Reference
Desagher, S., Osen-Sand, A., Nichols, A., Eskes, R., Montessuit, S., Lauper, S., Maundrell, K., Antonsson, B., and Martinou, J.C. Bid-induced conformational change of Bax is responsible for mitochondrial cytochrome c release during apoptosis. J. Cell Biol. 144 (5): 891-901 (1999).
Narita, M., Shimizu, S., Ito, T., Chittenden, T., Lutz, R. J., Matsuda, H., and Tsujimoto, Y. Bax interacts with the permeability transition pore to induce permeability transition and cytochrome c release in isolated mitochondria. Proc. Natl. Acad. Sci. USA 95: 14681-14686 (1998).
Basanez, G., Nechushtan, A., Drozhinin, O., Chanturiya, A., Choe, E., Tutt, S., Wood, K. A., Hsu, Y. T., Zimmerberg, J., and Youle, R. J. Bax , but not Bcl-XL decreases the lifetime of planar phospholipid bilayer membranes at subnanomolar concentrations. Proc. Natl. Acad. Sci. USA 96: 5492-5497 (1999).
Luo, X., Budihardio, I., Zou, H., Slaughter, C., and Wang, X. Bid, a Bcl-2 interacting protein, mediates cytochrome c release from mitochondria in response to activation of cell surface death receptors. Cell 94: 481-490 (1998).
Smiley, S. T., Reers, M., Mottola-Hartshorn, C., Lin, M., Chen, A., Smith, T. W., Steele, G.D., and Chen, L. B. Intracellular heterogeneity in mitochondrial membrane potentials revealed by a J-aggregate forming lipophilic cation JC-1. Proc. Natl. Acad. Sci. USA 88: 3671-3675 (1991).
Cossarizza, A., Baccarani-Contri, M., Kalashnikova, G., and Franceschi, C. A new method for the cytofluorimetric analysis of mitochondrial membrane potential using the J-aggregate forming lipophilic cation 5,5’,6,6’-tetrachloro-1,1’,3,3’-tetraethylbenzimidazolylcarbocyanine iodide (JC-1). Biochem. Biophys. Res. Commun. 197 (1): 40-45 (1993).
Reers, M., Smith, T. W., and Chen, L. B. J-aggregate formation of a carbocyanine as a quantitative fluorescent indicator of membrane potential. Biochemistry 30: 4480-4486 (1991).
White, R. J., and Reynolds, I. J. Mitochondrial depolarization in glutamatestimulated neurons: an early signal specific to excitotoxin exposure. Journal of Neuroscience 16: 5688-5697 (1996).
Part#ReagentTemperature
Part# 4001Lyophilized JC-1 DyeStore at 2-8C
Part# 300210X Assay BufferStore at 2-8C

Please select an ACF field to output

品牌介绍

Cell Signaling Technology (CST) 是一家由科学家创立的私营家族公司,致力于提供全球最高品质的创新研究和诊断产品,加速生物学认知以及实现个体化医疗。CST坚持自主生产和严格验证,其高质量的产品和专业的研发精神已被全球客户认可,被公认/票选为细胞信号研究的金标准、最佳抗体*、研究者的选择*、PTM(蛋白翻译后修饰)年度抗体公司*、十年抗体品牌*等(*来自CiteAb、LISA数据报告)。

CST提供最高品质的特色信号蛋白及磷酸化、甲基化、乙酰化、泛素化、SUMO化等翻译后修饰抗体,蛋白翻译后修饰筛选试剂盒及服务,还有偶联抗体,二抗,ChIP试剂盒,细胞因子,ELISA试剂盒,细胞检测试剂盒,蛋白实验配套试剂等,为您提供蛋白相关实验的一站式解决方案。


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