|Product name||Live and Dead Cell Double Staining Kit|
|Applications notes||Abbkine Live and Dead Cell Double Staining Kit provides a convenient assay to evaluate the viability of cells, based on the simultaneous determination of live and dead cells with two probes that measure recognized parameters of cell health: plasma membrane integrity and intracellular esterase activity. The kit utilizes LiveDye, a cell-permeable green fluorescent dye (Ex/Em = 488/530 nm), to stain live cells and NucleiDye, a cell non-permeable red fluorescent dye (Ex/Em = 535/617), to stain dead cells.|
|Kit components||• LiveDye
• Assay Buffer (10X)
|Features & Benefits||• Suitable for mammalian cells staining.
• Useful for the rapid quantitation of cell viability using flow cytometery or fluorescent microscopy.
• LiveDye (green, Ex/Em=488/530nm), NucleiDye (red, Ex/Em= 535/617nm).
|Usage notes||NucleiDye is a potential mutagen. Use appropriate precautions when handling this reagent.|
|Storage instructions||Refer to list of materials supplied for storage conditions of individual components. Stable for at least 12 months at recommended temperature from date of shipment.|
|Shipping||Gel pack with blue ice.|
|Precautions||The product listed herein is for research use only and is not intended for use in human or clinical diagnosis. Suggested applications of our products are not recommendations to use our products in violation of any patent or as a license. We cannot be responsible for patent infringements or other violations that may occur with the use of this product.|
|Background||Cell-mediated cytotoxicity is an important phenomenon characterized by cytolysis of a compromised cell in the body by immune system. Distinguishing between live and dead cells is very important for investigation of growth control and cell death.|
Fig.1. Hela cells stained with Abbkine Live and Dead Cell Double Staining Kit. A: Live cells stain green, B: Dead cells (30min incubation in 70% ethanol) stain red.
Fig.2. Hela cells incubated with staining solution in Abbkine Live and Dead Cell Double Staining Kit for 20min.
Author：Sun Y, Chi X, Meng H, Ma M, Wang J, Feng Z, Quan Q, Liu G, Wang Y, Xie Y, Zheng Y, Peng J Publication name：Bioact Mater IF：8.724
Author：L Zhao, Y Jia, C Zhao Publication name：Acta biomaterialia IF：6.72
Author：Ding A, Quan L, Guo X, Wang H, Wen Y, Liu J, Zhang L, Zhang D, Lu P, Publication name：Sci Total Environ IF：6.551
Author：Wang F, Zhao L, Song F, Wu J, Zhou Q, Xie L, Publication name：Journal of Materials IF：5.344
Author：Chen L, Wu C, Wang H, Chen S, Ma D, Tao Y, Wang X, Luan Y, Wang T, Shi Y, Song G, Zhao Y, Dong X, Wang B Publication name：Front Oncol IF：4.848
Author：Dou L, Zhang Y Publication name：Front Oncol IF：4.848
Author：W Wang, B Zhang, L Zhao, M Li, Y Han Publication name：Nanotechnology IF：3.874
Author：Shuangshuang Wang, Jixuan Song, Yuchao Li, et al Publication name：Reactive and Functional Polymers IF：3.21
Author：W Fu, S Liu, J Jiao, Z Xie, X Huang, Y Lu, H Liu, S Hu Publication name：Materials (Basel) IF：3.057
Author：Y Cao, S Yang, D Zhao Publication name：Journal of Orthopaedic Translation IF：2.21
1.The species of antibody reactivity should be the sample species that can be matched normally after Abbkine R&D experts have passed strict scientific verification. If your sample is not within the range of reactivity, in order to improve the efficiency and results of your experiment, it is not suggested to try other species. Otherwise, it may lead to sample mismatch and affect the effect of your experiment.
2.Please aliquot the antibody received as soon as possible and store it at -20℃, avoid repeated freezing and thawing, and use it within one year.
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