钙红素 AM 货号22011-AAT Bioquest荧光染料

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钙红素 AM

钙红素 AM

钙红素 AM    货号22011 货号 22011 存储条件 在零下15度以下保存, 避免光照
规格 1 mg 价格 2544
Ex (nm) 643 Em (nm) 663
分子量 ~1000 溶剂 DMSO
产品详细介绍

简要概述

产品基本信息

货号:22011

产品名称:钙红素 AM

规格:1mg

储存条件:-15℃避光防潮

保质期:12个月

 

产品物理化学光谱特性

分子量:~1000

溶剂:DMSO

激发波长(nm):643

发射波长(nm):663

 

适用仪器


流式细胞仪  
激发: 633/640nm激光
发射: 660/20nm滤波片
通道: APC通道
荧光显微镜  
激发: Cy5滤波片
发射: Cy5滤波片
推荐孔板: 黑色透明

 

产品介绍

钙黄绿素AM是最流行的荧光探针之一,用于标记和监测活细胞的细胞功能。但是,钙黄绿素AM的单色使得无法在多色应用中使用这种有价值的试剂。例如,与GFP相同的颜色,不可能将Calcein AM与GFP转染的细胞结合使用。为了解决钙黄绿素AM的颜色限制,我们开发了Calcein Orange,Calcein Red和Calcein Deep Red。这些新的钙黄绿素AM酯与钙黄绿素AM结合使用可对活细胞进行多色标记和功能分析。非荧光钙红绿素 AM酯很容易进入活细胞并水解,产生强荧光的钙红绿素 (Cat#:21902)染料。钙红绿素染料可以用通用的Cy5滤波器组进行检测。金畔生物是AAT Bioquest的中国代理商,为您提供最优质的钙红素 AM。 

点击查看光谱

 

图示

钙红素 AM    货号22011

图1.用钙黄绿素Deep Red AM酯(Cat#22011)染色的Jurkat细胞的流式细胞术分析。将Jurkat细胞用HH缓冲液洗涤一次,并在37°C下用含0.02%PF-127(Cat#20053)和1mM PBC(Cat#20061)的2 uM Calcein Deep Red AM酯(Cat#22011)染色30分钟。然后用HH缓冲液洗涤细胞,并重悬于HH缓冲液中。使用蓝色激光APC发射通道,用NovoCyte 3000流式细胞仪测量活细胞(红色)和死细胞(在55°C水浴中处理30分钟,绿色)的荧光强度。 

 

参考文献

A ratiometric fluorescent assay for the detection and bioimaging of alkaline phosphatase based on near infrared Ag2S quantum dots and calcein
Authors: Cai, M., Ding, C., Wang, F., Ye, M., Zhang, C., Xian, Y.
Journal: Biosens Bioelectron (2019): 148-153

Calcein release assay as a method for monitoring serum complement activity during monoclonal antibody therapy in patients with B-cell malignancies
Authors: Stasilojc, G., Felberg, A., Urban, A., Kowalska, D., Ma, S., Blom, A. M., Lundin, J., Osterborg, A., Okroj, M.
Journal: J Immunol Methods (2019): 112675

Contribution of headgroup and chain length of glycerophospholipids to thermal stability and permeability of liposomes loaded with calcein
Authors: Prislan, I., Lokar, M., Zirdum, M., Valant, J., Poklar Ulrih, N.
Journal: Chem Phys Lipids (2019): 104807

Doxorubicin as a fluorescent reporter identifies novel MRP1 (ABCC1) inhibitors missed by calcein-based high content screening of anticancer agents
Authors: Sampson, A., Peterson, B. G., Tan, K. W., Iram, S. H.
Journal: Biomed Pharmacother (2019): 109289

Factors Affecting the Acoustic In Vitro Release of Calcein from PEGylated Liposomes
Authors: Ahmed, S. E., Moussa, H. G., Martins, A. M., Abbas, Y., Al-Sayah, M. H., Husseini, G. A.
Journal: J Nanosci Nanotechnol (2019): 6899-6906

Ratio fluorometric determination of ATP base on the reversion of fluorescence of calcein quenched by Eu(III) ion using carbon dots as reference
Authors: Zhang, C., Zhang, H., Yu, Y., Wu, S., Chen, F.
Journal: Talanta (2019): 451-456

Calcein Release from Cells In Vitro via Reversible and Irreversible Electroporation
Authors: Rajeckaite, V., Jakstys, B., Rafanavicius, A., Maciulevicius, M., Jakutaviciute, M., Satkauskas, S.
Journal: J Membr Biol (2018): 119-130

Calcein leakage as a robust assay for cytochrome c/H2O2-mediated liposome permeabilization
Authors: Firsov, A. M., Kotova, E. A., Antonenko, Y. N.
Journal: Anal Biochem (2018): 19-23

Light scattering corrections to linear dichroism spectroscopy for liposomes in shear flow using calcein fluorescence and modified Rayleigh-Gans-Debye-Mie scattering
Authors: Dorrington, G., Chmel, N. P., Norton, S. R., Wemyss, A. M., Lloyd, K., Praveen Amarasinghe, D., Rodger, A.
Journal: Biophys Rev (2018): 1385-1399

A Label-Free Fluorescent Array Sensor Utilizing Liposome Encapsulating Calcein for Discriminating Target Proteins by Principal Component Analysis
Authors: Imamura, R., Murata, N., Shimanouchi, T., Yamashita, K., Fukuzawa, M., Noda, M.
Journal: Sensors (Basel) (2017): se name=”22011.enl” path=”C:UsersaatbiDropboxCatalogs & Website Working FilesProduct References22011.enl”>22011.enlEndNote121217Imamura, R.Murata, N.Shimanouchi, T.Yamashita, K.Fukuzawa, M.Noda, M.Graduate School of Science and Technology, Kyoto

说明书
钙红素 AM.pdf