Home » Cell Apoptosis Assay » Andy Fluor™ 488 Annexin V and PI Apoptosis Kit

 

Andy Fluor™ 488 Annexin V and PI Apoptosis Kit

Introduction

Our Andy Fluor™ 488 Annexin V and PI Apoptosis Kit is used to detect the externalization of phosphatidylserine in apoptotic cells. This kit provides a sensitive two-color assay that employs our green-fluorescent Andy Fluor™ 488 annexin V and a ready-to-use solution of the red-fluorescent propidium iodide nucleic acid stain.  Propidium iodide is impermeant to live cells and apoptotic cells but stains necrotic cells with red fluorescence, binding tightly to the nucleic acids  in the cell. After staining a cell population with Andy Fluor™ 488 annexin V and propidium iodide in the provided binding buffer, apoptotic cells show green fluorescence, dead cells show red and green fluorescence, and live cells show little or no fluorescence. These populations can easily be distinguished using a flow cytometer with the 488 nm spectral line of an argon-ion laser for excitation.

Specifications

Platform: Fluorescence Cytometer
Detection Method: Fluorescent
Ex/Em: PI: 535/617 nm; Andy Fluor™ 488: 495/520 nm
Storage Conditions: 4 ℃, protect from light
Shipping Condition: Ice pack

Applications

Cell apoptosis analysis.

 

 

Figure 1. Jurkat cells treated with 10 μM camptothecin for four hours (right panel) or untreated (as control, left panel). Cells were then treated with the reagents in the kit, followed by flow cytometric analysis.

To Order

Buy Cat.No. Product Name Ex/Em Unit Price
A027-20T Andy Fluor™ 488 Annexin V and PI Apoptosis Kit 495/520 20 assays 500
A027-100T Andy Fluor™ 488 Annexin V and PI Apoptosis Kit 495/520 100 assays 1800

Documents

 

Protocol (PDF): A027
MSDS (PDF):  A027
COA (PDF):  A027


​Cited Reference:

Erianin, a promising agent in the treatment of glioblastoma multiforme triggers apoptosis in U373 and A172 glioblastoma cells
Sema Serter Kocoglu, Mücahit Seçme, Levent Elmas
Arch Biol Sci. 2022;74(3):227-234; https://doi.org/10.2298/ABS220219021S


Erianin, a promising agent in the treatment of glioblastoma multiforme triggers apoptosis in U373 and A172 glioblastoma cells
Serter Koçolu S, Seçme M, Elmas L.
Arch Biol Sci 2022, 74(3):227-34. https://doi.org/10.2298/ABS220219021S


Copper Nanoparticles Induce Oxidative Stress via the Heme Oxygenase 1 Signaling Pathway in vitro Studies
Zou L, Cheng G, Xu C, Liu H, Wang Y, Li N, Fan X, Zhu C, Xia W
Int J Nanomedicine. 2021, 16:1565-1573. doi: 10.2147/IJN.S292319


Activation of Aquaporin 5 by carcinogenic Helicobacter pylori infection promotes epithelial-mesenchymal transition via the MEK/ERK pathway
Li, N., Xu, X., Yang, H., Wang, H., Ouyang, Y., Zhou, Y., … Hong, J.
Helicobacter. 2021,00:e12842. https://doi.org/10.1111/hel.12842


Fresh and cultured mouse islets differ in their response to nutrient stimulation
Morsi M, Schulze T, Früh E, Brüning D, Panten U, Rustenbeck I.
Endocr Connect. 2020, 9(8):769-782. doi: 10.1530/EC-20-0289


Naringin  induces  endoplasmic  reticulum  stress-mediated  apoptosis,  inhibits  catenin  pathway  and  arrests  cell  cycle  in  cervical  cancer  cells
Ruyin Lin, Xinxin Hu, Shaorong Chen, Qiyang Shi and Huiqing Chen
Acta Biochimica Polonica, 2020, 67, 181-188. https://doi.org/10.18388/abp.2020_5182


Pharmacological inhibition of thioredoxin reductase increases insulin secretion and diminishes beta cell viability
Brüning, D., Hatlapatka, K., Lier-Glaubitz, V. et al.
Naunyn-Schmiedeberg's Arch Pharmacol 394, 1133–1142 (2021). https://doi.org/10.1007/s00210-020-02046-2


MicroRNA function can be reversed by altering target gene expression levels
Alexander A. Svoronos, Stuart G. Campbell, Donald M. Engelman
iScience, 2021, 24, 10, 103208, https://doi.org/10.1016/j.isci.2021.103208


Monensinin Glioblastoma Multiformede Kaspaz-10 Aracılı Apoptoz Üzerine Etkileri
Sema SERTER KOÇOLU, Mücahit SEÇME
Uluda Üniversitesi Tıp Fakültesi Dergisi, 47 (3) 393-397, 2021. DOI: https://doi.org/10.32708/uutfd.999511


[11]-Chaetoglobosins with Cytotoxic Activities from Pseudeurotium Bakeri
Ruan, Hanli and Duan, Fangfang and Gao, Ying and Peng, Xiaogang and Meng, Xianggao and Chang, Jinling and Gan, Yutian and Ouyang, Qianxi
SSRN: http://dx.doi.org/10.2139/ssrn.4102564