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7-AAD/CFSE Cell-Mediated Cytotoxicity Assay Kit
Cellular Assay Kits
Assay Kit

7-AAD/CFSE Cell-Mediated Cytotoxicity Assay Kit #72782

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Flow Cytometry Image 1: 7-AAD/CFSE Cell-Mediated Cytotoxicity Assay Kit
Flow cytometric analysis of target K562 cells (top row) or SUP-B15 cells (bottom row) labeled with CFSE, incubated with (right column) or without (left column) effector NK-92 cells at a 12:1 effector:target cell ratio for 4 h, and stained with 7-AAD for 15 min. Cells that stain positive for both 7-AAD and CFSE represent dying target cells and are located in Q2 of the dot plot.
To Purchase # 72782S
Product # Size Price
1 Kit  (100 assays) $ 249

Product Includes Quantity (with Count) Solution Color
7-AAD Viability Dye 2 x 50 µl
CFSE Stock Solution 1 x 100 µl
Cell-Based Assay Buffer Tablet 1 x 4 ea



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Protocol Id: 1964

Product Description

The 7-AAD/CFSE Cell-Mediated Cytotoxicity Assay Kit employs CFSE (carboxyfluorescein succinimidyl ester) to label target cells within the mixed cell population and 7-AAD (7-aminoactinomycin D) to label dead cells. This kit provides an improvement over the traditional chromium-51 (51Cr) release assay to assess cell-mediated cytotoxicity. CFSE labeling is more sensitive, does not employ radioisotopes, and cytolysis can be assessed at the single-cell level using flow cytometry.
CAS 7240-37-1, 67-68-5, 150347-59-4


Cytolytic assays are routinely used to interrogate immune effector cell function. In order to interrogate immune effector cell cytolytic activity in a heterogeneous cell population of effector and target cells, it is imperative to be able to discriminate between effector and target cell populations with distinct phenotypes. As such, this kit is designed to label live target cells with the membrane permeable fluorescent dye CFSE prior to coculture with unlabelled effector cells, thus permitting a clear separation between live effector and target cells. After incubation of live effector and target cells, the DNA intercalating dye 7-AAD is added to label dying target cells with compromised plasma membranes. By using dyes with distinct spectral properties, a clear separation between four cell populations can be obtained using flow cytometry: live target cells, dead target cells, live effector cells, and dead effector cells (1).
  1. Kim, G.G. et al. (2007) 325, 51-66.

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