Cellomics HCS Reagent Kit for detection of phosphorylated (Ser1981) Ataxia telangiectasia mutated (ATM) kinase. | | | | | control | treat cells | detect phospho–ATM | analyze | conclude |
DescriptionThe Cellomics Phospho-ATM Activation Kit contains optimized reagents for the detection and quantitation of phosphorylated ATM (Ser1981) in the nuclei. The kit contains a primary monoclonal antibody that detects only the phosphorylated form of human ATM, a goat anti-mouse secondary antibody conjugated to DyLight 549 Fluorophore and various other reagents and buffers required for immunofluorescence staining for high-content screening (HCS) assays. Ataxia telangiectasia mutated kinase (ATM, 350 kDa) is involved in cell cycle check-point signaling and DNA repair. Mutation in the ATM gene leads to ataxia telangiectasia, an autosomal recessive human disease. ATM is auto phosphorylated at Ser1981 upon induction of DNA double-strand breaks (DSBs) leading to rapid check-point signaling. ATM kinase has several identified targets including H2AX, BRCA1, NBS1, Chk1, Chk2 and p53. Phospho-ATM in the nucleus of A549 cells treated with etoposide was assayed using the Cellomics Phospho-ATM Activation Kit, the Cellomics ArrayScan HCS Reader (Figure 1) and the Compartmental Analysis BioApplication Software Module. Induction of DNA damage by etoposide leads to phosphorylation of ATM. Cells labeled using this kit also can be imaged by fluorescence or confocal microscopy. | |  | Non-treated cells | Treated cells | Dose response curve | Figure 1. Staining of Phospho-ATM in A549 cells treated with vehicle (0.1% DMSO in media) (left) or with 50 µM etoposide for 3 hours (center). Cell were stained according to the kit protocol and imaged using a Cellomics ArrayScan HCS Reader. Dose response curve for etoposide-treated A549 cells (right). Etoposide concentration is plotted against the difference between nuclear and cytoplasmic intensities for phospho-ATM. Data represents mean +/-SD from three plates (eight wells per 96-well plate per dose of etoposide). EC50 = 7.5 +/-1.1 µM. |
Related Poster Presentations | Bhaskar S. Mandavilli, Suk J. Hong, Krishna M. Vattem, and Richik N. Ghosh (2008) Quantitative, Cell-Based, High-Content Screening Assays for DNA Damage-Induced Cell Cycle Checkpoints. |
Kit Contents| Component | 8403001 | 8403002 | | Phospho-ATM Primary Antibody | 12 µl | 60 µl | DyLight 549 Conjugated
Goat Anti-Mouse IgG | 30 µl | 72 µl | | Hoechst Dye | 30 µl | 30 µl | | Wash Buffer (10X Dulbecco's PBS) | 100 ml | 100 ml | Wash Buffer II (10X Dulbecco's PBS with
1% Tween®-20) | 100 ml | 100 ml | Permeabilization Buffer (10X D-PBS with 1% Triton® X-100) | 100 ml | 100 ml | | Blocking Buffer (10X) | 85 ml | 85 ml | | Thin Plate Seal Assembly | 7/pack | 7/pack |
Ordering InformationScreening size kits and components (bulk and custom) available with special pricing. Please call. To order Cellomics HCS Reagent Kits, please call 800-874-3723 in the U.S.
or contact your local distributor of Thermo Scientific Products. Choose "Order Online" in table to see pricing and order online (U.S. only). | Buy | Product # | Description | Pkg. Size | | Order Online | 8403001 | Phospho-ATM Activation Kit | 1 x 96 | | Order Online | 8403002 | Phospho-ATM Activation Kit | 5 x 96 |
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