PARP/Apoptosis Chemiluminescent Assay Kit
PARP/Apoptosis Chemiluminescent Assay Kit Summary
• Chemiluminescent readout
• 96 well format
• Highly sensitive – detects 0.1 mU PARP ~500 cells
• Dynamic range between 0.1 to 10 mU PARP
• Requires 10-100 ng extract for detection
• Assay Time ~3 hrs
Why Use the PARP/Apoptosis Chemiluminescent Assay Kit?
This ELISA based assay detects poly (ADP-ribose) deposited by PARP-1 onto immobilized histones in a 96-well format. An anti-PAR monoclonal detecting antibody followed by addition of a goat anti-rabbit IgG-HRP secondary and a chemiluminescent HRP substrate yields relative light units (RLU) that correlates with PARP-1 activity. During apoptosis PARP-1 is cleaved with a resulting drop in activity. Etoposide is included as a control apoptosis inducer.
- Measure PARP-1 activity in cell extracts before and after apoptosis.
- For the screening of candidate PARP-1 inhibitors and determination of IC50 values.
• 10X Activated DNA
• PARP-HSA, 10 mUnits/µl
• 20 mM NAD
• Anti-PAR monoclonal Antibody
• Goat anti-mouse IgG-HRP
• 10 mM Etoposide
• 20X I-PAR Assay Buffer
• PARP PeroxyGlow A
• PARP PeroxyGlow™ B
• 5X Antibody Diluent
• Histone-Coated White Strip Well Plate, I-PAR
For research use only. Not for diagnositic use.
Citation for PARP/Apoptosis Chemiluminescent Assay Kit
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
1 Citation: Showing 1 - 1
MUC1-C INTEGRATES CHROMATIN REMODELING AND PARP1 ACTIVITY IN THE DNA DAMAGE RESPONSE OF TRIPLE-NEGATIVE BREAST CANCER CELLS
Authors: M Yamamoto, C Jin, T Hata, Y Yasumizu, Y Zhang, D Hong, T Maeda, M Miyo, M Hiraki, Y Suzuki, K Hinohara, H Rajabi, D Kufe
Cancer Res., 2019;0(0):. 2019
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