PARP [Poly(ADP-ribose) Polymerase], also known as ADPRT and PPOL, is a 118-kDa enzyme that uses NAD as a substrate to catalyze the covalent transfer of ADP-ribose to a variety of nuclear protein acceptors. ADP ribosyltransferase is required for cellular repair, and PARP expression is induced by single-strand breaks in DNA. PARP is proteolytically cleaved by Caspase-3 into two fragments of 89- and 24-kDa in one of the hallmark events of apoptosis.
Universal Chemiluminescent PARP Assay - Histone Coated Wells
R&D Systems | Catalog # 4676-096-K
Key Product Details
Features
Key Benefits
- Chemiluminescent readout
- 96 strip-well format
- Sensitive – detects 10 mU PARP /well
- Assay Time ~3 hrs
Species
Product Summary for Universal Chemiluminescent PARP Assay - Histone Coated Wells
Kit Contents for Universal Chemiluminescent PARP Assay - Histone Coated Wells
- 3-Aminobenzamide
- Human PARP 1 Enzyme, HSA
- 20X PARP Buffer
- 10X PARP Cocktail
- 10X Activated DNA
- 10X Strep-Diluent
- PeroxyGlow™ A
- PeroxyGlow™ B
- Histone-Coated White Strip Well Plate
- Strep-HRP
Formulation, Preparation, and Storage
Shipping
Storage
Background: PARP
Long Name
Alternate Names
Additional PARP Products
Product Documents for Universal Chemiluminescent PARP Assay - Histone Coated Wells
Certificate of Analysis
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Citations for Universal Chemiluminescent PARP Assay - Histone Coated Wells
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FAQs for Universal Chemiluminescent PARP Assay - Histone Coated Wells
-
Q: Does this kit contain the full-length or truncated form of PARP?
A: This is the full length PARP1 containing a short ubiquitin tag on the amino terminus.
-
Q: What is the maximum DMSO concentration in samples that can interfere with the assay?
A: Maximum DMSO concentration for inhibitor vehicles has not been evaluated. It is recommended to include a DMSO only control in the assay.
-
Q: What wavelength should be used to read the chemiluminescent plate?
A: The peroxyglow substrates used in the chemiluminescent kit are in the visible light range, so the plate reader should not filter the light source or the detector. The detector measures light intensity without specificity for a particular wavelength. The results are in all the wavelengths and report the amount of detected emitted light in relative light units or RLU. We recommend using a luminometer that is used for luciferase assays.
-
Q: Does this kit contain the full-length or truncated form of PARP?
A: This is the full length PARP1 containing a short ubiquitin tag on the amino terminus.
-
Q: What is the maximum DMSO concentration in samples that can interfere with the assay?
A: Maximum DMSO concentration for inhibitor vehicles has not been evaluated. It is recommended to include a DMSO only control in the assay.
-
Q: What wavelength should be used to read the chemiluminescent plate?
A: The peroxyglow substrates used in the chemiluminescent kit are in the visible light range, so the plate reader should not filter the light source or the detector. The detector measures light intensity without specificity for a particular wavelength. The results are in all the wavelengths and report the amount of detected emitted light in relative light units or RLU. We recommend using a luminometer that is used for luciferase assays.
-
Q: Does this kit contain the full-length or truncated form of PARP?
A: This is the full length PARP1 containing a short ubiquitin tag on the amino terminus.
-
Q: What is the maximum DMSO concentration in samples that can interfere with the assay?
A: Maximum DMSO concentration for inhibitor vehicles has not been evaluated. It is recommended to include a DMSO only control in the assay.
-
Q: What wavelength should be used to read the chemiluminescent plate?
A: The peroxyglow substrates used in the chemiluminescent kit are in the visible light range, so the plate reader should not filter the light source or the detector. The detector measures light intensity without specificity for a particular wavelength. The results are in all the wavelengths and report the amount of detected emitted light in relative light units or RLU. We recommend using a luminometer that is used for luciferase assays.