Human Cleaved-PARP (D214/G215) and PARP ELISA

RayBio® Human Cleaved PARP (D214/G215) and PARP ELISA Kit. This ELISA is for measuring cleaved PARP (Asp-214/Gly-215) as well as PARP in human cell lysates.


Antigen Information

Accession Number:
  • P09874
Gene ID:
  • 142
Gene Symbols:
  • PARP1
  • PPOL
Protein Name & Synonyms:
Poly [ADP-ribose] polymerase 1 (PARP-1) (EC (ADP-ribosyltransferase diphtheria toxin-like 1) (ARTD1) (NAD(+) ADP-ribosyltransferase 1) (ADPRT 1) (Poly[ADP-ribose] synthase 1)

Assay Format

  • Apoptosis
  • DNA Damage
The antibody pair provided in this kit recognizes human PARP cleaved at sites aspartic acid-214 and glycine-215.
Number of Targets Detected:
Species Detected:
  • Human
Compatible Sample Types:
  • Cell Lysates
  • Tissue Lysates
Design Principle:
  • Sandwich-based
Method of Detection:
Solid Support:
96-well Microplate

Product Specifications

1, 2, or 5 x 96-Well Strip Microplate Kit


RayBio® Cleaved-PARP (Asp214/Gly215) and PARP ELISA kit is a very rapid, convenient and sensitive assay kit that can monitor the activation or function of important biological pathways in human cell lysates. Bydetermining cleaved PARP protein in your experimental model system, youcan verify pathway activation in your cell lysates. You can simultaneouslymeasure numerous different cell lysates without spending excess time andeffort in performing a Western Blotting analysis.

This Sandwich ELISA kit is an in vitro enzyme-linkedimmunosorbent assay for the measurement of human Cleaved-PARP andPARP. An anti-PARP antibody has been coated onto a 96-well plate.Samples are pipetted into the wells and PARP present in a sample is boundto the wells by the immobilized antibody. The wells are washed and rabbitanti-Cleaved-PARP (Asp214/Gly215) antibody is used to detect CleavedPARP or rabbit anti-PARP antibody is used to detect PARP. After washingaway unbound antibody, HRP-conjugated anti-rabbit IgG is pipetted to thewells. The wells are again washed, a TMB substrate solution is added to thewells and color develops in proportion to the amount of Cleaved PARP(Asp214/Gly215) or PARP bound. The Stop Solution changes the color fromblue to yellow, and the intensity of the color is measured at 450 nm.

Product Features

  • Simultaneously measure cleaved protein and pan protein in one experiment (for normalization purpose)
  • Screen numerous different cell lysates without performing a Western Blot analysis
  • Minimal hands-on time, convenient, and non-radioactive material

Application Notes

Kit Components
  • Pre-Coated 96-well Strip Microplate
  • Wash Buffer
  • Anti-cleaved PARP Antibody
  • Anti-PARP Antibody
  • HRP-Conjugated Secondary Antibody
  • Assay Diluent
  • TMB One-Step Substrate
  • Stop Solution
  • Lysis Buffer
  • Positive Control Sample
Other Materials Required
  • Distilled or deionized water
  • 100 ml and 1 liter graduated cylinders
  • Tubes to prepare sample dilutions
  • Protease and Phosphatase inhibitors
  • Precision pipettes to deliver 2 µl to 1 ml volumes
  • Adjustable 1-25 ml pipettes for reagent preparation
  • Benchtop rocker or shaker
  • Microplate reader capable of measuring absorbance at 450 nm
Protocol Outline
  1. Prepare all reagents and samples as instructed in the manual.
  2. Add 100 µl of sample or positive control to each well.
  3. Incubate 2.5 h at RT or O/N at 4 °C.
  4. Add 100 µl of prepared primary antibody to each well.
  5. Incubate 1 h at RT.
  6. Add 100 µl of prepared 1X HRP-Streptavidin to each well.
  7. Incubate 1 h at RT.
  8. Add 100 µl of TMB One-Step Substrate Reagent to each well.
  9. Incubate 30 min at RT.
  10. Add 50 µl of Stop Solution to each well.
  11. Read at 450 nm immediately.

Typical Data

Positive Control
HeLa cells were treated with STS (Staurosporine). Solubilize cells at 4 x 107 cells/ml in Cell Lysate Buffer. Serial dilutions of lysates were analyzed in this ELISA. Please see step 3 of Part VI Reagent Preparation for detail.
STS Stimulation of HeLa Cell Line
HeLa cells were treated or untreated with STS. Cell lysates were analyzed using this ELISA and Western Blot.


Upon receipt, the kit should be stored at –20°C. Please use within 6 months from the date of shipment. After initial use, Wash Buffer Concentrate (Item B), Assay Diluent (Item E), TMB One-Step Substrate Reagent (Item H), Stop Solution (Item I) and Cell Lysate Buffer (Item J) should be stored at 4°C to avoid repeated freeze-thaw cycles. Return unused wells to the pouch containing desiccant pack, reseal along entire edge, and store at –20°C. Item D, store at 2-8°C for up to one month (store at -20°C for up to 6 months, avoid repeated freeze-thaw cycles). Reconstituted Positive Control (Item K) should be stored at -70°C.

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This product is furnished for LABORATORY RESEARCH USE ONLY.
Not for diagnostic or therapeutic use.

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