PARP2 Homogeneous Assay Kit (Discontinued)

Catalog #
80702
$1,470 *
Catalog number 80702, PARP2 Homogeneous Assay Kit (Discontinued), has been discontinued. Please find our suggested alternative here.
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Description

The PARP2 Homogeneous Assay Kit is designed to measure PARP2 activity for screening and profiling applications. PARP2 is known to catalyze the NAD-dependent addition of poly(ADP-ribose) to histones. The key to the PARP2 Homogeneous Assay Kit is a highly specific antibody that recognizes PARylated substrate. With this kit, only three simple steps are required for PARP2 reactions. First, a sample containing PARP2 enzyme is incubated with activated DNA and biotinylated substrate for one hour. Next, acceptor beads and primary antibody are added, then donor beads, followed by reading the Alpha-counts.

Synonyms
poly (ADP-ribose) polymerase 2, poly(ADP-ribosyl)transferase 2, ADPRT, ADPRTL2
Product Info
Storage and Usage
Citations
Assay Kit Format
AlphaLISA®
Supplied As
The PARP2 Homogeneous Assay Kit comes in a convenient AlphaLISA® format, with biotinylated histone substrate, primary antibody, PARP assay buffer, and purified PARP2 for 384 enzyme reactions.
Materials Required But Not Supplied

AlphaLISA anti-mIgG acceptor beads, 5 mg/ml (Perkin Elmer #AL105C)
AlphaScreen Streptavidin-conjugated donor beads, 5 mg/ml (Perkin Elmer #6760002S)
Optiplate -384 (Perkin Elmer #6007290)
AlphaScreen microplate reader
Adjustable micropipettor and sterile tips
0.5 M DTT

Format
Catalog
Number
Components Amount Storage 
80502 PARP2 10 μg -80°C


Avoid

freeze/
thaw
cycles!
  NAD+(750 μM) 400 μl -20°C
52140K Primary antibody 11 10 μl -80°C
  Biotinylated histone substrate* 500 rxns -80°C
80602A 10x PARP assay buffer** 1 ml -20°C
52301 4x Detection buffer 1 2 ml -20°C

 

 

 

 

 

 

 

 

 

 

*Reconstitute in 500 µl H20
**Add DTT before use

UniProt #
Q9UGN5
Background
PARP2 is known to catalyze the NAD-dependent addition of poly (ADP-ribose) to histones.
References

Brown JA, Marala RB. J. Pharmacol. Toxicol. Methods 2002 47:137-41.