PRMT1 Chemiluminescent Assay Kit

Catalog #
52004L
$790 *
Size: 96 reactions
Qty
*US Pricing only. For international pricing, please contact your local distributor.
Purchase
Description

The PRMT1 Direct Activity Chemiluminescent Assay kit is designed to measure PRMT1 activity for screening and profiling applications. The key to the PRMT1 Chemiluminescent Assay Kit is a highly specific antibody that recognizes methylated R3 residue of Histone H4. With this kit, only three simple steps are required for methyltransferase detection. First, S-adenosylmethionine is incubated with a sample containing assay buffer and methyltransferase enzyme. Next, primary antibody is added. Finally, the strip plates are treated with an HRP-labeled secondary antibody followed by addition of the HRP substrate to produce chemiluminescence that can then be measured using a chemiluminescence reader.

Need us to run inhibitor screens or profile your compounds against PRMT1? Check out our Methyltransferase Screening Services

This product has been cited 8 times.

Synonyms
PRMT1, HRMT1L2, IR1B4, HCP1, PRMT-1
Product Info
Storage and Usage
Citations8
Assay Kit Format
Chemiluminescent
Supplied As
Kit comes in a convenient format, with 8-well strips precoated with histone H4 peptide substrate, reagents, and purified PRMT1 enzyme for 96 enzyme reactions.
Format

Catalog
Number


Component


Amount


Storage

51040

PRMT1 human recombinant enzyme

10 µg

-80°C












Avoid freeze/ thaw cycles!

52120

20 µM S-adenosylmethionine*

250 µl

-80°C

52150

Primary antibody 4

100 µl

-80°C

52131H

Secondary HRP-labeled antibody 2

10 µl

-80°C

52170

4x HMT assay buffer 2

3 ml

-20°C

52100

Blocking buffer 4

50 ml

+4°C

79670

ELISA ECL Substrate A
(transparent bottle)


6 ml


RT

79670

ELISA ECL Substrate B
(brown bottle)


6 ml


RT

 

96-well plate precoated with histone substrate

1 plate


+4°C

 

UniProt #
Q99873
Background
PRMT1 is a histone methyltransferase that exhibits methylation activity toward H4-R3.
References

Dillon S.C., et al. 2005. Genome Biology 6:227.