SUV39H1 Chemiluminescent Assay Kit

Catalog #
52006L
$750 *
Size: 96 reactions
Qty
*US Pricing only. For international pricing, please contact your local distributor.
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Description

The SUV39H1 Chemiluminescent Assay Kit is designed to measure SUV39H1 activity for screening and profiling applications. The key to the SUV39H1 Chemiluminescent Assay Kit is a highly specific antibody that recognizes methylated K9 residue of Histone H3. 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 plate is treated with an HRP-labeled secondary antibody followed by addition of the ELISA ECL substrate to produce chemiluminescence that can then be measured using a chemiluminescence reader.

Synonyms
KMT1A, SUV39H1, Suppressor Of Variegation 3-9 Homolog 1 (Drosophila), Su(Var)3-9 Homolog 1
Product Info
Storage and Usage
Citations
Assay Kit Format
Chemiluminescent
Supplied As
The SUV39H1 Chemiluminescent Assay Kit comes in a convenient format, with a 96-well strip plate precoated with histone H3 peptide substrate, primary antibody against methylated lysine residue of Histone H3, secondary HRP-labeled antibody, S-adenosylmethionine, methyltransferase assay buffer, and purified SUV39H1 enzyme for 96 enzyme reactions.
Format
Catalog # Component Amount Storage
51070 SUV39H1 human enzyme* 10 µg -80°C Avoid freeze/thaw cycles!
52120 100 µM S-adenosylmethionine 250 µl -80°C
52140A Primary antibody 1 100 µl -80°C
52130H Secondary HRP-labeled antibody 1 10 µl -80°C
52160 4x HMT assay buffer 1 3 ml -20°C
79556 Blocking buffer 1 50 ml +4°C
79670

ELISA ECL substrate A (transparent bottle)

6 ml Room Temp.
ELISA ECL substrate B (brown bottle) 6 ml Room Temp.
  96-well strip plate precoated with histone substrate 1 plate +4°C

*The concentration of SUV39H1 is lot-specific and will be indicated on the tube containing the enzyme.

UniProt #
O43463
References
Dillon S.C., et al. 2005. Genome Biology 6:227.