TET2 Chemiluminescent Assay Kit

Catalog #
50652
$760 *
Size: 96 reactions
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Description

The TET2 Chemiluminescent Assay Kit is designed to measure TET2 activity for screening and profiling applications. TET2 belongs to the Ten Eleven Translocation (TET) family proteins that catalyze 5-methylcytosine oxidation and generate 5-methylcytosine derivatives, including 5-hydroxymethylcytosine. TET2 is one of the most frequently mutated genes in myeloid malignancies.

The key to the TET2 Chemiluminescent Assay Kit is a highly specific antibody that recognizes hydroxymethylated substrate. With this kit, only three simple steps on a microtiter plate are required for detection of TET2 activity. First, TET2 enzyme is incubated with the methylated substrate for two hours. Then the primary antibody is added. Next, the plate is treated with an HRP-labeled secondary antibody. Finally, the HRP substrate is added to produce chemiluminescence that can be measured using a chemiluminescence reader.

Need us to run inhibitor screens or profile your compounds against TET2? Check out our Demethylase Screening Services

Synonyms
Ten-eleven translocation 2 protein, methylcytosine dioxygenase TET2
Product Info
Storage and Usage
Citations
Assay Kit Format
Chemiluminescent
Supplied As
The TET2 Chemiluminescent Assay Kit comes in a convenient format; a 96-well strip plate precoated with methylated DNA substrate, primary antibody, a secondary HRP-labeled antibody, TET2 assay buffer, and purified TET2 for 100 enzyme reactions.
Format

 

Catalog Number
Component 

Amount

Storage
50162 TET2 40 µg -80°C  Avoid
multiple
freeze/
thaw
cycles!
52140Z2 Primary antibody 27 100 µl -80°C
52131H Secondary HRP-labeled antibody 2 10 µl -80°C
79832 4x TET2 assay buffer 1 3 ml -80°C
52100 Blocking buffer 4 50 ml +4°C
79670 ELISA ECL Substrate A (transparent bottle) 6 ml Room Temp.
79670 ELISA ECL Substrate B (brown bottle) 6 ml Room Temp.
  8-well strip plate module precoated with DNA substrate 1 +4°C
UniProt #
Q6N021
References

Li Tan, Yujiang Geno Shi. Development 2012; 139(11): 1895-1902.