Published TCIMAIL newest issue No.196
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Peroxidase Detection
No.164(January 2015)
Chemiluminescence has contributed to providing high sensitivity for enzyme-linked immunoassays.1,2) Thorpe et al. referred that, when peroxidase is used for immunoassay as a labeled enzyme, hydrogen peroxide can be replaced by oxidants such as perborate.2) Compound 1 is the sodium salt of perborate. In their study,3) they used the sodium salt to replace hydrogen peroxide. 1 has already been employed for recent improvements of immunoassay.4,5)
On the other hand, interestingly, 1 has already been used as a substrate of catalase in the late 1940’s.6)
References
- 1)Chemiluminescent enzyme immunoassay, a review
- 2)Enhanced chemiluminescence enzyme immunoassay
- 3)Phenols as enhancers of the chemiluminescent horseradish peroxidase–luminol–hydrogen peroxide reaction: Application in luminescence-monitored enzyme immunoassays
- 4)Inhibition of horseradish peroxidase (HRP) by a nonhydrophobic component of urine: A caution for immunoassays
- 5)Development of a highly sensitive chemiluminescence enzyme immunoassay using enhanced luminol as substrate
- 6)Perborate as substrate in a new assay of catalase
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