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Lipid Peroxide (LPO) Colorimetric Assay Kit

  • Cat.No.:E-BC-K176-M

  • Detection instrument: Microplate reader(580-590 nm)

To Purchase E-BC-K176-M

  • 96T
  • 48T
Price: $380

Detection principle

With 45℃ incubation for 60 min, one molecule of LPO react with two molecule of chromogenic reagent, to produce a stable chromophore which have the maximum absorption peak at 586nm. The content of LPO in samples can be calculated by standard curve or calculation formula.

Performance characteristics

Synonyms LPO
Sample type Serum,plasma,urine,tissue
Sensitivity 0.70 μmol/L
Detection range 0.70-80 μmol/L
Detection method Colorimetric method
Assay type Quantitative
Assay time 90 min
Precision Average inter-assay CV: 3.5%Average intra-assay CV: 3.1%
Other instruments required Water bath, Centrifuge, Micropipettor, Vortex mixer
Other reagents required Double distilled water, PBS (0.01 M, pH 7.4)
Storage 2-8℃
Valid period 6 months

Dilution of sample

It is recommended to take 2~3 samples with expected large difference to do pre-experiment before formal experiment and dilute the sample according to the result of the pre-experiment and the detection range ( 0.70-80 μmol/L).

The recommended dilution factor for different samples is as follows (for reference only):

Sample type

Dilution factor

Human serum


Human plasma




10% Rat kidney tissue homogenization


10% Rat liver tissue homogenization


Note: The diluent is PBS (0.01 M, pH 7.4).


From now on, if you have published a paper by using any of our products since 1/1/2019, fill out the “Elabscience Publication Reward Application Form”carefully and send it to, we will get back to you with the reward after we confirm it ASAP!

View more details about our Publication Reward >>

  1. Indian Journal of Forensic Medicine & Toxicology (2020)
    Reduced Glutathione, Lipid Peroxidation and Malondialdehyde Status in Women with Mild and Severe Preeclampsia for Babylon Governorate

    DOI: 10.37506/ijfmt.v14i1.144

    Sample: Serum


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