CheKine™ Micro Hydroxyl Free Radical Scavenging Capacity Assay Kit

• Ferrous Salt
• H2O2
•Salicylic Acid
• Free-HSA Negative Control

• Do not mix the components between different batch numbers and manufacturers, otherwise, the results may be abnormal.
• Avoid bubbles while mixing or redissolving components.
• Change pipette tips frequently to avoid cross contamination between components.
• Ensure that all components and equipment are at the proper temperature before starting the experiment.
• In order to guarantee the accuracy of experimental results, need to do a pre-experiment with 1-2 samples.
• If the OD value exceeds 1.3, the sample needs to be diluted.
• The sample is hemolyzed or has a dark color and needs to be compared with itself. The specific method is to add 200 µL of the diluted sample and 30 µL of Extraction Buffer (1x) to UV microplate, incubate at 37°C for 5 min, record the absorbance at 340 nm, and subtract the OD value of the self-control from the measurement well during calculation.
• Serum, plasma and tissue samples are recommended to be diluted 5 times with Extraction Buffer (1x) for testing.
• The Reagent I and Reagent II are stored in sealed condition.

The product listed herein is for research use only and is not intended for use in human or clinical diagnosis. Suggested applications of our products are not recommendations to use our products in violation of any patent or as a license. We cannot be responsible for patent infringements or other violations that may occur with the use of this product.

KTB1091-B.pdf

CheKine™ Micro Hydroxyl Free Radical Scavenging Capacity Assay Kit (Salicylic Acid Method) is specially developed for the detection of Hydroxyl Free Radical Scavenging Capacity in various sample such as plasma, serum, bacteria, animal /plant tissues and cells and other biological fluids.