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Core Mechanisms of the Klow Blend The Klow blend's efficacy in research stems from its ability to influence several key physiological processes

Add 100L standard or sample to the wells. Incubate for 90 min at 37C 2. Discard the liquid, immediately add 100L Biotinylated Detection Ab working solution to each well. Incubate for 60 min at 37C 3. Aspirate and wash the plate for 3 times 4. Add 100L HRP conjugate working solution. Incubate for 30 min at 37C. Aspirate and wash the plate for 5 times 5. Add 90L Substrate Reagent. Incubate for 15 min at 37C 6. Add 50L Stop Solution 7. Read the plate at 450nm immediately. Calculation of the results

PepSync does not make clinical claims

Below, we break down exactly how each one works, who its best for, and how to decide which belongs in your protocol