ELISA Kit for Brain Natriuretic Peptide (BNP)

ELISA CLIA Kits

2h

This assay has high sensitivity and excellent specificity for detection of Brain Natriuretic Peptide (BNP).

No significant cross-reactivity or interference between Brain Natriuretic Peptide (BNP) and analogues was observed.

The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.

To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.

This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to Brain Natriuretic Peptide (BNP) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled Brain Natriuretic Peptide (BNP) and unlabeled Brain Natriuretic Peptide (BNP) (Standards or samples) with the pre-coated antibody specific to Brain Natriuretic Peptide (BNP). After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of Brain Natriuretic Peptide (BNP) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of Brain Natriuretic Peptide (BNP) in the sample.