ELISA Kit for Brain Natriuretic Peptide (BNP)

GC-B; B-Type Natriuretic Peptide; Ventricular Natriuretic Peptide; Gamma-brain natriuretic peptide; Brain natriuretic peptide 32

  • ELISA Kit for Brain Natriuretic Peptide (BNP)Packages (Simulation)
  • ELISA Kit for Brain Natriuretic Peptide (BNP)Packages (Simulation)
  • ELISA Kit for Brain Natriuretic Peptide (BNP)Results demonstration
  • CEA541Hu.jpgTypical Standard Curve
  • CertificateISO9001: 2008, ISO13485: 2003 Registered

Specificity of the ELISA Kit for Brain Natriuretic Peptide (BNP)

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.

Recovery of the ELISA Kit for Brain Natriuretic Peptide (BNP)

Matrices listed below were spiked with certain level of recombinantBrain Natriuretic Peptide (BNP) and the recovery rates were calculated by comparing the measured value to the expected amount of Brain Natriuretic Peptide (BNP) in samples.

MatrixRecovery range (%)Average(%)
serum(n=5)84-9991
EDTA plasma(n=5)81-104101
heparin plasma(n=5)81-9387

Precision of the ELISA Kit for Brain Natriuretic Peptide (BNP)

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Brain Natriuretic Peptide (BNP) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Brain Natriuretic Peptide (BNP) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%

Linearity of the ELISA Kit for Brain Natriuretic Peptide (BNP)

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Brain Natriuretic Peptide (BNP) and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.

Sample1:21:41:81:16
serum(n=5)80-97%80-98%84-101%85-92%
EDTA plasma(n=5)81-94%93-101%80-92%80-93%
heparin plasma(n=5)80-89%80-103%96-105%95-103%

Stability of the ELISA Kit for Brain Natriuretic Peptide (BNP)

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.

Reagents and materials provided of the ELISA Kit for Brain Natriuretic Peptide (BNP)

ReagentsQuantityReagentsQuantity
Pre-coated, ready to use 96-well strip plate1Plate sealer for 96 wells4
Standard2Standard Diluent1×20mL
Detection Reagent A1Assay Diluent A1×12mL
Detection Reagent B1×120µLAssay Diluent B1×12mL
Reagent Diluent1×300µLStop Solution1×6mL
TMB Substrate1×9mLInstruction manual1
Wash Buffer (30 × concentrate)1×20mL

Assay procedure summary of the ELISA Kit for Brain Natriuretic Peptide (BNP)

1. Prepare all reagents, samples and standards;
2. Add 50µL standard or sample to each well.
    And then add 50µL prepared Detection Reagent A immediately.
    Shake and mix. Incubate 1 hour at 37°C;
3. Aspirate and wash 3 times;
4. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;
5. Aspirate and wash 5 times;
6. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;
7. Add 50µL Stop Solution. Read at 450 nm immediately.

ELISA Kit for Brain Natriuretic Peptide (BNP)

Test principle of the ELISA Kit for Brain Natriuretic Peptide (BNP)

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.

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