ELISA/assay

N-Terminal Pro-Brain Natriuretic Peptide (NT-ProBNP) ELISA Kit

MBS2020035

24-Strip-Wells

305 USD

ELISA Kit

N-Terminal Pro-Brain Natriuretic Peptide (NT-ProBNP) ELISA Kit

[N-Terminal Pro-Brain Natriuretic Peptide (NT-ProBNP)]

[NT-Pro-BNP; ; N-BNP]

[NT-ProBNP]

Rat

This assay has high sensitivity and excellent specificity for detection of N-Terminal Pro-Brain Natriuretic Peptide (NT-ProBNP). No significant cross-reactivity or interference between N-Terminal Pro-Brain Natriuretic Peptide (NT-ProBNP) 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.

Typical Testing Data/Standard Curve

Assay Type: Competitive Inhibition. Samples: Serum, Plasma, Tissue homogenates, Cell lysates, Cell culture supernates and Other Biological Fluids. Detection Range: 123.5-10,000pg/mL. Sensitivity: < 49.9pg/mL

Application: Enzyme-linked immunosorbent assay for Antigen Detection. Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level N-Terminal Pro-Brain Natriuretic Peptide (NT-ProBNP) were tested 20 times on one plate, respectively. Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level N-Terminal Pro-Brain Natriuretic Peptide (NT-ProBNP) were tested on 3 different plates, 8 replicates in each plate. CV(%) =: SD/meanX100. Intra-Assay: CV<10%. Inter-Assay: CV<12%

Endocrinology; Cardiovascular biology

This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to N-Terminal Pro-Brain Natriuretic Peptide (NT-ProBNP) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled N-Terminal Pro-Brain Natriuretic Peptide (NT-ProBNP) and unlabeled N-Terminal Pro-Brain Natriuretic Peptide (NT-ProBNP) (Standards or samples) with the pre-coated antibody specific to N-Terminal Pro-Brain Natriuretic Peptide (NT-ProBNP). 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 N-Terminal Pro-Brain Natriuretic Peptide (NT-ProBNP) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of N-Terminal Pro-Brain Natriuretic Peptide (NT-ProBNP) in the sample.

24-Strip-Wells

305 USD

48-Strip-Wells

575

96-Strip-Wells

780

5x96-Strip-Wells

3175

10x96-Strip-Wells

5730