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Histamine ELISA [CE]

In the first part of the procedure,Histamineis quantitatively acylated to N-acyl histamine.The subsequent competitive ELISA uses the microtiter plate format. The antigen is bound to the solid phase of the microtiter plate. The acylated standards, controls and samples compete with the solid phase bound analytes for a fixed number of antibody binding sites.After the system is in equilibrium, free antigen and free antigen-antibody complexes are removed by washing. The antibody bound to the solid ph

Product Specifications

Certification

CE-IVD

Label

HRP

Type

ELISA

Sample Type

Urine, Plasma

Sample Volume

25 µL plasma 10µL urine

Detection Range

Urine : 0.91 – 125 ng/ml Plasma : 0.32 – 50 ng/ml

Sensitivity

Urine : 0.19 ng/ml Plasma : 0.12 ng/ml

Format

ELISA

Shelf Life

60 Weeks

Incubation Time

5h at RT with shaking 600 rpm

Disease

Biogenic Amines and Neurosciences

Marker

Histamine

Controls

2 levels

Frequently Asked Questions

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