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
Documents
Frequently Asked Questions
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