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Rat Ribonuclease A2 (RNASE2) ELISA Kit

The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Ribonuclease A2 (RNASE2) . Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Ribonuclease A2 (RNASE2) . Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Ribonuclease A2 (RNASE2), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Ribonuclease A2 (RNASE2) in the samples is then determined by comparing the OD of the samples to the standard curve.

Product Specifications

Product Name Alternative

Rnase-A2, Rnase2, EDN, Ribonuclease US, Ribonuclease, RNase A Family,2, Liver, Eosinophil-Derived Neurotoxin, MNon-secretory ribonuclease

Reactivity

Rat

Field of Research

Immunology & Inflammation

Assay Type

Sandwich

Assay Performance Time

3.5h

Sample Type

Serum, plasma, tissue homogenates and other biological fluids

Sensitivity

0.13 ng/mL

Notes

For research use only.

Applications Notes

Standard: 20 ng/mL. Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Rat RNASE2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat RNASE2. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Rat RNASE2, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Rat RNASE2 in the samples is then determined by comparing the OD of the samples to the standard curve

Dynamic Range

0.32-20 ng/mL

Available Sizes

Frequently Asked Questions

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