Ab108796 Angiotensin II Human ELISA Kit - Abcam
ab108796
Angiotensin II Human ELISA Kit
Instructions for Use
For the quantitative measurement of Human Angiotensin II concentrations in plasma, serum and cell culture supernatants This product is for research use only and is not intended for diagnostic use.
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Table of Contents
1. Introduction
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2. Assay Summary
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3. Kit Contents
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4. Storage and Handling
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5. Additional Materials Required
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6. Preparation of Reagents
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7. Assay Method
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8. Data Analysis
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9. Specificity
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10. Troubleshooting
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1. Introduction
Angiotensin II (ANG-II), a main effector peptide in the reninangiotensin system, acts as a growth promoting and angiogenic factor via type-1 Angiotensin II receptors. Angiotensin II is thought to be involved in the regulation of cell proliferation, angiogenesis, inflammation and cancer.
ab108796 Angiotensin II Human ELISA kit is designed for detection of human Angiotensin II in plasma, serum, and cell culture supernatants. This assay employs a quantitative sandwich enzyme immunoassay technique that measures Angiotensin II in less than 5 hours. A polyclonal antibody specific to Angiotensin II has been pre-coated onto a microplate. The Angiotensin II in standards and samples is sandwiched by the immobilized antibody and biotinylated polyclonal antibody specific to Angiotensin II, which is recognized by a streptavidin-peroxidase conjugate. All unbound material is then washed away and a peroxidase enzyme substrate is added. The color development is stopped and the intensity of the color is measured.
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2. Assay Summary
Prepare all reagents, samples and standards as instructed. Add 50 ?l standard or sample to each well. Incubate 2 hours at room temperature. Wash the microplate 5 x with wash buffer.
Add 50 ?l prepared biotin antibody to each well. Incubate 2 hours at room temperature.
Wash the microplate 5 x with wash buffer. Add 50 ?lof Streptavidin-Peroxidase Conjugate.
Incubate 30 minutes at room temperature. Wash the microplate 5 x with wash buffer. Add 50 ?l of Chromogen Substrate to each well. Incubate 20 minutes or till the optimal blue colour density develops. Add 50 ?l Stop Solution to each well. Read at 450 nm immediately.
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