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Instructions for Surfactant Protein D ELISA Enzyme immunoassay for the quantitative determination of human Surfactant Protein D in serum, plasma, bronchoalveolar lavage fluid or amniotic fluidBV53041 12
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01
Prepare the samples and standards.
02
Coat the plate with the capture antibody.
03
Block the plate to prevent non-specific binding.
04
Add the samples, standards, and detection antibody.
05
Add the substrate solution and incubate in the dark.
06
Stop the reaction and measure the absorbance.
07
Calculate the concentrations using a standard curve.

Who needs elisa technique for quantification?

01
Researchers studying protein quantification in biological samples.
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Laboratories performing diagnostic tests for various diseases.
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Scientists investigating biomarkers for research purposes.
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The ELISA (Enzyme-Linked Immunosorbent Assay) technique is a biochemical assay used to detect and quantify proteins, antibodies, hormones, or other molecules in a sample through a specific antigen-antibody interaction.
Individuals or organizations conducting research, clinical trials, or diagnostic tests that involve the use of ELISA assays are typically required to file the technique, depending on the regulations of their respective field or region.
To fill out the ELISA technique for quantification, one must provide details such as the sample type, assay design, reagents used, standard curve data, and results interpretation according to the guidelines set by relevant regulatory bodies.
The purpose of the ELISA technique for quantification is to provide a reliable and reproducible method for measuring the concentration of specific antigens or antibodies in a variety of samples, aiding in diagnosis, research, and quality control.
The information that must be reported typically includes assay methodology, sample details, quantitative results, standard curve, positive and negative controls, and any troubleshooting performed during the process.
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