Serum Acid Treatment

Serum acid treatment is a laboratory method that exposes serum to controlled low-pH conditions to selectively alter acid-sensitive components, helping researchers distinguish antibody activity from other serum effects in immunology and infection studies. Acidification can disrupt or inactivate complement and other labile proteins, while many immunoglobulins may retain sufficient activity for subsequent assays, depending on the pH and exposure time. Researchers use this treatment to prepare serum samples, assess complement dependence, investigate antibody-mediated neutralization, and clarify how host factors influence pathogen infection or immune responses. Careful control of treatment conditions is essential because excessive acidity can also damage antibodies and other proteins.

Serum Acid Treatment - Related Videos

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JoVE Journal - Bioengineering
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Treatment of Ligament Constructs with Exercise-conditioned Serum: A Translational Tissue Engineering Model

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Cited by 7 •

2017

We present a model of ligament tissue in which three-dimensional constructs are treated with the human exercise-conditioned serum and analyzed for collagen content, function, and cellular biochemistry.

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JoVE EoE - Assay Techniques

Thiobarbituric Acid-Reactive Substances Assay to Assess Oxidative Stress in Human Serum

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2025

This video demonstrates the thiobarbituric acid reactive substances (TBARS) assay to assess oxidative stress in biological samples.

Measuring Immunoglobulin G Levels Against a Test Vaccine in a Mouse Serum

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2025

This video demonstrates a method for assessing the antibody immune response to a novel nanoemulsion adjuvant vaccine in pre-immunized mice. Immunization enhances antibody response as confirmed by determining the IgG antibody titers.

Isolation of Small Noncoding RNAs from Human Serum

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Cited by 13 •

2014

This protocol describes a method for extracting small RNAs from human serum. We have used this method to isolate microRNAs from cancer serum for use in DNA arrays and also singleplex quantitative PCR. The protocol utilizes phenol and guanidinium thiocyanate reagents with modifications to yield high quality RNA.

Research

JoVE Journal - Biology
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Quantification of Endothelial Fatty Acid Uptake using Fluorescent Fatty Acid Analogs

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2025

This protocol details an in vitro assay for measuring cellular lipid uptake in endothelial cells upon stimulation with BODIPY-C12 and BODIPY-C16 fluorescent analogs of long-chain and very long-chain saturated fatty acids. This method is efficient and adaptable to other cell types, offering a useful approach for studying lipid metabolism.

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