Overview
- Product namePhosphatidylcholine Assay Kit
- Tests100 x 1 assay
- Sample typeCell culture supernatant, Urine, Serum, Plasma, Other biological fluids, Tissue Extracts
- Assay typeQuantitative
- Sensitivity> 0.2 mM
- Range0.2 mM - 2.5 mM
- Assay time0h 40m
- Product overview
Abcam's Phosphatidylcholine Assay Kit is a simple convenient means of measuring Phosphatidylcholine in a variety of biological samples. The kit utilizes an enzyme-coupled assay in which PC is hydrolyzed, releasing choline which is subsequently oxidized resulting in development of the OxiRed probe to generate fluorescence (Ex/Em 535 nm 587 nm) and absorbance (570 nm). Abcam's Phosphatidylcholine Kit measures PC in the range of 0.1 to 10 nmol per sample. PC is present in serum at ~0.2-2.5 mM (~50-200 mg/dL).
Visit our FAQs page for tips and troubleshooting. - Notes
Phosphatidylcholine (PC) is a phospholipid which incorporates choline as the headgroup of the lipid. PC is a major constituent of biological membranes and is involved in cell signaling through release of choline by phospholipase D leaving the second messenger phosphatidic acid.
- Tested applicationsFunctional Studies more details
Properties
- Storage instructionsStore at -20°C. Please refer to protocols.
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Components Identifier 100 tests OxiRed Probe in DMSO Red 1 x 200µl PC Assay Buffer WM 1 x 25ml PC Development Mix (Lyophilised) Green 1 vial PC Hydrolysis Enzyme (lyophilized) Purple 1 vial PC Standard (10 µmol) (Lyophilised) Yellow 1 vial -
Research Areas
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Alternative names
- PC
Applications
Our Abpromise guarantee covers the use of ab83377 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
| Application | Notes |
|---|---|
| Functional Studies | FuncS |
Phosphatidylcholine Assay Kit images
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Examples of Colorimetric and Fluorometric Phosphatidylcholine standard curves using ab83377.
Protocols
References for Phosphatidylcholine Assay Kit (ab83377)
ab83377 has not yet been referenced specifically in any publications.
