Immunoaffinity chromatography of abscisic acid combined with electrospray liquid chromatography-mass spectrometry
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
17064969
DOI
10.1016/j.jchromb.2006.09.034
PII: S1570-0232(06)00803-8
Knihovny.cz E-resources
- MeSH
- Chromatography, Affinity methods MeSH
- Chromatography, Liquid methods MeSH
- Enzyme-Linked Immunosorbent Assay methods MeSH
- Spectrometry, Mass, Electrospray Ionization methods MeSH
- Abscisic Acid analysis chemistry immunology MeSH
- Plant Leaves chemistry drug effects metabolism MeSH
- Reproducibility of Results MeSH
- Nicotiana chemistry drug effects metabolism MeSH
- Water metabolism pharmacology MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Abscisic Acid MeSH
- Water MeSH
Polyclonal antibodies with high specificity for C1-immobilised (+)-cis,trans-abscisic acid (ABA) were raised, characterised by enzyme-linked immunosorbent assay (ELISA) and used for preparation of an immunoaffinity chromatography (IAC) gel. The detection limit of the ELISA was approximately 4.6x10(-10)mol/L. Sensitive electrospray liquid chromatography-mass spectrometry (LC-ESI-MS) methods were also developed with detection limits below 0.1x10(-12)mol. The IAC allowed quick, single-step processing of samples prior to the analyses. The LC-ESI-MS and LC-ELISA techniques were used for comparative estimation of endogenous ABA levels in immunoaffinity purified extracts of normal and water-stressed Nicotiana tabacum L. leaves. The analytical approaches were validated using deuterium- and tritium-labelled internal standards, respectively. The IAC method was found to be highly effective, sensitive and convenient for isolating the target analyte from plant material.
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