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Updated: Aug 19, 2026

Development and Validation of an Ultrasensitive Single Molecule Array Digital Enzyme-linked Immunosorbent Assay for Human Interferon-α
Published on: June 14, 2018
[Development of super-sensitive radical immunoassay for Cry j 1]
Masaaki Aoyama1, Yuichi Takahashi
1Institute for Life Support Technology. aoyama@yat.ymgt-techno.or.jp
Abstract:
We have been developed super-sensitive method of Cry j 1 measurement by ESR radical immunoassay using p-acetamidophenol and hydroxylamine system. The detection limit for Cry j 1 was 3.5 pg/ml. It is reported that the average content of Cry j 1 in each Cryptomeria japonica pollen is about 6 pg, therefore, we can detect one grain or even less one grain of the pollen by our method. It was possible to inform the useful information for sensitive C. japonica pollinosis patients before development their symptoms due to the super-sensitive measurement.
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Western Blotting
The technique begins with separating proteins from the sample using sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), followed by protein transfer, immunoblotting, and finally, protein detection.
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