a-Fetoprotein in sera from healthy subjects and patients with liver cirrhosis and hepatocellular carcinoma was fractionated into three peaks by affinity chromatography on a column of Lens culinaris agglutinin-Sepharose 48. One peak (the first peak) was found in all the serum samples, but the other t
Application of a mimetic enzyme for the enzyme immunoassay for α-1-fetoprotein
✍ Scribed by Ci Yun-Xiang; Qin Yang; Chang Wen-Bao; Li Yuan-Zong
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 295 KB
- Volume
- 300
- Category
- Article
- ISSN
- 0003-2670
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✦ Synopsis
A new mimetic enzyme immunoassay (MEIA) method for cY-1-fetoprotein (AFP) was developed using a mimetic enzyme Mn( III)-tetra( suIfophenyl)porphine (Mn-TPPS,) as a labelling reagent to catalyze the fluorescence reaction of 4-hydroxyphenylacetic acid (HPA) and hydrogen peroxide. In the sandwich assay standard AFP solution or AFP containing umbilical blood serum Crst reacts with antibody (anti-AFP) coated on a 40-well plate (polystyrene), and then further reacts with Mn-TPPS,-labelled anti-AFP; the Mn-TPP& on the bound fraction, after removing the free fraction was determined by measuring the fluorescence intensity as a result of the reaction between HPA and H202, catalyzed by bound Mn-TPPS, and anti-AFP conjugate, which was proportional to the concentration of AFP. AFT in the range 0.01-10 pg per well can be determined with a detection limit of 1 ng per well. The method has sufficient sensitivity to be applied to the determination of AFP in umbilical blood serum.
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