2016
DOI: 10.1016/j.bios.2016.02.049
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A portable chemiluminescence imaging immunoassay for simultaneous detection of different isoforms of prostate specific antigen in serum

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Cited by 82 publications
(28 citation statements)
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“…Excess DTT and thiol fragments were removed from the mixture by extraction with ethyl acetate (three times, total volume of 150 µL), and the upper layer was discarded, the next step was then immediately performed. Immobilization of aptamer was done by dropping 10 μL of 10.0 μmol dm −3 aptamer solution dissolved in Tris on the HL-Au electrode surface and kept at 4 °C for 8 h 11 , 28 , 34 . Then, the electrode was rinsed with Tris, and further treated with 1.0 mmol dm −3 6-mercapto-1-hexanol at room temperature for 30 min to obtain a well aligned aptamer monolayer 11 , 28 , 34 .…”
Section: Methodsmentioning
confidence: 99%
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“…Excess DTT and thiol fragments were removed from the mixture by extraction with ethyl acetate (three times, total volume of 150 µL), and the upper layer was discarded, the next step was then immediately performed. Immobilization of aptamer was done by dropping 10 μL of 10.0 μmol dm −3 aptamer solution dissolved in Tris on the HL-Au electrode surface and kept at 4 °C for 8 h 11 , 28 , 34 . Then, the electrode was rinsed with Tris, and further treated with 1.0 mmol dm −3 6-mercapto-1-hexanol at room temperature for 30 min to obtain a well aligned aptamer monolayer 11 , 28 , 34 .…”
Section: Methodsmentioning
confidence: 99%
“…Immobilization of aptamer was done by dropping 10 μL of 10.0 μmol dm −3 aptamer solution dissolved in Tris on the HL-Au electrode surface and kept at 4 °C for 8 h 11 , 28 , 34 . Then, the electrode was rinsed with Tris, and further treated with 1.0 mmol dm −3 6-mercapto-1-hexanol at room temperature for 30 min to obtain a well aligned aptamer monolayer 11 , 28 , 34 . Then, the electrode was washed again with Tris and double distilled water, respectively, to remove non-specific adsorbed thiols.…”
Section: Methodsmentioning
confidence: 99%
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“…This immunoassay of serum samples displayed high sensitivity. 29 Determination of the Oxidative Production and Antioxidative Enzymes…”
Section: Measurement Of the Ctnt And Ctni Levelsmentioning
confidence: 99%
“…Up to now, a lot of methods and tools have been proposed for determination of PSA including fluorescence [30,31], surface enhanced Raman scattering (SERS) [32], surface plasmon resonance [33,34], field-effect transistors [35], capillary electrophoresis [36], white-light reflectance spectroscopy [37], mass spectrometry [38], lateral flow [39], electrochemical [40][41][42][43][44][45], chemiluminescence and electrochemiluminescence [46][47][48][49][50][51][52][53], ELISA and immunoassay [54][55][56], and a point-ofcare detection chip [57]. PSA detection in the blood by most of these methods includes routine immunoassays.…”
mentioning
confidence: 99%