2015
DOI: 10.1016/j.bios.2015.01.042
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SPAD aptasensor for the detection of circulating protein biomarkers

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Cited by 27 publications
(8 citation statements)
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“…Therefore, the long‐term stability of the proposed aptamer sensor was evaluted by measuring the response of 2.0 pM TB twice in a week for two months. For the regeneration of the sensor surface after each measurement, the aptamer sensor was dipped into a 0.2 M glycine‐hydrochloric acid (Gly‐HCl) buffer solution (pH=2.8) for 5 min 51. After three times washing with a HEPES solution, the aptamer sensor was incubated in the mixture of 2.0 pM TB and 16 μg/mL of TB/AuNPs/MB conjugate solutions.…”
Section: Resultsmentioning
confidence: 99%
“…Therefore, the long‐term stability of the proposed aptamer sensor was evaluted by measuring the response of 2.0 pM TB twice in a week for two months. For the regeneration of the sensor surface after each measurement, the aptamer sensor was dipped into a 0.2 M glycine‐hydrochloric acid (Gly‐HCl) buffer solution (pH=2.8) for 5 min 51. After three times washing with a HEPES solution, the aptamer sensor was incubated in the mixture of 2.0 pM TB and 16 μg/mL of TB/AuNPs/MB conjugate solutions.…”
Section: Resultsmentioning
confidence: 99%
“…Luminescence, as a general term is related to the energy transition between molecular orbitals that produces an emission of light. When the excitation of the molecules is caused by a chemical reaction, this light emission is chemiluminescence [ 27 , 33 , 36 , 58 , 71 , 81 ]. The emission that accompanies an electrochemical reaction is known as electrochemiluminescence [ 79 ].…”
Section: Detection Methods and Assay Formatsmentioning
confidence: 99%
“…The Fab′ were immobilized on the Si 3 N 4 surface adapting the protocol described in Yoshimoto et al ., [ 11 ] with some modifications. In order to introduce thiol groups able to react with the cysteine groups on Fab′ fragments, the silicon nitride surface was functionalized in wet conditions with mercaptosilane (MPTMS) [ 12 ]. The surfaces (both aMZI chip and flat samples) were cleaned with an argon plasma (6.8 W, one min) to remove organic contaminants and to hydroxylate the surface and were then immersed in a 1% v/v solution of MPTMS in toluene anhydrous at 60 °C for 10 min.…”
Section: Methodsmentioning
confidence: 99%