2021
DOI: 10.1016/j.talanta.2020.121818
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Aptamer selection and aptasensor construction for bone density biomarkers

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Cited by 16 publications
(7 citation statements)
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“…The electrodes were rinsed with DI water to remove the excess aptamers and, finally, incubated with 0.5% of BSA to ensure specific binding. Due to this blocking step, the recorded signal can be ascribed only to the interaction between aptamers and the analyte [ 47 ]. Finally, the electrodes were rinsed with DI water and kept in the refrigerator at 4 °C when not in use.…”
Section: Methodsmentioning
confidence: 99%
“…The electrodes were rinsed with DI water to remove the excess aptamers and, finally, incubated with 0.5% of BSA to ensure specific binding. Due to this blocking step, the recorded signal can be ascribed only to the interaction between aptamers and the analyte [ 47 ]. Finally, the electrodes were rinsed with DI water and kept in the refrigerator at 4 °C when not in use.…”
Section: Methodsmentioning
confidence: 99%
“…It has been widely used to recognize various targeted sites, such as small molecules of antibiotics, short peptides, metal ions, and organic dyes, as well as a wide variety of proteins with complex multimeric structures, also including cells, viruses, and bacteria ( Wang et al, 2015 ). Aptamers have been used for diagnosis, detection, and targeted therapy due to their easy acquisition and great targeting ability ( Chinnappan et al, 2021 ). In addition, the high stability of aptamers, their low toxicity and immunogenicity, and their chemical modification to confer controlled or periodic denaturation and renaturation have expanded the flexibility of aptamer use in various biomaterials ( Ye et al, 2012 ).…”
Section: Bone-targeted Strategiesmentioning
confidence: 99%
“…Aptamers can bind to highly toxic or non-immunogenic antigens, an attribute that cannot be achieved with animal-based methods of mAb production. Aptamers are intermediate in size (8)(9)(10)(11)(12)(13)(14)(15)) between antibodies (150 kDa) and small peptides (1-5 kDa), and about 20 times smaller than antibodies [3]. Their small size can lead to better tissue penetration, which can be used in solid tumor therapy.…”
Section: Monoclonal Antibodies Aptamersmentioning
confidence: 99%
“…During the SELEX process, the target molecules are immobilized on a solid support (e.g., chromatographic beads or sepharose beads) to facilitate the separation of targetbinding oligonucleotides from non-binding ones. The ssDNA library pool of 10 15 random nucleotide sequences are incubated with immobilized target molecule and the enrichment in the ssDNA binding aptamer is monitored by the fluorescence [9]. SELEX can be performed against the purified protein as well as against whole cells by cell-SELEX, and the ssDNA/RNA aptamers bind to specific cell membrane proteins existing on live cells.…”
Section: Aptamer Selection Technologymentioning
confidence: 99%