2018
DOI: 10.1039/c8sc02752h
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An ultrasensitive flow cytometric immunoassay based on bead surface-initiated template-free DNA extension

Abstract: An ultrasensitive flow cytometric immunoassay (TdT-FCI) is developed based on bead surface-initiated template-free DNA extension.

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Cited by 36 publications
(26 citation statements)
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“…[ 50 ] LSRP results from strong localized electromagnetic fields that exhibited at metal nanostructures, which can realize sensitive detection of nanoscale biological analysts. [ 51 ] Thakur et al. developed a self‐assembly gold nanoislands (AuNIs) sensing chip combined with the LSPR biosensor to detect and differentiate exosomes from microvesicles (MVs) isolated from cells and real samples without antibody functionalization.…”
Section: Exosome Detection Methodologiesmentioning
confidence: 99%
“…[ 50 ] LSRP results from strong localized electromagnetic fields that exhibited at metal nanostructures, which can realize sensitive detection of nanoscale biological analysts. [ 51 ] Thakur et al. developed a self‐assembly gold nanoislands (AuNIs) sensing chip combined with the LSPR biosensor to detect and differentiate exosomes from microvesicles (MVs) isolated from cells and real samples without antibody functionalization.…”
Section: Exosome Detection Methodologiesmentioning
confidence: 99%
“…35 Isothermal amplication of nucleic acids (e.g., rolling circle amplication (RCA)) as an alternative amplication technique enables rapid and effective amplication at constant temperature. [35][36][37][38][39][40][41][42][43][44] RCA may generate very long single-stranded DNAs (ssDNAs) with tandem repeats, and it can achieve approximately 10 3 -fold amplication within 1 h. 35,[45][46][47] The visualization and analysis of RCA products usually use either SYBR green I as the uorescence label 45 or the uorescence-labeled oligonucleotide probe. 46 SYBR Green I is a DNA intercalating dye that binds dsDNA, 45 but it has several limitations including the concentration-dependent inhibition of PCR, preferential binding to the GC-rich sequences, the promotion of nonspecic amplication, and the detection of only a single type of target due to the use of a single uorophore, false positive signals due to its binding to any dsDNAs including nonspecic dsDNA sequences.…”
Section: Introductionmentioning
confidence: 99%
“…Owing to the high stability, low cost, and convenient labeling, nanoparticles can also serve as signal probes for DNA detection to further improve the performance of sandwich assays [106][107][108][109][110][111][112][113][114][115]. For example, Zhang et al [116] reported a nanoparticle based "sandwich" detection strategy by immobilizing gold nanoparticles (AuNPs) with reporter probes that flank the target nucleic acids.…”
Section: +mentioning
confidence: 99%