2019
DOI: 10.1016/j.talanta.2019.05.057
|View full text |Cite
|
Sign up to set email alerts
|

Target-catalyzed hairpin structure-mediated padlock cyclization for ultrasensitive rolling circle amplification

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
4
0

Year Published

2020
2020
2024
2024

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 12 publications
(4 citation statements)
references
References 60 publications
0
4
0
Order By: Relevance
“…This study was conducted using target-catalyzed hairpin structure-mediated padlock cyclization for the ultrasensitive detection of human proto-oncogenes. Here, the author described THP-RCA that could be performed in human serum conditions along with a detection limit of 100 fM . Nucleic acid fluorescent probe engineering has been vastly studied in recent times, and the involvement of fluorophores and chemically modified linkage in molecular diagnostics have been unraveled significantly since the fluorophore utilization/conjugation interest the use of functional nanomaterials to explore their intrinsic properties for DNA/nucleic acid sensing. , …”
Section: Dna Probe-designed Nucleic Acid Detectionmentioning
confidence: 99%
“…This study was conducted using target-catalyzed hairpin structure-mediated padlock cyclization for the ultrasensitive detection of human proto-oncogenes. Here, the author described THP-RCA that could be performed in human serum conditions along with a detection limit of 100 fM . Nucleic acid fluorescent probe engineering has been vastly studied in recent times, and the involvement of fluorophores and chemically modified linkage in molecular diagnostics have been unraveled significantly since the fluorophore utilization/conjugation interest the use of functional nanomaterials to explore their intrinsic properties for DNA/nucleic acid sensing. , …”
Section: Dna Probe-designed Nucleic Acid Detectionmentioning
confidence: 99%
“…In the integration of RCA with CHA, two common ways were chosen, including CHA product as RCA primer (CHA-RCA) [ [105] , [106] , [107] , [108] ] and RCA product as CHA trigger (RCA-CHA) [ 109 , 110 ]. In addition, a nicking enzyme was used in RCA-CHA to deal with the problem of hindering the initiation of CHA by RCA products [ 111 ].…”
Section: Semi-enzyme-free Cascade Amplificationmentioning
confidence: 99%
“…Then, HP2 is cyclized by ligase on the HP1 template; the cyclized HP2 enables the RCA and generates a long tandem ssDNA product that is capable of hybridizing with considerable quantity of MBs. Subsequently, the amplified fluorescence value represents the ultrasensitive detection of STAT3 gene ( Song et al, 2019 ). Moreover, the sensing system is suitable for target detection in human serum.…”
Section: The Application Of Nucleic Acid Probe–based Fluorescent Sensing In Cancer Diagnosis and Treatmentmentioning
confidence: 99%