scholarly journals Genotyping by Alkaline Dehybridization Using Graphically Encoded Particles

2011 ◽  
Vol 17 (10) ◽  
pp. 2867-2873 ◽  
Author(s):  
Huaibin Zhang ◽  
Adam J. DeConinck ◽  
Scott C. Slimmer ◽  
Patrick S. Doyle ◽  
Jennifer A. Lewis ◽  
...  
Keyword(s):  
Encoded Particles

Highly Controlled Silica Coating of PEG-Capped Metal Nanoparticles and Preparation of SERS-Encoded Particles†

Langmuir ◽  
2009 ◽  
Vol 25 (24) ◽  
pp. 13894-13899 ◽  
Author(s):  
Cristina Fernández-López ◽  
Cintia Mateo-Mateo ◽  
Ramón A. Álvarez-Puebla ◽  
Jorge Pérez-Juste ◽  
Isabel Pastoriza-Santos ◽  
...  
Keyword(s):  
Metal Nanoparticles ◽  
Silica Coating ◽  
Encoded Particles

scholarly journals Modular assembly of plasmonic core–satellite structures as highly brilliant SERS-encoded nanoparticles

2019 ◽  
Vol 1 (1) ◽  
pp. 122-131 ◽  
Author(s):  
Nicolas Pazos-Perez ◽  
Jamie M. Fitzgerald ◽  
Vincenzo Giannini ◽  
Luca Guerrini ◽  
Ramon A. Alvarez-Puebla
Keyword(s):  
Particle Loading ◽  
Modular Assembly ◽  
Homogeneous Core ◽  
Maximum Particle ◽  
Encoded Particles

Herein, we present a fabrication approach that produces homogeneous core–satellite SERS encoded particles with minimal interparticle gaps (<2–3 nm) and maximum particle loading, while positioning the encoding agents at the gaps.

A New Bio-Molecules Decryption Protocol Using Shape Encoded Particles (SEP)

2006 ◽  
Author(s):  
Jane Gin Fai Tsai ◽  
Zugen Chen ◽  
B. Merriman ◽  
J. Chen ◽  
S. Nelson ◽  
...  
Keyword(s):  
Encoded Particles

Multifunctional Encoded Particles for High-Throughput Biomolecule Analysis

Science ◽  
2007 ◽  
Vol 315 (5817) ◽  
pp. 1393-1396 ◽  
Author(s):  
D. C. Pregibon ◽  
M. Toner ◽  
P. S. Doyle
Keyword(s):  
High Throughput ◽  
Encoded Particles

Three-Party Simultaneous Quantum Secure Communication with Unidirectional Qubit Transmission

2015 ◽  
Vol 740 ◽  
pp. 857-860
Author(s):  
Xun Ru Yin
Keyword(s):  
Secure Communication ◽  
Closed Loop ◽  
Communication Protocol ◽  
Quantum Secure Direct Communication ◽  
The Other ◽  
Quantum Channels ◽  
Direct Communication ◽  
Secret Information ◽  
Quantum Secure Communication ◽  
Encoded Particles

A three-party quantum secure direct communication protocol is proposed, in which the qubit transmission forms a closed loop. In this scheme, each party implements the corresponding unitary operations according to his secret bit value over the quantum channels. Then, by performing Bell measurements on the encoded particles, each party can extract the other two parties’ secret information simultaneously. Thus the three parties realize the direct exchange successfully.

scholarly journals Cancer characterization and diagnosis with SERS-encoded particles

2017 ◽  
Vol 8 (1) ◽  
Author(s):  
Luca Guerrini ◽  
Nicolas Pazos-Perez ◽  
Eduardo Garcia-Rico ◽  
Ramon Alvarez-Puebla
Keyword(s):  
Encoded Particles

Generation of multifunctional encoded particles using a tetrapod microneedle injector

2019 ◽  
Vol 74 ◽  
pp. 164-171 ◽  
Author(s):  
Sung-Min Kang ◽  
Muruganantham Rethinasabapathy ◽  
Go-Woon Lee ◽  
Cheol Hwan Kwak ◽  
Bumjun Park ◽  
...  
Keyword(s):  
Encoded Particles

scholarly journals Human Endogenous Retrovirus Family HERV-K(HML-2) RNA Transcripts Are Selectively Packaged into Retroviral Particles Produced by the Human Germ Cell Tumor Line Tera-1 and Originate Mainly from a Provirus on Chromosome 22q11.21

2008 ◽  
Vol 82 (20) ◽  
pp. 10008-10016 ◽  
Author(s):  
Klemens Ruprecht ◽  
Humberto Ferreira ◽  
Aline Flockerzi ◽  
Silke Wahl ◽  
Marlies Sauter ◽  
...  
Keyword(s):  
Germ Cell ◽  
Germ Cell Tumor ◽  
Endogenous Retrovirus ◽  
Cell Tumor ◽  
Human Endogenous Retrovirus ◽  
Tumor Line ◽  
Gag Protein ◽  
Rna Transcripts ◽  
Encoded Particles ◽  
Human Germ Cell Tumor

ABSTRACT The human germ cell tumor line Tera-1 produces retroviral particles which are encoded by the human endogenous retrovirus family HERV-K(HML-2). We show here, by quantitative reverse transcriptase PCR, that HML-2 gag and env RNA transcripts are selectively packaged into Tera-1 retroviral particles, whereas RNAs from cellular housekeeping genes and from other HERV families (HERV-H and HERV-W) are nonselectively copackaged. Assignment of cloned HML-2 gag and env cDNAs from Tera-1 retroviral particles to individual HML-2 loci in the human genome demonstrated that HML-2 RNA transcripts packaged into Tera-1 retroviral particles originate almost exclusively from an HML-2 provirus on chromosome 22q11.21. Based on relative cloning frequencies, this provirus was the most active among a total of eight transcribed HML-2 loci identified in Tera-1 cells. These data suggest that at least one HML-2 element, that is, the HML-2 provirus on 22q11.21, has retained the capacity for packaging RNA into HML-2-encoded retroviral particles. Given its elevated transcriptional activity and the presence of a full-length Gag open reading frame, the 22q11.21 HML-2 provirus may also significantly contribute to Gag protein and thus particle production in Tera-1 cells. Our findings provide important clues to the generation and biological properties of HML-2-encoded particles. In addition, copackaging of non-HML-2 HERV transcripts in HML-2-encoded particles should inform the debate about endogenous retroviral particles putatively encoded by non-HML-2 HERV families that have previously been described for other human diseases, such as multiple sclerosis.

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