scispace - formally typeset
Search or ask a question
Institution

Agilent Technologies

CompanySanta Clara, California, United States
About: Agilent Technologies is a company organization based out in Santa Clara, California, United States. It is known for research contribution in the topics: Signal & Mass spectrometry. The organization has 7398 authors who have published 11518 publications receiving 262410 citations. The organization is also known as: Agilent Technologies, Inc..


Papers
More filters
Journal ArticleDOI
TL;DR: In this paper, the authors developed principle design procedures for a single-layer coaxially fed rectangular microstrip patch antenna through examination of the structure's multiple resonant frequencies as well as the radiation and impedance properties of different antenna geometries.
Abstract: A wide operating bandwidth for a single-layer coaxially fed rectangular microstrip patch antenna can be obtained by cutting a U-shaped slot on the patch. This antenna structure has recently been found experimentally to provide impedance bandwidths of 10%-40%, even with nonair substrates. However, design rules for this antenna have not yet been presented. This paper develops principle design procedures through examination of the structure's multiple resonant frequencies as well as the radiation and impedance properties of different antenna geometries. The approximate design rules are derived by analysis of former experiments, method of moments (MoM) simulations, and measurement results. Simulations and measurements of several antennas designed using these new rules are presented and directions for further study are discussed.

328 citations

Journal ArticleDOI
Alexander W. Bell1, Eric W. Deutsch2, Catherine E. Au1, Robert E. Kearney1, Ron Beavis3, Salvatore Sechi4, Tommy Nilsson1, John J.M. Bergeron1, Thomas A. Beardslee, Thomas Chappell, Gavin Meredith5, Peter J. Sheffield6, Phillip Gray, Mahbod Hajivandi5, Marshall Pope5, Paul F. Predki5, Majlinda Kullolli7, Marina Hincapie7, William S. Hancock7, Wei Jia, Lina Song, Lei Li, Junying Wei, Bing Yang, Jinglan Wang, Wantao Ying, Yangjun Zhang, Yun Cai, Xiaohong Qian, Fuchu He, Helmut E. Meyer8, Christian Stephan8, Martin Eisenacher8, Katrin Marcus8, Elmar Langenfeld8, Caroline May8, Steve A. Carr9, Rushdy Ahmad9, Wenhong Zhu10, Jeffrey W. Smith10, Samir M. Hanash, Jason J. Struthers11, Hong Wang11, Qing Zhang11, Yanming An12, Radoslav Goldman12, Elisabet Carlsohn13, Sjoerd van der Post13, Kenneth E. Hung14, David A. Sarracino15, Kenneth C. Parker14, Bryan Krastins15, Raju Kucherlapati14, Sylvie Bourassa16, Guy G. Poirier16, Eugene A. Kapp17, Heather Patsiouras17, Robert L. Moritz17, Richard J. Simpson17, Benoit Houle, Sylvie Laboissiere1, Pavel Metalnikov, Vivian Nguyen18, Tony Pawson18, Catherine C. L. Wong19, Daniel Cociorva19, John R. Yates19, Michael J. Ellison20, Ana Lopez-Campistrous20, P. D. Semchuk20, Yueju Wang21, Peipei Ping21, Giuliano Elia22, Michael J. Dunn22, Kieran Wynne22, Angela K. Walker23, John R. Strahler23, Philip C. Andrews23, Brian L. Hood24, William L. Bigbee24, Thomas P. Conrads24, Derek Smith25, Christoph H. Borchers25, Gilles A. Lajoie26, Sean C. Bendall26, Kaye D. Speicher27, David W. Speicher27, Masanori Fujimoto28, Kazuyuki Nakamura28, Young Ki Paik, Sang Yun Cho29, Min-Seok Kwon29, Hyoung Joo Lee29, Seul Ki Jeong29, An Sung Chung29, Christine A. Miller30, Rudolf Grimm30, Katy Williams31, Craig A. Dorschel32, Jayson A. Falkner23, Lennart Martens, Juan Antonio Vizcaíno 
TL;DR: Central analysis determined missed identifications, environmental contamination, database matching and curation of protein identifications as sources of problems in liquid chromatography–mass spectrometry–based proteomics.
Abstract: We performed a test sample study to try to identify errors leading to irreproducibility, including incompleteness of peptide sampling, in liquid chromatography-mass spectrometry-based proteomics. We distributed an equimolar test sample, comprising 20 highly purified recombinant human proteins, to 27 laboratories. Each protein contained one or more unique tryptic peptides of 1,250 Da to test for ion selection and sampling in the mass spectrometer. Of the 27 labs, members of only 7 labs initially reported all 20 proteins correctly, and members of only 1 lab reported all tryptic peptides of 1,250 Da. Centralized analysis of the raw data, however, revealed that all 20 proteins and most of the 1,250 Da peptides had been detected in all 27 labs. Our centralized analysis determined missed identifications (false negatives), environmental contamination, database matching and curation of protein identifications as sources of problems. Improved search engines and databases are needed for mass spectrometry-based proteomics.

324 citations

Patent
14 Aug 1996
TL;DR: In this article, a scanning device and method for forming a scanned electronic image include using navigation information that is acquired along with image data, and then rectifying the image data based upon the navigation and image information.
Abstract: A scanning device and method for forming a scanned electronic image include using navigation information that is acquired along with image data, and then rectifying the image data based upon the navigation and image information. The navigation information is obtained in frames. The differences between consecutive frames are detected and accumulated, and this accumulated displacement value is representative of a position of the scanning device relative to a reference. The image data is then positioned-tagged using the position data obtained from the accumulated displacement value. To avoid the accumulation of errors, the accumulated displacement value obtained from consecutive frames is updated by comparing a current frame with a much earlier frame stored in memory and using the resulting difference as the displacement from the earlier frame. These larger displacement steps are then accumulated to determine the relative position of the scanning device.

324 citations

Journal ArticleDOI
TL;DR: This work presents the synthesis of a shape-persistent cage compound by the reversible formation of 24 boronic ester units of 12 triptycene tetraol molecules and 8 triboronic acid molecules, which is a mesoporous material with a very high specific surface area.
Abstract: Recently, porous organic cage crystals have become a real alternative to extended framework materials with high specific surface areas in the desolvated state. Although major progress in this area has been made, the resulting porous compounds are restricted to the microporous regime, owing to the relatively small molecular sizes of the cages, or the collapse of larger structures upon desolvation. Herein, we present the synthesis of a shape-persistent cage compound by the reversible formation of 24 boronic ester units of 12 triptycene tetraol molecules and 8 triboronic acid molecules. The cage compound bears a cavity of a minimum inner diameter of 2.6 nm and a maximum inner diameter of 3.1 nm, as determined by single-crystal X-ray analysis. The porous molecular crystals could be activated for gas sorption by removing enclathrated solvent molecules, resulting in a mesoporous material with a very high specific surface area of 3758 m2 g−1 and a pore diameter of 2.3 nm, as measured by nitrogen gas sorption.

322 citations

Journal ArticleDOI
01 Jan 2007-RNA
TL;DR: A sensitive, accurate, and multiplexed microRNA (miRNA) profiling assay that is based on a highly efficient labeling method and novel microarray probe design that allows rapid design and validation of probes for simultaneous quantitative measurements of all human miRNA sequences in the public databases and to new mi RNA sequences as they are reported.
Abstract: We have developed a sensitive, accurate, and multiplexed microRNA (miRNA) profiling assay that is based on a highly efficient labeling method and novel microarray probe design. The probes provide both sequence and size discrimination, yielding in most cases highly specific detection of closely related mature miRNAs. Using a simple, single-vial experimental protocol, 120 ng of total RNA is directly labeled using Cy3 or Cy5, without fractionation or amplification, to produce precise and accurate measurements that span a linear dynamic range from 0.2 amol to 2 fmol of input miRNA. The results can provide quantitative estimates of the miRNA content for the tissues studied. The assay is also suitable for use with formalin-fixed paraffin-embedded clinical samples. Our method allows rapid design and validation of probes for simultaneous quantitative measurements of all human miRNA sequences in the public databases and to new miRNA sequences as they are reported.

321 citations


Authors

Showing all 7402 results

NameH-indexPapersCitations
Hongjie Dai197570182579
Zhuang Liu14953587662
Jie Liu131153168891
Thomas Quertermous10340552437
John E. Bowers102176749290
Roy G. Gordon8944931058
Masaru Tomita7667740415
Stuart Lindsay7434722224
Ron Shamir7431923670
W. Richard McCombie7114464155
Tomoyoshi Soga7139221209
Michael R. Krames6532118448
Shabaz Mohammed6418817254
Geert Leus6260919492
Giuseppe Gigli6154115159
Network Information
Related Institutions (5)
Technical University of Denmark
66.3K papers, 2.4M citations

80% related

École Polytechnique Fédérale de Lausanne
98.2K papers, 4.3M citations

80% related

Katholieke Universiteit Leuven
176.5K papers, 6.2M citations

80% related

Ghent University
111K papers, 3.7M citations

80% related

Purdue University
163.5K papers, 5.7M citations

80% related

Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20231
20228
2021142
2020157
2019168
2018164