US 5591646A
· Hudson et al.
· 1997
[cited by applicant]
US 5605809A
· Komoriya et al.
· 1997
[cited by applicant]
US 5902723A
· Dower et al.
· 1999
[cited by applicant]
US 5914313A
· Bouffard et al.
· 1999
[cited by applicant]
US 6156527A
· Schmidt et al.
· 2000
[cited by applicant]
US 6326136B1
· Lazar et al.
· 2001
[cited by applicant]
US 6902936B2
· Qiu et al.
· 2005
[cited by applicant]
US 7329505B2
· Marme
· 2008
[cited by applicant]
US 7351540B1
· Carr
· 2008
[cited by applicant]
US 7468258B2
· Owen
· 2008
[cited by applicant]
US 7641862B2
· Noetzel et al.
· 2010
[cited by applicant]
US 8268977B2
· Kool et al.
· 2012
[cited by applicant]
US 8569481B2
· Koster et al.
· 2013
[cited by applicant]
US 8609423B2
· Diller et al.
· 2013
[cited by applicant]
US 8778685B2
· Diller et al.
· 2014
[cited by applicant]
US 9011772B2
· Norderhaug et al.
· 2015
[cited by applicant]
US 9175035B2
· Konno et al.
· 2015
[cited by applicant]
US 9188586B2
· Fan et al.
· 2015
[cited by applicant]
US 9435810B2
· Havranek et al.
· 2016
[cited by applicant]
US 9470680B2
· Gonzalez et al.
· 2016
[cited by applicant]
US 9566335B1
· Emili et al.
· 2017
[cited by applicant]
US 9580736B2
· Tan et al.
· 2017
[cited by applicant]
US 9625469B2
· Marcotte et al.
· 2017
[cited by applicant]
US 9689868B2
· Kelts et al.
· 2017
[cited by applicant]
US 9983211B2
· Diller et al.
· 2018
[cited by applicant]
US 11143648B2
· Ashworth-Sharpe et al.
· 2021
[cited by applicant]
US 20020137045A1
· Lukhtanov et al.
· 2002
[cited by applicant]
US 20020168682A1
· Goodlett et al.
· 2002
[cited by applicant]
US 20020182117A1
· Coassin et al.
· 2002
[cited by applicant]
US 20040029181A1
· Ueyama et al.
· 2004
[cited by applicant]
US 20040053356A1
· Duewel et al.
· 2004
[cited by applicant]
US 20040059522A1
· Han et al.
· 2004
[cited by applicant]
US 20050003558A1
· Zuckermann et al.
· 2005
[cited by applicant]
US 20050020810A1
· Ternansky et al.
· 2005
[cited by applicant]
US 20080090238A1
· Yang et al.
· 2008
[cited by applicant]
US 20080206141A1
· Johannesen
· 2008
[cited by applicant]
US 20080242838A1
· Peters et al.
· 2008
[cited by applicant]
US 20100047170A1
· Denmeade et al.
· 2010
[cited by applicant]
US 20100047814A1
· Bruce et al.
· 2010
[cited by applicant]
US 20100233095A1
· Duan et al.
· 2010
[cited by applicant]
US 20100255518A1
· Goix et al.
· 2010
[cited by applicant]
US 20100331199A1
· Stoll et al.
· 2010
[cited by applicant]
US 20110027300A1
· Ugurbil et al.
· 2011
[cited by applicant]
US 20140024124A1
· Shinohara et al.
· 2014
[cited by applicant]
US 20150087526A1
· Hesselberth
· 2015
[cited by applicant]
US 20150185199A1
· Joo
· 2015
[cited by applicant]
US 20160194699A1
· Borodina et al.
· 2016
[cited by applicant]
US 20170212126A1
· Emili et al.
· 2017
[cited by applicant]
US 20170343545A1
· Hadrup et al.
· 2017
[cited by applicant]
US 20180284125A1
· Gordon et al.
· 2018
[cited by applicant]
US 20190085412A1
· Fan et al.
· 2019
[cited by applicant]
US 20200123593A1
· Rothberg et al.
· 2020
[cited by applicant]
US 20200123594A1
· Rothberg et al.
· 2020
[cited by applicant]
US 20200124613A1
· Marcotte et al.
· 2020
[cited by applicant]
US 20200348307A1
· Beierle et al.
· 2020
[cited by applicant]
US 20210010070A1
· Schnall-Levin et al.
· 2021
[cited by applicant]
US 20210215706A1
· Marcotte et al.
· 2021
[cited by applicant]
US 20210215707A1
· Marcotte et al.
· 2021
[cited by applicant]
US 20220163536A1
· Marcotte et al.
· 2022
[cited by applicant]
EP 1163519A1
· 2001
[cited by applicant]
EP 2518514
· 2012
[cited by applicant]
EP 3219712A1
· 2017
[cited by applicant]
EP 3821010A1
· 2021
[cited by applicant]
GB 2610078
· 2023
[cited by applicant]
WO WO9100296
· 1991
[cited by applicant]
WO WO9312230
· 1993
[cited by applicant]
WO WO2007070021
· 2007
[cited by applicant]
WO WO2007104219
· 2007
[cited by applicant]
WO WO2007120805
· 2007
[cited by applicant]
WO WO2008109176
· 2008
[cited by applicant]
WO WO2009158006
· 2009
[cited by applicant]
WO WO2010044892
· 2010
[cited by applicant]
WO WO2010065322
· 2010
[cited by applicant]
WO WO2010065531
· 2010
[cited by applicant]
WO WO2012019765
· 2012
[cited by applicant]
WO WO2012071428
· 2012
[cited by applicant]
WO WO2012083261
· 2012
[cited by applicant]
WO WO2012178023
· 2012
[cited by applicant]
WO WO2013112745
· 2013
[cited by applicant]
WO WO2014031997
· 2014
[cited by applicant]
WO WO2014106957
· 2014
[cited by applicant]
WO WO2014124338
· 2014
[cited by applicant]
WO WO2014210353
· 2014
[cited by applicant]
WO WO2015035108
· 2015
[cited by applicant]
WO WO2015153381A2
· 2015
[cited by applicant]
WO WO2015200893
· 2015
[cited by applicant]
WO WO2016069124
· 2016
[cited by applicant]
WO WO2016114970
· 2016
[cited by applicant]
WO WO2016145416
· 2016
[cited by applicant]
WO WO2016164530
· 2016
[cited by applicant]
WO WO2017063093
· 2017
[cited by applicant]
WO WO2017075265
· 2017
[cited by applicant]
WO WO2017079593
· 2017
[cited by applicant]
WO WO2017192633
· 2017
[cited by applicant]
WO WO2017219027
· 2017
[cited by applicant]
WO WO2018075693
· 2018
[cited by applicant]
WO WO2018119447
· 2018
[cited by applicant]
WO WO2018140966
· 2018
[cited by applicant]
WO WO2019063827
· 2019
[cited by applicant]
WO WO2019089836
· 2019
[cited by applicant]
WO WO2019089846
· 2019
[cited by applicant]
WO WO2019089851
· 2019
[cited by applicant]
WO WO2019125982
· 2019
[cited by applicant]
WO WO2019168164
· 2019
[cited by applicant]
WO WO2019178033
· 2019
[cited by applicant]
WO WO2020014586
· 2020
[cited by applicant]
WO WO2020023488A1
· 2020
[cited by applicant]
WO WO2020037046A1
· 2020
[cited by applicant]
WO WO2020072907
· 2020
[cited by applicant]
WO WO2020102741
· 2020
[cited by applicant]
WO WO2020180335
· 2020
[cited by applicant]
WO WO2020223133
· 2020
[cited by applicant]
WO WO2021168083A1
· 2021
[cited by applicant]
WO WO2021211631A2
· 2021
[cited by applicant]
WO WO2021236716A2
· 2021
[cited by applicant]
WO WO2023091961A2
· 2023
[cited by applicant]
Extended European Search Report issued in European Application No. 19868673.5, dated Dec. 13, 2022.
[cited by applicant]
Inoue, Nozomu et al. “Site-Specific Modification of Proteins through N-Terminal Azide Labeling and a Chelation-Assisted CuAAC Reaction.”
[cited by applicant]
Kim, Hwajeong et al. “Stable protein device platform based on pyridine dicarboxylic acid-bound cubic-nanostructured mesoporous titania films.”
[cited by applicant]
Machine Translation of WO 2019/168164, prepared Dec. 7, 2022.
[cited by applicant]
Solulink: “MagnaLink(TM) 4FB Magnetic Beads”, 2012, XP055940075, Retrieved from the Internet: URL:https://vectorlabs.com/media/folio3/productattachments/M-1004-MagnaLink4FBMagnet icBeads.Fix.pdf [retrieved on Jul. 7, 20…
[cited by applicant]
Sumaru, Kimio et al. “Photoresponsive Aqueous Dissolution of Poly( N-Isopropylacrylamide) Functionalized with o-Nitrobenzaldehyde through Phase Transition.”
[cited by applicant]
“The catalog for Molecular Probes”, downloaded from: https://web.archive.org/web/20101217092018/http://www.mobitec.de/probes/docs/sections/0101.pdf, available 2010.
[cited by applicant]
Aitken, Colin Echeverría, R. Andrew Marshall, and Joseph D. Puglisi. “An oxygen scavenging system for improvement of dye stability in single-molecule fluorescence experiments.”
[cited by applicant]
Alfaro, Javier Antonio, et al. “The emerging landscape of single-molecule protein sequencing technologies.” Nature Methods 18.6 (2021): 604-617.
[cited by applicant]
Altman et al., “Cyanine fluorophore derivatives with enhanced photostability,”
[cited by applicant]
Altman, R. B. et al. (2012) “Enhanced photostability of cyanine fluorophores across the visible spectrum,”
[cited by applicant]
Antos et al., “Site-specific protein labeling via sortase-mediated transpeptidation,”
[cited by applicant]
Armbrecht et al., “Single-cell protein profiling in microchambers with barcoded beads,”
[cited by applicant]
Axelrod, D. (1981) “Cell-substrate contacts illuminated by total internal reflection fluorescence,”
[cited by applicant]
Bailey and Shively, “Carboxy-Terminal Sequencing: Formation and Hydrolysis of C-Terminal Peptidylthiohydantoins,”
[cited by applicant]
Bamberger, Casimir, et al. “Protein footprinting via covalent protein painting reveals structural changes of the proteome in Alzheimer's disease.”
[cited by applicant]
Baslé, E. et al. (2010) “Protein Chemical Modification on Endogenous Amino Acids,”
[cited by applicant]
Bendall et al., “Single-Cell Mass Cytometry of Differential Immune and Drug Responses Across a Human Hematopoietic Continuum,”
[cited by applicant]
Berg et al., “Peptide oligomers for holographic data storage,”
[cited by applicant]
Bethell et al., “Kinetics and Mechanism of the Edman Degradation,”
[cited by applicant]
Bhat et al., “The visible touch: in planta visualization of protein-protein interactions by fluorophore-based methods,”
[cited by applicant]
Biedka, Stephanie, et al. “Reversible Click Chemistry Tag for Universal Proteome Sample Preparation for Top-Down and Bottom-Up Analysis.”
[cited by applicant]
Billingsley et al., “Single-molecule studies of DNA transcription using atomic force microscopy,”
[cited by applicant]
Bloom et al., “Decarboxylative alkylation for site-selective bioconjugation of native proteins via oxidation potentials,”
[cited by applicant]
Bonnet et al., “Amplifying Genetic Logic Gates,”
[cited by applicant]
Borgo et al., “Computer-Aided Design of a Catalyst for Edman Degradation Utilizing Substrate-Assisted Catalysis,”
[cited by applicant]
Bottecchia et al., “Photocatalytic modification of amino acids, peptides, and proteins”,
[cited by applicant]
Bradski et al., “OpenCV: an open-source computer vision library,” Dr. Dobb's Journal of Software Tools, 2000.
[cited by applicant]
Brandt, M. (downloaded Feb. 18, 2016) Quenching processes, https://www.rose-hulman.edu/-brandt/Fluorescence/Quenching_processes.pdf.
[cited by applicant]
Branton et al., “The Potential and Challenges of Nanopore Sequencing,”
[cited by applicant]
Braslavsky, I. et al. (2003) “Sequence information can be obtained from single DNA molecules,”
[cited by applicant]
Brewis et al., “Proteomics technologies for the global identification and quantification of proteins”,
[cited by applicant]
Brosseron et al., “Stepwise isolation of human peripheral erythrocytes, T lymphocytes, and monocytes for blood cell proteomics,”
[cited by applicant]
Cafferty et al., “Storage of information using small organic molecules,”
[cited by applicant]
Cang, H. et al. (2013) “Giant suppression of photobleaching for single molecule detection via the Purcell effect,”
[cited by applicant]
Cannon et al., “A Dual-Mode Single-Molecule Fluorescence Assay for the Detection of Expanded CGG Repeats in Fragile X Syndrome,”
[cited by applicant]
Cao, Ting, et al. “Selective Enrichment and Quantification of N-Terminal Glycine Peptides via Sortase a Mediated Ligation.”
[cited by applicant]
Caron et al., “Analysis of Major Histocompatibility Complex (MHC) Immunopeptidomes Using Mass Spectrometry”,
[cited by applicant]
Chalker, J. M. et al. (2009) “Chemical Modification of Proteins at Cysteine: Opportunities in Chemistry and Biology,”
[cited by applicant]
Chang, “Manual Solid Phase Sequence Analysis of Polypeptides Using 4-N,N-Dimethylaminoazobenzene 4′-Isothiocyanate,”
[cited by applicant]
Chelius, Dirk, and Thomas A. Sbaler. “Capture of peptides with N-terminal serine and threonine: a sequence-specific chemical method for peptide mixture simplification.”
[cited by applicant]
Chen et al., “An efficient and versatile approach for the preparation of a rhodamine B ester bioprobe library,”
[cited by applicant]
Chen et al., “Reactivity of functional groups on the protein surface: development of epoxide probes for protein labeling.”
[cited by applicant]
Chen et al., “Spatially resolved, highly multiplexed RNA profiling in single cells”,
[cited by applicant]
Choi et al., “Core-shell silica nanoparticles as fluorescent labels for nanomedicine,”
[cited by applicant]
Church et al., “Next-Generation Digital Information Storage in DNA.”
[cited by applicant]
Cline, G. W. et al. (1988) “Kinetics and mechanisms of the aminolysis of N-hydroxysuccinimide esters in aqueous bnffers,” Journal of Organic Chemistry 53(15), 3583-3586.
[cited by applicant]
Cockrill, S. L. et al. (2005) “Efficient micro-recovery and guanidination of peptides directly from MALDI target spots,”
[cited by applicant]
Cohen et al., “Red cell life span heterogeneity in hematologically normal people is sufficient to alter HbA1c,”
[cited by applicant]
Colombani, Oliver et al., “Polymerization kinetics: monitoring monomer conversion using an internal standard and the key role of sample to.”
[cited by applicant]
Co-pending U.S. Appl. No. 17/491,485, inventors Marcotte; Edward et al., filed Sep. 30, 2021.
[cited by applicant]
Co-pending U.S. Appl. No. 17/738,281, inventors Marcotte; Edward et al., filed May 6, 2022.
[cited by applicant]
Cordes and Blum, “Opportunities and Challenges in Single-Molecule and Single-Particle Fluorescence Microscopy for Mechanistic Studies of Chemical Reactions,”
[cited by applicant]
Cordes et al., “On the Mechanism of Trolox as Antiblinking and Antibleaching Reagent,”
[cited by applicant]
Croop, Benjamin, Jialei Tang, and Kyu Young Han. “Single-shot, shadowless total internal reflection fluorescence microscopy via annular fiber bundle.”
[cited by applicant]
Cuppoletti et al., “Oligomeric Fluorescent Labels for DNA,”
[cited by applicant]
Czaplyski, W. L. et al. (2014) “Substituent effects on the tum-on kinetics of rhodamine-based fluorescent pH probes,”
[cited by applicant]
Da Costa et al., “How low can you go? A current perspective on low-abundance proteomics,”
[cited by applicant]
D'Amici et al., “Red blood cell storage in SAGM and AS3: a comparison through the membrane two-dimensional electrophoresis proteome,”
[cited by applicant]
Declaration of Dr. Edward Marcotte filed in U.S. Appl. No. 14/128,247, filed Jul. 7, 2016.
[cited by applicant]
Declaration of Dr. Edward Marcotte filed in U.S. Appl. No. 14/128,247, filed Sep. 2, 2016.
[cited by applicant]
Declaration of Dr. Jagannath Swaminathan filed in U.S. Appl. No. 14/128,247, filed Jan. 26, 2016.
[cited by applicant]
Dempsey et al., “Evaluation of Fluorophores for Optimal Performance in Localization-Based Super-Resolution Imaging.”
[cited by applicant]
Dixon, H. B., and R. N. Perham. “Reversible blocking of amino groups with citraconic anhydride.”
[cited by applicant]
Doll, et al. Visualization of Protein-Specific Glycosylation inside Living Cells. Angewandte Chemie International Edition 55.6 (2016): 2262-2266. Supporting Information.
[cited by applicant]
Dong et al., “Label-free quantitation of glycated hemoglobin in single red blood cells by transient absorption microscopy and phasor analysis”,
[cited by applicant]
Donnert et al., “Major signal increase in fluorescence microscopy through dark-state relaxation,”
[cited by applicant]
Doolittle, L. R., et al. “A simple solid-phase amino acid sequencer employing a thioacetylation stepwise degradation procedure.”
[cited by applicant]
Edman, P. (1949) “A method for the determination of amino acid sequence in peptides.”
[cited by applicant]
Edman, P. (1950) “Method for determination of the amino acid sequence in peptides,”
[cited by applicant]
Edman, P. et al. (1967) “A Protein Sequenator,”
[cited by applicant]
Egloff et al., “Engineered peptide barcodes for in-depth analyses of binding protein libraries,”
[cited by applicant]
Eid, J. et al. (2009) “Real-time DNA sequencing from single polymerase molecules,”
[cited by applicant]
Eliason, Robert et al, “Temperature effect on reaction rates.”
[cited by applicant]
Ellson et al., “Graphviz and Dynagraph—Static and Dynamic Graph Drawing Tools”,
[cited by applicant]
EP19834092.9 extended European Search Report dated Mar. 18, 2022.
[cited by applicant]
EP19849103.7 Extended European Search Report dated May 16, 2022.
[cited by applicant]
EP20150854171 European Search Report dated Feb. 12, 2018.
[cited by applicant]
EP20150854171 Extended European Search Report dated Jun. 6, 2018.
[cited by applicant]
EP20180215779 European Search Report dated Jul. 26, 2019.
[cited by applicant]
Fields et al., “The interplay of biology and technology,”
[cited by applicant]
Fina, Nick J., and John O. Edwards. “The alpha effect. A review.”
[cited by applicant]
Fredkin, E. (1960) “Trie memory,”
[cited by applicant]
Frey, B. L. et al. (2013) “Chemical derivatization of peptide carboxyl groups for highly efficient electron transfer dissociation,”
[cited by applicant]
Fukuzaki, Satoshi et al, “Adsorption of protein onto stainles steel surfaces.”
[cited by applicant]
Gajer et al., “A Multi-dimensional Approach to Force-Directed Layouts of Large Graphs,”
[cited by applicant]
Garcia-Parajo, M. F. et al. (2001) “The nature of fluorescence emission in the red fluorescent protein DsRed, revealed by single-molecule detection,”
[cited by applicant]
Garreau et al., “C-Terminal Bioconjugation of Peptides through Photoredox Catalyzed Decarboxylative Alkynylation,”
[cited by applicant]
Gawad et al., “Single-cell genome sequencing: current state of the science,”
[cited by applicant]
Ghaemmaghami et al., “Global analysis of protein expression in yeast,”
[cited by applicant]
Gilmore, Joshua M. et al, “N-terminal protein modification through a biomimetic transamination reaction.”
[cited by applicant]
Gooley, A. A. et al. (1991) “Glycosylation sites identified by detection of glycosylated amino acids released from Edman degradation: The identification of Xaa-Pro-Xaa-Xaa as a motif for Thr-O-glycosylation,”
[cited by applicant]
Gullberg et al., “A sense of closeness: protein detection by proximity ligation”,
[cited by applicant]
Gyarmati et al., “Reversible disulphide formation in polymer networks: A versatile functional group from synthesis to applications”,
[cited by applicant]
Haab, B. B. (2006) “Applications of antibody array platforms,”
[cited by applicant]
Hamada, Yoshio. “A novel N-terminal degradation reaction of peptides via N-amidination.”
[cited by applicant]
Han, K.-K. et al. (1985) “Current developments in stepwise edman degradation of peptides and proteins,”
[cited by applicant]
Hanay, M. S. et al. (2012) “Single-protein nanomechanical mass spectrometry in real time,”
[cited by applicant]
Haralambidis et al., “The preparation of polyamide-oligonucleotide probes containing multiple non-radioactive labels,”
[cited by applicant]
Harris, T. D. et al. (2008) “Single-Molecule DNA Sequencing of a Viral Genome,”
[cited by applicant]
Hartmann et al., “A universal live cell barcoding-platform for multiplexed human single cell analysis,”
[cited by applicant]
Havugimana et al., “A Census of Human Soluble Protein Complexes,”
[cited by applicant]
Herbrink, P. ( 197 5) “Solid phase Edman degradation. High yield attachment of tryptic protein fragments to aminated supports,”
[cited by applicant]
Hernandez, Erik T., et al. “Solution-phase and solid-phase sequential, selective. Modification of side chains in KDYWEC and KDYWE as models for usage in single-molecule protein sequencing.”
[cited by applicant]
Higgins et al., “Kinetic analysis of the nonenzymatic glycosylation of hemoglobin,”
[cited by applicant]
Hoebe, R. A. et al. (2007) “Controlled light-exposure microscopy reduces photobleaching and phototoxicity in fluorescence live-cell imaging,”
[cited by applicant]
Hong, Jessica M., et al. “ProtSeq: Toward bigh-throughput, single-molecule protein sequencing via amino acid conversion into DNA barcodes.”
[cited by applicant]
Horton, H. R. et al. (1965) “A Highly Reactive Colored Reagent with Selectivity for the Tryptophan Residue in Proteins. 2-Hydroxy-5-nitrobenzyl Bromidel,”
[cited by applicant]
Howard, Cecil J., et al. “Solid-phase peptide capture and release for bulk and single-molecule proteomics.”
[cited by applicant]
Huang et al., “Super resolution fluorescence microscopy,”
[cited by applicant]
Huang et al., “Three-Dimensional Super-Resolution Imaging by Stochastic Optical Reconstruction Microscopy,”
[cited by applicant]
Huang, Xiaodong, and Vishva M. Dixit. “Drugging the undruggables: exploring the ubiquitin system for drug development.”
[cited by applicant]
Hughes et al., “Single-cell western blotting,”
[cited by applicant]
Imakyure et al., “A Fluorogenic Reagent for Amino Acids in Liquid Chromatography, 4-(2-Cyanoisoindolyl)Phenylisothiocyanate,”
[cited by applicant]
Inglis, “Chemical Procedures for C-Terminal Sequencing of Peptides and Proteins.”
[cited by applicant]
Ingolia, N. T. et al. (2009) “Genome-Wide Analysis in Vivo of Translation with Nucleotide Resolution Using Ribosome Profiling,”
[cited by applicant]
Ireland et al., “Double Coupling Edman Chemistry for High-Sensitivity Automated Protein Sequencing,”
[cited by applicant]
Isidro-Llobet, A. et al. (2009) “Amino Acid-Protecting Groups,”
[cited by applicant]
Jain et al., “Stoichiometry and assembly of mTOR complexes revealed by single-molecule pulldown,”
[cited by applicant]
Jameson, David M. and Ross, Justin A, “Fluorescence polarization/anisotropy in diagnostics and imaging.”
[cited by applicant]
Javitt, Aaron, et al. “The proteasome regulator PSME4 drives immune evasion and abrogates anti-tumor immunity in NSCLC.”
[cited by applicant]
Jin, S.-W. et al. (1989) “Study on New Edman-type Reagents,” in Methods in Protein Sequence Analysis (Wittmann-Liebold, B., Ed.), pp. 34-41, Springer Berlin Heidelberg, Berlin, Heidelberg.
[cited by applicant]
Johnson et al., “Reversible macrocyclization of peptides with a conjugate acceptor,”
[cited by applicant]
Joo, C. et al. (2008) “Advances in single-molecule fluorescence methods for molecular biology,”
[cited by applicant]
Julka, S. et al. (2004) “Quantification in Proteomics through Stable Isotope Coding: A Review,”
[cited by applicant]
Jungmann et al., “Quantitative Super-Resolution Imaging with QPAINT,”
[cited by applicant]
Katritzky et al., “Fluorescent labeling of peptides on solid phase,”
[cited by applicant]
Kelly, K. A. et al. (2008) “Targeted Nanoparticles for Imaging Incipient Pancreatic Ductal Adenocarcinoma,” PLoS Medicine 5(4), e85.
[cited by applicant]
Keough, T. et al. (2000) “Derivatization procedures to facilitate de novo sequencing of Lysine-terminated tryptic peptides using postsource decay matrix-assisted laser desorption/ionization mass spectrometry,”
[cited by applicant]
Kim et al., “C-terminal de novo sequencing of peptides using oxazolone-based derivatization with bromine signature”,
[cited by applicant]
Kinraide, “Use of a Gouy-Chapman-Stern Model for Membrane-Surface Electrical Potential to Interpret Some Features of Mineral Rhizotoxicity,”
[cited by applicant]
Ko, B. J. et al. (2012) “Enhanced electron transfer dissociation of peptides modified at C-terminus with fixed charges,”
[cited by applicant]
Koide, Y. et al. (2012) “Development of NIR Fluorescent Dyes Based on Si-rhodamine for in Vivo Imaging,”
[cited by applicant]
Konry et al., “Droplet-based microfluidic platforms for single T cell secretion analysis of IL-10 cytokine,”
[cited by applicant]
Koos et al., “Analysis of protein interactions in situ by proximity ligation assays,”
[cited by applicant]
Kovalova et al., “Stepwise triple-click functionalization of synthetic peptides,”
[cited by applicant]
Krusemark, C. J. et al. (2011) “Complete chemical modification of amine and acid functional groups of peptides and small proteins,”
[cited by applicant]
Kuyama, H. et al. (2003) “An approach to quantitative proteome analysis by labeling tryptophan residues,”
[cited by applicant]
Lakowicz, ed., “Mechanisms and Dynamics of Fluorescence Quenching,” In:
[cited by applicant]
Lamesch et al., “hORFeome v3.1: a resource of human open reading frames representing over 10,000 human genes,”
[cited by applicant]
Laursen, R. A. (1971) “Solid-Phase Edman Degradation,”
[cited by applicant]
Lee et al., “Evidence of preserved collagen in an Early Jurassic sauropodomorph dinosaur revealed by synchrotron FTIR microspectroscopy,”
[cited by applicant]
Leigh-Smith et al., “Blood boosting,”
[cited by applicant]
Li et al., “N-terminal α-amino group modification of antibodies using a site-selective click chemistry method,”
[cited by applicant]
Li, Sujun, Alex DeCourcy, and Haixu Tang. “Constrained De Novo sequencing of neo-epitope peptides using tandem mass spectrometry.”
[cited by applicant]
Li, Z.-S. et al. (2013) “Synthesis and biological evaluation of nonsymmetrical aromatic disulfides as novel inhibitors of acetohydroxyacid synthase,”
[cited by applicant]
Liu et al., “On the dependency of cellular protein levels on mRNA abundance,”
[cited by applicant]
Lo et al., “Quantification of protein levels in single living cells,”
[cited by applicant]
Lotze et al., “Peptide-tags for site-specific protein labelling in vitro and in vivo”,
[cited by applicant]
Luchowski et al., “Single molecule studies of multiple-fluorophore labeled antibodies. Effect of homo-FRET on the number of photons available before photobleaching,”
[cited by applicant]
Lukinavious et al., “A near-infrared fluorophore for live-cell super-resolution microscopy of cellular proteins,”
[cited by applicant]
Lyon et al., “Self-hydrolyzing maleimides improve the stability and pharmacological properties of antibody-drug conjugates,”
[cited by applicant]
Macbeath, G. et al. (1999) “Printing Small Molecules as Microarrays and Detecting Protein-Ligand Interactions en Masse,”
[cited by applicant]
MacDonald et al., “One-Step Site-Specific Modification of Native Proteins with 2-Pyridinecarboxyaldehydes,”
[cited by applicant]
Maiti et al., “Bifunctional aryloxyphosphoramidate prodrugs of 2′-C-Me-uridine: synthesis and anti-HCV activity”,
[cited by applicant]
Mallam et al., “Systematic discovery of endogenous human ribonucleoprotein complexes,”
[cited by applicant]
Martins, Joana N., João Carlos Lima, and Nuno Basilio. “Selective recognition of amino acids and peptides by small supramolecular receptors.”
[cited by applicant]
Martos-Maldonado, Manuel C., et al. “Selective N-terminal acylation of peptides and proteins with a Gly-His tag sequence.”
[cited by applicant]
Matsunaga et al., “Proton: A Major Factor for the Racemization and the Dehydration at the Cyclization/Cleavage Stage in the Edman Sequencing Method,”
[cited by applicant]
Mazutis et al., “Single-cell analysis and sorting using droplet-based microfluidics,”
[cited by applicant]
McAlpine, S. R. et al. (1999) “Visualizing Functional Group Distribution in Solid-Support Beads by Using Optical Analysis,”
[cited by applicant]
Millington, C. R. et al. (1998) “Aryl hydrazides as linkers for solid phase synthesis which are cleavable under mild oxidative conditions,”
[cited by applicant]
Miyamoto, Kana, et al. “Peptide barcoding for establishment of new types of genotype-phenotype linkages.”
[cited by applicant]
Miyashita et al., “Attomole Level Protein Sequencing by Edman Degradation Coupled with Accelerator Mass Spectrometry,”
[cited by applicant]
Moffett, J. R. et al. (2003) “Tryptophan and the immune response,”
[cited by applicant]
Mohanty et al., “Advancing cell biology and functional genomics in maize using fluorescent protein-tagged lines,”
[cited by applicant]
Momaya et al., “Performance-Enhancing Substances in Sports: A Review of the Literature,”
[cited by applicant]
Monfort et al., “Plasticizers excreted in urine: indication of autologous blood transfusion in sports,”
[cited by applicant]
Muramoto et al., “The Application of Fluorescein Isothiocyanate and High-Performance Liquid Chromatography for the Microsequencing of Proteins and Peptides,”
[cited by applicant]
Murata, Hironobu, et al. “Solid-phase synthesis of protein-polymers on reversible immobilization supports.”
[cited by applicant]
Nagaraj, N. et al. (2011) “Deep proteome and transcriptome mapping of a human cancer cell line,”
[cited by applicant]
Ng, Cheuk Chi A., et al. “Data storage using peptide sequences.”
[cited by applicant]
Nguyen, Giang KT, et al. “Butelase-mediated cyclization and ligation of peptides and proteins.”
[cited by applicant]
Niall, H. D. (1973) “[36] Automated edman degradation: The protein sequenator,”
[cited by applicant]
Nikon. (2010) Nikon microscopes educational literature, https://www.microscopyu.coru/references/photobleaching.html.
[cited by applicant]
Nivala, J. et al. (2013) “Unfoldase-mediated protein translocation through an a-hemolysin nanopore,”
[cited by applicant]
Nuijens et al., “Improved solid phase synthesis of peptide carboxyamidomethyl (Cam) esters for enzymatic segment condensation”,
[cited by applicant]
Office Communication issued in GB1322371.4, dated Nov. 26, 2018.
[cited by applicant]
Office Communication issued in GB1322371.4, dated Jul. 29, 2019.
[cited by applicant]
Office Communication issued in GB1322371.4, dated Nov. 8, 2019.
[cited by applicant]
Office Communication issued in GB1912227.4, dated Nov. 11, 2019.
[cited by applicant]
Office Communication issued in U.S. Appl. No. 15/461,034, dated Jun. 29, 2018.
[cited by applicant]
Office Communication issued in U.S. Appl. No. 15/461,034, dated Nov. 20, 2018.
[cited by applicant]
Office Communication issued in U.S. Appl. No. 15/510,962, dated Dec. 6, 2018.
[cited by applicant]
Office Communication issued in U.S. Appl. No. 15/510,962, dated May 3, 2019.
[cited by applicant]
Office Communication issued in U.S. Appl. No. 15/510,962, dated Sep. 11, 2019.
[cited by applicant]
Oquare, “Design and Synthesis of Peptide Nucleic Acid (PNA) Agents”, Dissertation, Washington University, 2007.
[cited by applicant]
Ortiz et al., “Design of multivalent fluorescent dendritic probes for site-specific labeling of biomolecules,”
[cited by applicant]
PCT International Search Report and Written Opinion issued in PCT/US2022/017642 on Jul. 19, 2022.
[cited by applicant]
PCT International Search Report and Written Opinion issued in PCT/US2022/031022 on Aug. 19, 2022.
[cited by applicant]
PCT International Search Report of International Application No. PCT/US2012/043769 dated Oct. 4, 2012.
[cited by applicant]
PCT/US19/46507 International Search Report dated Dec. 10, 2019.
[cited by applicant]
PCT/US2015/050099 International Search Report and Written Opinion dated Apr. 11, 2016.
[cited by applicant]
PCT/US2019/041562 International Search Report and Written Opinion dated Oct. 11, 2019.
[cited by applicant]
PCT/US2019/042998 International Search Report dated Oct. 31, 2019.
[cited by applicant]
PCT/US2019/054702 International Search Report and Written Opinion dated Feb. 6, 2020.
[cited by applicant]
PCT/US2021/018535 International Search Report and Written Opinion dated Jul. 1, 2021.
[cited by applicant]
PCT/US2021/027155 International Search Report and Written Opinion dated Oct. 14, 2021.
[cited by applicant]
PCT/US2021/033077 International Search Report and Written Opinion dated May 18, 2022.
[cited by applicant]
Peplow et al., “Molecular data-storage system encodes information with peptides,”
[cited by applicant]
Perron, Y. G. et al. (1961) “Derivatives of 6-Aminopenicillanic Acid. II. Reactions with Isocyanates, Isothiocyanates, and Cyclic Anhydrides,” Journal of Organic Chemistry 26(9), 3365-3367.
[cited by applicant]
Peters, Eric C., et al. “A novel multifunctional labeling reagent for enhanced protein characterization with mass spectrometry.”
[cited by applicant]
Pickens et al., “Practical Considerations, Challenges, and Limitations of Bioconjugation via Azide-Alkyne Cycloaddition,”
[cited by applicant]
Pieroni et al. (1975) “Reaction of diazonium salt with tyrosine residues in polypeptides,”
[cited by applicant]
Powell and Tempst, “Microflow-Based Automated Chemistries: Application to Protein Sequencing,”
[cited by applicant]
Previero, A. et al. (1973) “Solid phase sequential analysis: Specific linking of acidic peptides by their carboxyl ends to insoluble resins,”
[cited by applicant]
Prosenz et al., “Glycated hemoglobin concentrations of red blood cells minimally increase during storage under standard blood banking conditions,”
[cited by applicant]
Prudent et al., “Proteomics of stored red blood cell membrane and storage-induced microvesicles reveals the association of flotillin-2 with band 3 complexes,”
[cited by applicant]
Purushottam, Landa, et al. “Single-site glycine-specific labeling of proteins.”
[cited by applicant]
Romond, E. H. et al. (2005) “Trastuzumab plus Adjuvant Chemotherapy for Operable HER2-Positive Breast Cancer,”
[cited by applicant]
Roper Scientific. (2015) Datasheet for 1-pentarnax camera, http://www.spectracore.coru/cameras/pdf/ipgeniii.pdf.
[cited by applicant]
Rosenbaum, C. et al. (2001) “Solid phase synthesis of cyclic peptides by oxidative cyclative cleavage of an aryl hydrazide linker—synthesis of stylostatin 1,”
[cited by applicant]
Rothbauer et al., “Speed up to find the right ones: rapid discovery of functional nanobodies,”
[cited by applicant]
Rutten et al., “Encoding information into polymers,”
[cited by applicant]
Ryazantsev et al., “Two-dye and one-or two-quencher DNA probes for real-time PCR assay: synthesis and comparison with a TaqMan™ probe,”
[cited by applicant]
Salehi-Reyhani et al., “A first step towards practical single cell proteomics: a microfluidic antibody capture chip with TIRF detection,”
[cited by applicant]
Saul et al., “Development of a full-length human protein production pipeline,”
[cited by applicant]
Sawyers, C. L. (2008) “The cancer biomarker problem,”
[cited by applicant]
Scangarello, F. A. (2012) Application of mulivalent displays on metalloprotease-dependent cleavage of semaphorin 4d in synapse development, in Department of Biochemistry, Brandeis University.
[cited by applicant]
Schaus et al., “A DNA nanoscope via auto-cycling proximity recording,”
[cited by applicant]
Schmidt et al., “Omniligase-1: a powerful tool for peptide head-to-tail cyclization,”
[cited by applicant]
Scoffone, E. et al. (1966) “Selective modification of the tryptophan residue in peptides and proteins using sulfenyl halides,”
[cited by applicant]
Scoffone, E. et al. (1968) “Sulfenyl halides as modifying reagents for polypeptides and proteins. I. Modification of tryptophan residues,”
[cited by applicant]
Segura et al., “Detection methods for autologous blood doping,”
[cited by applicant]
Shi et al., “Single-cell proteomic chip for profiling intracellular signaling pathways in single tumor cells,”
[cited by applicant]
Sigal et al., Mapping Synaptic Input Fields of Neurons with Super-Resolution Imaging,
[cited by applicant]
Song, L. et al. (1995) “Photobleaching kinetics of fluorescein in quantitative fluorescence microscopy,”
[cited by applicant]
Stevanovic et al., “Multiple Sequence Analysis: Pool Sequencing of Systemic and Natural Peptide Libraries”,
[cited by applicant]
Supplemental Search Report issued in European Application No. 15854171.4, dated Feb. 12, 2018.
[cited by applicant]
Swaminathan, Jagannath, Alexander A. Boulgakov, and Edward M. Marcotte. “A theoretical justification for single molecule peptide sequencing.”
[cited by applicant]
Swaminathan, Jagannath, et al. “Highly parallel single-molecule identification of proteins in zeptomole-scale mixtures.”
[cited by applicant]
Swoboda et al., “Enzymatic oxygen scavenging for photostability without pH drop in single-molecule experiments,”
[cited by applicant]
Szymczak et al., “Peptide arrays: development and application,”
[cited by applicant]
Tang et al., “Development and applications of single-cell transcriptome analysis,”
[cited by applicant]
Taylor, “Aminopeptidases: Structure and Function.”
[cited by applicant]
Tessier et al., “Doubly Orthogonal” Labeling of Peptides and Proteins,
[cited by applicant]
Thakur, S. S. et al. (2011) “Deep and Highly Sensitive Proteome Coverage by LC-MS/MS Without Prefractionation,”
[cited by applicant]
The Scientist Solution Forum (2009), http://www.scientistsolutions.coru/tl1153-keratin+contamination.html.
[cited by applicant]
The University of Cambridge. (2009) Michaelis-Menten equation, http://wwwjmg.ch.cam.ac.uk/tools/magnus/michmenten.html.
[cited by applicant]
Thermo Scientific. (2005) “Thermo Scientific Pierce Cross-Linking Reagents Technical Handbook,” 1-48.
[cited by applicant]
Thoma et al., “The ABRF Edman Sequencing Research Group 2008 Study: Investigation into Homopolymeric Amino Acid N-Terminal Sequence Tags and Their Effects on Automated Edman Degradation.”
[cited by applicant]
Tillberg et al., “Protein-retention expansion microscopy of cells and tissues labeled using standard fluorescent proteins and antibodies,”
[cited by applicant]
Tokeshi, Manabu et al., “Single and countable moleucle detection of non-fluorescent molecules in liquid phase.”
[cited by applicant]
Toseland, Christopher P. “Fluorescent labeling and modification of proteins.”
[cited by applicant]
Tsui, Suet Man, et al. “Single red blood cell analysis reveals elevated hemoglobin in poikilocytes.”
[cited by applicant]
Tulla-Puche, J. et al. (2008) “The (classic concept of) solid support,” in The power of functional resins in organic synthesis (Tulla-Puche, J., et al., Eds.), pp. 3-14, Wiley, Weinheim.
[cited by applicant]