D. Kozak, A. Chen, M. Trau, Profiling Protein-Surface Interactions of Multicomponent Suspensions via Flow Cytometry, Langmuir 24, 1204 (2008). Syeda Rubaiya Nasrin, Tsukasa Ishihara, Arif Md. Le Marois, K. Suhling, D. Richards, A. Zayats. Soc. The fluorescence is excited most efficiently in the range 610 – 645 nm. ✓ Increasing and decreasing the website fonts 550/30 TagYFP: 508: 524: 488, 514, 532: . Xie, J. Guillot, S. Yucel, P. Li, J. Galván, E. Karamitopoulou, I. Zlobec, D. Ataca, F. Gallean, P. Zhang, J. Rodriguez-Calero, M. Rubin, M. Tichet, K. Homicsko, D. Hanahan, Aberrant hyperexpression of the RNA binding protein FMRP in tumors mediates immune evasion, Science 378 (2022). B. Hellenkamp, S. Schmid, O. Doroshenko, O. Opanasyuk, R. Kühnemuth, S. Rezaei Adariani, B. Ambrose, M. Aznauryan, A. Barth, V. Birkedal, M. Bowen, H. Chen, T. Cordes, T. Eilert, C. Fijen, C. Gebhardt, M. Götz, G. Gouridis, E. Gratton, T. Ha, P. Hao, C. Hanke, A. Hartmann, J. Hendrix, L. Hildebrandt, V. Hirschfeld, J. Hohlbein, B. Hua, C. Hübner, E. Kallis, A. Kapanidis, J.-Y. M. Pazos, K. Peters, M. Casanova, P. Palacios, M. VanNieuwenhze, E. Breukink, M. Vicente, W. Vollmer. 4, 1000134 (2013). S. Simoncelli, W. de Alwis, C. Fasciani, C. Boddy, P. Aramendía, E. Alarcon, J. Scaiano, Thermoplasmonic ssDNA Dynamic Release from Gold Nanoparticles Examined with Advanced Fluorescence Microscopy, The Journal of Physical Chemistry Letters 6, 1499 (2015). 83, 1307 (2011). A. T` GDbqb~Jh!7}IXc-tOa^ To detect far-red fluorescence in cells labeled with the Alexa Fluor 647 or Cy5 A set of polymer particles stained with at least two fluorescent dyes is presented. She, R. Tornay, E. Leimgruber, D. Bernasconi, L. Lagopoulos, P. Renaud, N. Demierre, P. van den Bogaard, Rapid, sensitive and real-time multiplexing platform for the analysis of protein and nucleic-acid biomarkers, Analytical Chemistry 87, 1582 (2015). 2 Images : +351 30 8808 050 Fax : +351 30 8808 052 info@quimigen.pt www.quimigen.pt Expression of TRPV4 in rat DRG primary culture - Immunocytochemical staining of paraformaldehyde-fixed and permeabilized rat dorsal root ganglion (DRG) primary culture.A D. Staining usingAnti-TRPV4Antibody (#ACC-034) (1:500) followed by goat anti-rabbit-AlexaFluor-555 secondary antibody.B E. Nuclear staining of cells using the cell-permeable dye Hoechst 33342.C. ✓ Customized protein/peptide labeling, Subscribe Mark, U. Khadilka, F. Mohring, R. Moon, R. Ramasamy, A dual colour fluorescence in situ hybridization (FISH) assay for identifying the zoonotic malaria parasite Plasmodium knowlesi with a potential application for the specific diagnosis of knowlesi malaria in peripheral-level laboratories of Southeast Asia, Parasites & vectors 10, 342 (2017). Clicking on the menu opens accessibility buttons. Y. Cheng, T. Stakenborg et al., Fluorescence Near Gold Nanoparticles for DNA Sensing, Anal. It can be excited using a 561 nm laser paired with a 586/15 nm bandpass filter, a configuration that can be found, for example, in the BD FACSCelesta™. Commun. Super Bright Polymer Dyes are sold under license from Becton, Dickinson and Company. Herten, G. Nette, G. Schenk, M. Seefeld, Is CuII Coordinated to Patellamides inside Prochloron Cells?, Chemistry - A European Journal (2017). Luke Summer House Ex Girlfriend, High quality Stains, Dyes and Fluorescent Probes with Emission 570-590 nm in the Yellow range are available for use in various immunoassays including Flow Cytometry, Immunofluorescense, Immunohistochemistry, and other applications. Bode Plot Solved Examples In Control System Pdf, 0000002715 00000 n Human coupling factor 6 was labeled by ATTO 550, a new fluorescent dye for protein. E. Ronzitti, B. Harke, A. Diaspro, Frequency dependent detection in a STED microscope using modulated excitation light, Optics Express 21, 201 (2013). Bioelectr. FLOW CYTOMETRY HANDBOOK - Cedarlane 0000186798 00000 n Y. Jiang, A. Matevossian, H.-S. Huang, J. Straubhaar, Sch. Fan. J. Shah, H. Weltman, P. Narciso, C. Murphy, A. Poruri, S. Baliga, L. Sharon, M. York, G. Cunningham, S. Miller, L. Caviedes, R. Gilman, E. Desmond, R. Ramasamy, Dual color fluorescence in situ hybridization (FISH) assays for detecting Mycobacterium tuberculosis and Mycobacterium avium complexes and related pathogens in cultures, PLOS ONE 12, e0174989 (2017). C 114, 4345 (2010). Designed to be affordable and expandable, the BD LSRFortessa System has the flexibility to support the expanding needs of multicolor flow cytometry assays. R. H. Meltzer, J. R. Krogmeier et al., A lab-on-chip biothreat detection using single-molecule DNA mapping, Lab Chip 11, 863 (2011). The dye is moderately hydrophilic. This label is analogous to the well known dye fluorescein isothiocyanate (FITC) and can be used with filters typically used to detect FITC. Mark, U. Khadilka, F. Mohring, R. Moon, R. Ramasamy. View theBD LSRFortessa System brochure. Intracellular flow cytometry Grning et al., A molecular toolkit for population genetic investigations of the ash dieback pathogen Hymenoscyphus pseudoalbidus, For. Flow Cytometry Staining Buffer (Catalog # FC001) or an equivalent solution containing BSA and sodium azide 7-AAD Staining Solution: 1 mg/mL 7-AAD in PBS (store at 2-8 C in the dark) Materials Required FACS Tubes (5 mL round-bottom polystyrene tubes) Pipette Tips and Pipettes Centrifuge Vortex Procedure The light produced by lasers in a flow cytometer is scattered by cells in the sample, measured by detectors, and then translated to signals that can be analyzed and measured. ATTO-550 (554/576) and ATTO-620 channel. This flexibility in laser wavelengths allows assay design to be optimized using the latest fluorescent dyes and substrates. S. Mukherjee, J.-M. Knop, S. Möbitz, R. Winter, Alteration of the Conformational Dynamics of a DNA Hairpin by α-Synuclein in the Presence of Aqueous Two-Phase Systems, Chemistry – A European Journal 26, 10987 (2020). J. Spitzberg, X. van Kooten, M. Bercovici, A. Meller, Microfluidic device for coupling isotachophoretic sample focusing with nanopore single-molecule sensing, Nanoscale 12, 17805 (2020). Avenue Jules Bordet 160 16, 1140 Evere - Belgium Phone: +32 2 31 50 800 Fax: +32 2 31 50 801 E-mail: info@kyvobio.be ULTRA Series Cy3 fluorescence filter set designed to provide bright, high-contrast images of Cy3-stained samples. Shipping Information Sitemap, ISO 9001:2015 G-%]w}" "EbU =e\/y;$V()3Pr!I07! Note: If a filter is added to the graph, a new column will appear in the information table at the bottom of the page, labeled "Spillover" with the filter shown in parentheses. Battersby, G.A. H. Koh, X. Wang, S. Myong, Visualizing repetitive diffusion activity of double-strand RNA binding proteins by single molecule fluorescence assays, Methods 105, 109 (2016). 25, 2166 (2014). Chem. Click here to see all available distributors. 3.1 - 300 pg/mL (Cell Culture Supernates, Serum, EDTA Plasma, Heparin Plasma, Citrate Plasma) A cytometry apparatus is provided which may be used with a stationary sample cuvette for analysis of a stationary sample or with a flow sample cuvette for analysis of a flowing sample. c/o Carr Riggs Ingram, 500 Grand Boulevard, Suite 210 Miramar Beach, FL 32550 - USA Tel: +1 850 650 7790 Fax: +1 850 650 4383 E-mail: info@biotrend-usa.com The probe was labeled with the Atto-550 dye. Chen, W.-Y. C. Kim, O.-c. Lee, J.-Y. J. Shah, A. Poruri, O. 1 National Flow Cytometry Resource, Bioscience Division, Los Alamos National Laboratory, Los Alamos, New Mexico, USA. This online tool guides you through flow cytometry panel design, providing a simplified, customizable experience to fit your flow cytometry panel design needs. J.N. M. Sauer, S. Juranek, J. introduction Omega Optical. Tomov et al., Detailed Study of DNA Hairpin Dynamics Using Single-Molecule Fluorescence Assisted by DNA Origami, J. Phys. Le Marois, K. Suhling, D. Richards, A. Zayats, Förster Resonance Energy Transfer inside Hyperbolic Metamaterials, ACS Photonics 5, 4594 (2018). All this results in the ultimate flow cytometry solution for deep immunoprofiling, from 24 . After coupling to a substrate the dye carries a net electrical charge of +1. Infected cells were then analyzed and quantified through MACS flow cytometry (Miltenyi Biotec). JZUDuc^lH(6s MlN.S&~n^cjmC&F Aq,6K7J J* K TlM\%p.%z dk1fPRNWFW@cAX+xWV~ gL1x0Gbj>ZBr a].#C ]uyWV(0zEI t+)rl@;X/V])'m&FU i ATTO 550 is a yellow emitting dye that can be excited by the 532 laser and emission captured by the 585/42 filter. trailer Miller, R. Vogel, P.P.T. The displayed graphs show the normalized intensity of each compound, with the excitation curve being represented by a hollow dotted line, and the emission curve being a solid line, filled in with the color of the instrument laser used. These percentages are automatically calculated for each compound currently on the graph. W. Ye, M. Götz, S. Celiksoy, L. Tüting, C. Ratzke, J. Prasad, J. Ricken, S. Wegner, R. Ahijado-Guzmán, T. Hugel, C. Sönnichsen. ✓ Changing color contrast based on dark backgrounds It exists in vitro as a 240-kDa protein with 23 phycoerythrobilin chromophores per molecule. Irving et al., Reactive centre loop mutants of α-1-antitrypsin reveal position-specific effects on intermediate formation along the polymerization pathway, Biosci. N. Gilat, D. Torchinsky, S. Margalit, Y. Michaeli, S. Avraham, H. Sharim, N. Elkoshi, C. Levy, S. Zirkin, Y. Ebenstein, Rapid Quantification of Oxidation and UV Induced DNA Damage by Repair Assisted Damage Detection-(Rapid RADD), Analytical Chemistry 92, 9887 (2020).           Subscribe Newsletters and Email Updates. [doi: 10.1317/clinchem.2009.128967]. Chem. atto 550 flow cytometry channel Multiple fluorescent proteins can be interrogated with the 4-laser version of the Attune Flow Cytometers. Kaminski et al., Light-inducible molecular beacons for spatiotemporally highly defined activation, Chem. The fluorescence is excited most efficiently in the range 540 - 565 nm. Morning Joe Viewership 2021, Sung, M.-J. Available Conjugates The cells were first labeled with mouse anti-human CD3 antibody and then stained with goat anti-mouse IgG labeled with Compound No. Maximum absorption 601 nm; Maximum fluorescence 627 nm. D. Rutz, Q. Luo, L. Freiburger, T. Madl, V. Kaila, M. Sattler, J. Buchner, A switch point in the molecular chaperone Hsp90 responding to client interaction, Nature Communications 9, 1472 (2018). S. Baliga, C. Murphy, L. Sharon, S. Shenoy, D. Biranthabail, H. Weltman, S. Miller, R. Ramasamy, J. Shah. Atto 550 for fluorescence, ≥90% (HPLC) | Sigma-Aldrich S. Hou, L. Sun et al., Fluorescence correlation spectroscopy analysis for accurate determination of proportion of doubly labeled DNA in fluorescent DNA pool for quantitative biochemical assays, Biosens. F. Panzeri, A. Ingargiola et al., Single-molecule FRET experiments with a red-enhanced custom technology SPAD, Proc. When Did The Hamburger Become Popular, ATTO-550. ATTO-488. C.R. S. Mukherjee, J.-M. Knop, R. Oliva, S. Möbitz, R. Winter, Untangling the interaction of α-synuclein with DNA i-motifs and hairpins by volume-sensitive single-molecule FRET spectroscopy, RSC Chemical Biology 2, 1196 (2021). Atto 550 is a fluorescent compound with an excitation peak at 554 nm and an emission peak at 575 nm. ATTO-550. M. Zoppo, N. Okoniewski, S. Pantelyushin, J. Vom Berg, K. Schirmer, A ribonucleoprotein transfection strategy for CRISPR/Cas9‐mediated gene editing and single cell cloning in rainbow trout cells, Cell & Bioscience 11, 1 (2021). Herr, Microchamber Western Blotting Using Poly L Lysine Conjugated Polyacrylamide Gel for Blotting of Sodium Dodecyl Sulfate Coated Proteins, Anal. E. Favaro, D.R. M. Malle, P. Löffler, S. Bohr, M. Sletfjerding, N. Risgaard, S. Jensen, M. Zhang, P. Hedegård, S. Vogel, N. Hatzakis, Single-particle combinatorial multiplexed liposome fusion mediated by DNA, Nature Chemistry 14, 558 (2022). Path. All Rights Reserved. Changing color contrast based on dark backgrounds Rua Almada Negreiros Lote 5, Loja 14 2615-275 Alverca do Ribatejo - Portugal Tel. An, J. Lee, J. Ryu, R. Hill, D. McIlroy, Y. Kim, D. Choi, Radio frequency-mediated local thermotherapy for destruction of pancreatic tumors using NiAu coreshell nanowires, Nanotechnology 28, 03LT01 (2016). This experiment was performed under reducing conditions using the 12-230 kDa separation system. M. Baibakov, S. Patra, J.-B. 0000032428 00000 n A one parameter histogram plotting channel number vs. number of events. Despite our efforts to enable website browsing for all the website pages, there may be website pages that haven't been made accessible yet or may lack a suitable technical solution. © 2023 Alomone Labs. Kim, G. Krainer, D. Lamb, N. Lee, E. Lemke, B. Levesque, M. Levitus, J. McCann, N. Naredi-Rainer, D. Nettels, T. Ngo, R. Qiu, N. Robb, C. Rcker, H. Sanabria, M. Schlierf, T. Schrder, B. Schuler, H. Seidel, L. Streit, J. Thurn, P. Tinnefeld, S. Tyagi, N. Vandenberk, A. Vera, K. Weninger, B. Wnsch, I. Yanez-Orozco, J. Michaelis, C. Seidel, T. Craggs, T. Hugel. S.R. They are analogous to Alexa dyes and are comparable to any fluorescent technology (and used under license from ATTO-TEC). R. Roy, S. Hohng, T. Ha, A practical guide to single-molecule FRET, Nature Methods 5(6), 2008, 507-516. I. Rutten, D. Daems, J. Lammertyn, Boosting biomolecular interactions through DNA origami nano-tailored biosensing interfaces, Journal of Materials Chemistry B 8, 3606 (2020). ✓ Underlining links throughout the website. Antibody conjugation is a critical step in many molecular-biology research assays. Not for use in diagnostic procedures. flow cytometry, cancer, Attune NxT. Levin, Antibodies to an Intracellular Antigen Penetrate Neuronal Cells and Cause Deleterious Effects, J. Clin. 136, 7771 (2014). Anti-Angiotensin II Receptor Type-1-ATTO Fluor-550 Antibody - Alomone Labs Atto 550 is a new label with high molecular absorption (120,000) and quantum yield (0.80) as well as sufficient Stokes shift between excitation and emission maximum. Maximum absorption 630 nm; Maximum fluorescence 651 nm. introduction Omega Optical. Claude, J. Wenger, Fluorescence Brightness, Photostability, and Energy Transfer Enhancement of Immobilized Single Molecules in Zero-Mode Waveguide Nanoapertures, ACS Photonics 9, 2109 (2022). Lawrie et al., Flow cytometric detection of proteolysis in peptide libraries synthesised on optically encoded supports, Mol. - streptavidin B 110, 1976 (2006). Some fluorochromes (e.g. 0000190962 00000 n The fluorescence is excited most efficiently in the range 610 645 nm. Marks, A. de Magis, H. Kazemier, D. Hilbig, D. Benhalevy, X. Wang, M. Hafner, K. Paeschke, DHX36 prevents the accumulation of translationally inactive mRNAs with G4-structures in untranslated regions, Nature Communications 10, 2421 (2019). Fast acquisition speed is achieved by synchronizing two high-precision pumps for sample mixing, sample injection and probe washing. Intracellular and Plasma Membrane Cholesterol Labeling and ... - PubMed M. Barbiero, S. Castelletto, Q. Zhang, Y. Chen, M. Charnley, S. Russell, M. Gu, Nanoscale magnetic imaging enabled by nitrogen vacancy centres in nanodiamonds labelled by iron-oxide nanoparticles, Nanoscale 12, 8847 (2020). Di Guilmi, S. Marsin, J. Dépagne, X. Veaute, P. Legrand, H. Walbott, J. Vercruyssen, R. Guérois, S. Quevillon-Cheruel, J. Radicella. J. Nikolic, L. Belot, H. Raux, P. Legrand, Y. Gaudin, A. Albertini. - ATTO 550 absorption (.txt), Absorption and Emission Spectrum (graphic) T. Thumberger, T. Tavhelidse-suck, J. Gutierrez-triana, A. Cornean, R. Medert, B. Welz, M. Freichel, J. Wittbrodt. (d) Overlay of the three components. S. Amiar, M. Husby, K. Wijesinghe, S. Angel, N. Bhattarai, B. Gerstman, P. Chapagain, S. Li, R. Stahelin, Lipid-specific oligomerization of the Marburg virus matrix protein VP40 is regulated by two distinct interfaces for virion assembly, Journal of Biological Chemistry 296, 100796 (2021). E. Britt, J. Lika, M. Giese, T. Schoen, G. Seim, Z. Huang, P. Lee, A. Huttenlocher, J. Tomov, R. Tsukanov et al., Rational Design of DNA Motors: Fuel Optimization through Single-Molecule Fluorescence, J. Series 3, e71 (2011). J. Nikolic, L. Belot, H. Raux, P. Legrand, Y. Gaudin, A. Albertini, Structural basis for the recognition of LDL-receptor family members by VSV glycoprotein, Nature Communications 9, 1029 (2018). R. Schoch, I. Barel, F. Brown, G. Haran, Lipid diffusion in the distal and proximal leaflets of supported lipid bilayer membranes studied by single particle tracking, The Journal of Chemical Physics 148, 123333 (2018). M. Jahn, A. Rehn et al., The charged linker of the molecular chaperone Hsp90 modulates domain contacts and biological function, PNAS 111, 17881 (2014). Webinar. Search P. Comba, A. Eisenschmidt, L. Gahan, D.P. to our Newsletters and Email Updates. - maleimide PhenoCycler-Fusion (CODEX)® can detect over 40 biomarkers in an automated cyclical image acquisition process. White, A. Two levels of system alignment are . 42, 252 (2012). Á. Molinero-Fernández, M. Moreno-Guzmán, L. Arruza, M. López, A. Escarpa, Polymer-Based Micromotor Fluorescence Immunoassay for On-the-Move Sensitive Procalcitonin Determination in Very Low Birth Weight Infants’ Plasma, ACS Sensors 5, 1336 (2020). Starbound Weapon Tiers, Maximum absorption 593 nm; Maximum fluorescence 622 nm. 0000196962 00000 n 0000096953 00000 n Figure 3. Z. Lui, F. Galli et al., Stable Single-Walled Carbon Nanotube – Streptavidin Complex for Biorecognition, J. Phys. They are analogous to Alexa dyes and are comparable to any fluorescent technology (and used under license from ATTO-TEC). Flow cytometry provides a well-established method to identify cells in solution and is most commonly used for evaluating peripheral blood, bone marrow, and other body fluids. Multiple fluorescent proteins can be interrogated with the 4-laser version of the Attune Flow Cytometers. Written by Tim Bushnell, PhD. Sung, M.-J. Click "Show Crosshairs" under the "Analyze" submenu in order to trace the exact curve of the currently-selected compounds" fluorescent intensity across the horizontal axis. The choice currently selected will be highlighted in blue. J. de Torres, M. Mivelle, S. Moparthi, H. Rigneault, N. van Hulst, M. Garcia-Parajo, E. Margeat, J. Wenger, Plasmonic Nanoantennas Enable Forbidden Forster Dipole-Dipole Energy Transfer and Enhance the FRET Efficiency, Nano letters 16, 6222 (2016). Shan, A protean clamp guides membrane targeting of tail-anchored proteins, Proceedings of the National Academy of Sciences 114, E8585-E8594 (2017). This label is related to the well known dye Rhodamine 6G and can be used with filters typically used to detect Rhodamine. A. Reinhardt, M. Horn et al., Novel Imidazolium Salt−Peptide Conjugates and Their Antimicrobial Activity, Bioconjugate Chem. ✓ Adapting the website to color blind people The Atto dyes are a series of fluorescent dyes that meet the critical needs of modern fluorescent technologies: Stability - Atto 655 and Atto 647N are photostable and highly resistant to ozone degradation, making them ideal for microarray applications. S. Braun, C. Humphreys et al., Amyloid-Associated Nucleic Acid Hybridisation, PLoS ONE 6, e19125 (2011). Shipping costs, Terms and Conditions The antibody can be used in western blot, immunocytochemistry, immunohistochemistry, and indirect flow cytometry applications. Click here to see all available distributors. 14, 4707 (2014). J. Reyes, S. Ekmark-Léwen, M. Perdiki, T. Klingstedt, A. Hoffmann, E. Wiechec, P. Nilsson, K. Nilsson, I. Alafuzoff, M. Ingelsson, M. Hallbeck, Accumulation of alpha-synuclein within the liver, potential role in the clearance of brain pathology associated with Parkinson's disease, Acta neuropathologica communications 9, 46 (2021). The CD4+CD25+(high) gating strategy shown here was used to identify Treg populations. Both proteins contain fluorescent phycobilin chromophores embedded into a protein scaffolding which accounts for their large size. D. Hastman, J. Melinger, G. Aragons, P. Cunningham, M. Chiriboga, Z. Salvato, T. Salvato, C. Brown, D. Mathur, I. Medintz, E. Oh, S. Daz, Femtosecond Laser Pulse Excitation of DNA-Labeled Gold Nanoparticles, ACS Nano (2020). All rights reserved. Anti-Aquaporin 2/AQP2-ATTO Fluor-550 Antibody | Alomone Labs Reagent Selection Guide for the Attune Flow Cytometers. P. Ghenuche, J. de Torres et al., Nanophotonic Enhancement of the Forster Resonance Energy-Transfer Rate with Single Nanoapertures, Nano Lett. Surawski, B.J. Z. Tang, Q. Wei, A. Wie, Metal-Mesh Litography, Appl. Within our portfolio, we gladly take on special requests for: ✓ Customized antibody labeling J. Spitzberg, X. van Kooten, M. Bercovici, A. Meller, Microfluidic device for coupling isotachophoretic sample focusing with nanopore single-molecule sensing, Nanoscale 12, 17805 (2020). Products for Flow Cytometry CF Dyes for Flow Cytometer Laser Lines 2 More photostable and less spill over in the 525/50 green channel than Pacific ATTO 550, Cy3, DyLight 549, TRITC Brighter than Cy3 Comparable to Alexa Fluor 555 Green (532 nm). For Research Use Only. 0 EP2211174A2 EP10158606A EP10158606A EP2211174A2 EP 2211174 A2 EP2211174 A2 EP 2211174A2 EP 10158606 A EP10158606 A EP 10158606A EP 10158606 A EP10158606 A EP 10158606A EP 2211174 A2 EP2211174 A2 EP 2211174A2 Authority EP European Patent Office Prior art keywords particles polymer particles multicolored heterogenous dyes Prior art date 2005-07-11 Legal status FIG. J. de Torres, M. Mivelle, S. Moparthi, H. Rigneault, N. van Hulst, M. Garcia-Parajo, E. Margeat, J. Wenger, Plasmonic Nanoantennas Enable Forbidden Forster Dipole-Dipole Energy Transfer and Enhance the FRET Efficiency, Nano letters 16, 6222 (2016). . If you ownour legacyBDLSR II Flow Cytometer,you can take advantage of ourexclusive special offers for trading in yourBDLSR IISystem. Chem. B. Agrawalla, T. Wang, A. Riegger, M. Domogalla, K. Steinbrink, T. Dörfler, X. Chen, F. Boldt, M. Lamla, J. Michaelis, S. Kuan, T. Weil, Chemoselective Dual Labeling of Native and Recombinant Proteins, Bioconjugate Chemistry 29, 29 (2018). R. Masoud, R. Tsukanov et al., Studying the Structural Dynamics of Bipedal DNA Motors with Single-Molecule Fluorescence Spectroscopy, ACS Nano 6, 6272 (2012). W. Ye, M. Götz, S. Celiksoy, L. Tüting, C. Ratzke, J. Prasad, J. Ricken, S. Wegner, R. Ahijado-Guzmán, T. Hugel, C. Sönnichsen, Conformational Dynamics of a Single Protein Monitored for 24 h at Video Rate, Nano letters 18, 6633 (2018). Claude, A. Moreau, J. Lumeau, J. Wenger, Extending Single-Molecule Förster Resonance Energy Transfer (FRET) Range beyond 10 Nanometers in Zero-Mode Waveguides, ACS Nano 13, 8469 (2019). Displays the excitation and emission profiles of the fluorophores available to you, essential when building multicolor panels for flow cytometry . Fluorescent microscopy of human skin tissue section (paraffin fixation) with fungal infection.
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