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Chemical tags: Applications in live cell fluorescence imaging

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Site‐Specific Protein Modification on Living Cells Catalyzed by Sortase
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Fluorescent labeling of proteins in living cells using the FKBP12 (F36V) tag
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The protein-labeling reagent FLASH-EDT 2 binds not only to CCXXCC motifs but also non-specifically to endogenous cysteine-rich proteins
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In Vivo Labeling Method Using a Genetic Construct for Nanoscale Resolution Microscopy
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Measuring calcium dynamics in living cells with genetically encodable calcium indicators
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Ligand-directed tosyl chemistry for protein labeling in vivo
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Selective destruction of protein function by chromophore-assisted laser inactivation.
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Redesigning an FKBP–ligand interface to generate chemical dimerizers with novel specificity
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Fluorescence microscopy with diffraction resolution barrier broken by stimulated emission
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Histidine 289 Is Essential for Hydrolysis of the Alkyl-enzyme Intermediate of Haloalkane Dehalogenase
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Genetically Encoded Indicators of Cellular Calcium Dynamics Based on Troponin C and Green Fluorescent Protein
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Myosin V Walks Hand-Over-Hand: Single Fluorophore Imaging with 1.5-nm Localization
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Kinesin Walks Hand-Over-Hand
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The Fluorescent Toolbox for Assessing Protein Location and Function
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Imaging Intracellular Fluorescent Proteins at Nanometer Resolution
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Far-Field Optical Nanoscopy
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Multicolor Super-Resolution Imaging with Photo-Switchable Fluorescent Probes
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Probing Immunosuppressant Action with a Nonnatural Immunophilin Ligand
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Specific Covalent Labeling of Recombinant Protein Molecules Inside Live Cells
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Controlling Signal Transduction with Synthetic Ligands
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Green Fluorescent Protein as a Marker for Gene Expression
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Dynamic Fluorescent Imaging of Human Immunodeficiency Virus Type 1 Gag in Live Cells by Biarsenical Labeling
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Superresolution Imaging using Single-Molecule Localization
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Advances in fluorescent protein technology
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Cytoskeletal coherence requires myosin-IIA contractility
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Fluorophores for live cell imaging of AGT fusion proteins across the visible spectrum
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Direct pH Measurements by using Subcellular Targeting of 5(and 6-) Carboxyseminaphthorhodafluor in Mammalian Cells

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1128/mbio.02172-14openalex-snapshot
Superresolution Imaging Captures Carbohydrate Utilization Dynamics in Human Gut Symbionts
inferred← citeshttps://doi.org/10.1134/s1068162017030074openalex-snapshot
Fluorophores for single-molecule localization microscopy
inferred← citeshttps://doi.org/10.1146/annurev-physchem-032811-112012openalex-snapshot
Live-Cell Super-Resolution Imaging with Synthetic Fluorophores
inferred← citeshttps://doi.org/10.13070/mm.cn.2.124openalex-snapshot
活细胞成像方法回顾
inferred← citeshttps://doi.org/10.13070/mm.en.2.124openalex-snapshot
Live Cell Imaging Methods Review
inferred← citeshttps://doi.org/10.1371/journal.pone.0036314openalex-snapshot
Live Imaging of Mitosomes and Hydrogenosomes by HaloTag Technology
inferred← citeshttps://doi.org/10.1371/journal.pone.0106271openalex-snapshot
Evaluation of Chemical Fluorescent Dyes as a Protein Conjugation Partner for Live Cell Imaging
inferred← citeshttps://doi.org/10.1371/journal.pone.0113708openalex-snapshot
Site-Specific Labeling of Neurotrophins and Their Receptors via Short and Versatile Peptide Tags
inferred← citeshttps://doi.org/10.3389/fimmu.2023.1204730openalex-snapshot
Virus tracking technologies and their applications in viral life cycle: research advances and future perspectives
inferred← citeshttps://doi.org/10.3389/fphys.2014.00273openalex-snapshot
Nano-scale measurement of biomolecules by optical microscopy and semiconductor nanoparticles
inferred← citeshttps://doi.org/10.3390/ijms16011949openalex-snapshot
Ligand-Induced Dynamics of Neurotrophin Receptors Investigated by Single-Molecule Imaging Approaches
inferred← citeshttps://doi.org/10.3390/ijms232314949openalex-snapshot
Choosing the Probe for Single-Molecule Fluorescence Microscopy
inferred← citeshttps://doi.org/10.3390/molecules29153596openalex-snapshot
β-Galactosidase- and Photo-Activatable Fluorescent Probes for Protein Labeling and Super-Resolution STED Microscopy in Living Cells
inferred← citeshttps://doi.org/10.53846/goediss-5450openalex-snapshot
Non-Canonical Amino Acids as Minimal Tags for Investigating Protein Organization and Turnover
inferred← citeshttps://doi.org/10.70675/077168b5z9a57z46f4z8a9czf9513c047f5aopenalex-snapshot
Développement de conjugués peptidiques fluorocarbonés pour augmenter la stabilité plasmatique de peptides visant des récepteurs couplés aux protéines G
inferred← citeshttps://doi.org/10.70675/0e5c459czb459z4691z92afz9ffdfe7da161openalex-snapshot
Développement de sondes polymères fluorescentes à propriétés de ciblage améliorées pour des applications en imagerie cellulaire et en oncologie
inferred← citeshttps://doi.org/10.70675/4f0b3f5az13e1z4fc3zbe91z48a4e48e83fdopenalex-snapshot
Essential cytoplasmic role(s) of the "histone" lysine methyltransferase Setdb1 in post-transcriptional regulation of gene expression
inferred← citeshttps://doi.org/10.70675/af62f018z7c1az4348z932dzfbd90558bb78openalex-snapshot
Conception, synthesis and evaluation of fluorescent probes and PET radioligands for the oxytocin and vasopressin receptors
inferred← citeshttps://doi.org/10.7868/s0132342317030083openalex-snapshot
ФЛУОРОФОРЫ ДЛЯ ЛОКАЛИЗАЦИОННОЙ МИКРОСКОПИИ ОДИНОЧНЫХ МОЛЕКУЛ, "Биоорганическая химия"
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.