The protein-labeling reagent FLASH-EDT2 binds not only to CCXXCC motifs but also non-specifically to endogenous cysteine-rich proteins.
about
Computational design of a red fluorophore ligase for site-specific protein labeling in living cellsFluorophore targeting to cellular proteins via enzyme-mediated azide ligation and strain-promoted cycloadditionImaging proteins inside cells with fluorescent tagsBioorthogonal chemistry: fishing for selectivity in a sea of functionalityA fluorophore ligase for site-specific protein labeling inside living cellsArsenic binding to proteinsNovel peptide sequence ("IQ-tag") with high affinity for NIR fluorochromes allows protein and cell specific labeling for in vivo imagingLabeling of multiple HIV-1 proteins with the biarsenical-tetracysteine systemΠ-Clamp-mediated cysteine conjugationTetracysteine-based fluorescent tags to study protein localization and trafficking in Plasmodium falciparum-infected erythrocytesAn arsenic fluorescent compound as a novel probe to study arsenic-binding proteins.Specific and covalent labeling of a membrane protein with organic fluorochromes and quantum dotsSpecific biarsenical labeling of cell surface proteins allows fluorescent- and biotin-tagging of amyloid precursor protein and prion proteins.Rabies virus envelope glycoprotein targets lentiviral vectors to the axonal retrograde pathway in motor neurons.A SNAP-tagged derivative of HIV-1--a versatile tool to study virus-cell interactions.A general approach for chemical labeling and rapid, spatially controlled protein inactivation.Multiphoton excitation-evoked chromophore-assisted laser inactivation using green fluorescent protein.Fluorophore-assisted light inactivation produces both targeted and collateral effects on N-type calcium channel modulation in rat sympathetic neurons.Phage display evolution of a peptide substrate for yeast biotin ligase and application to two-color quantum dot labeling of cell surface proteins.Chemical rescue of protein tyrosine phosphatase activity.Chemical biology-based approaches on fluorescent labeling of proteins in live cells.Site-specific labeling of the type 1 ryanodine receptor using biarsenical fluorophores targeted to engineered tetracysteine motifsFluorescent labeling of tetracysteine-tagged proteins in intact cellsTargeting a cryptic allosteric site for selective inhibition of the oncogenic protein tyrosine phosphatase Shp2Multivalency in the inhibition of oxidative protein folding by arsenic(III) species.Rapid labeling of intracellular His-tagged proteins in living cells.A fusion of disciplines: chemical approaches to exploit fusion proteins for functional genomics.Intramolecular ex vivo Fluorescence Resonance Energy Transfer (FRET) of Dihydropyridine Receptor (DHPR) β1a Subunit Reveals Conformational Change Induced by RYR1 in Mouse Skeletal MyotubesSpecific inhibition of sensitized protein tyrosine phosphatase 1B (PTP1B) with a biarsenical probeThe Burkholderia pseudomallei Proteins BapA and BapC Are Secreted TTSS3 Effectors and BapB Levels Modulate Expression of BopE.Bichromophoric dyes for wavelength shifting of dye-protein fluoromodules.Selective photoinactivation of protein function through environment-sensitive switching of singlet oxygen generation by photosensitizer.Single-cell FRET imaging of transferrin receptor trafficking dynamics by Sfp-catalyzed, site-specific protein labeling.Fluorescence Resonance Energy Transfer-based Structural Analysis of the Dihydropyridine Receptor α1S Subunit Reveals Conformational Differences Induced by Binding of the β1a Subunit.Cross-strand split tetra-Cys motifs as structure sensors in a beta-sheet protein.Selective recognition of protein tetraserine motifs with a cell-permeable, pro-fluorescent bis-boronic acid.Selective labeling of proteins with chemical probes in living cells.Application of metal coordination chemistry to explore and manipulate cell biology.Imaging the boundaries-innovative tools for microscopy of living cells and real-time imaging.Tracking the green invaders: advances in imaging virus infection in plants.
P2860
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P2860
The protein-labeling reagent FLASH-EDT2 binds not only to CCXXCC motifs but also non-specifically to endogenous cysteine-rich proteins.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh
2001年學術文章
@zh-hant
name
The protein-labeling reagent F ...... genous cysteine-rich proteins.
@en
type
label
The protein-labeling reagent F ...... genous cysteine-rich proteins.
@en
prefLabel
The protein-labeling reagent F ...... genous cysteine-rich proteins.
@en
P2093
P356
P1433
P1476
The protein-labeling reagent F ...... genous cysteine-rich proteins.
@en
P2093
P2888
P304
P356
10.1007/S004240100619
P577
2001-09-01T00:00:00Z