Alexa Fluor™ 647 Alkyne, Triethylammonium Salt
Alexa Fluor™ 647 Alkyne, Triethylammonium Salt
Citations & References (4)
Invitrogen™

Alexa Fluor™ 647 Alkyne, Triethylammonium Salt

The far red-fluorescent Alexa Fluor® 647 alkyne is reactive with azides via a copper-catalyzed click reaction. The bright and photostableRead more
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Catalog NumberQuantity
A102780.5 mg
Catalog number A10278
Price (KRW)
689,000
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Ends: 31-Dec-2025
861,000
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Quantity:
0.5 mg
Price (KRW)
689,000
Online offer
Ends: 31-Dec-2025
861,000
Save 172,000 (20%)
Each
Add to cart
The far red-fluorescent Alexa Fluor® 647 alkyne is reactive with azides via a copper-catalyzed click reaction. The bright and photostable fluorophore can be for used with flow cytometry, microscopy and HCS
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Chemical ReactivityAzide
Detection MethodFluorescence
FormatSolid
Label or DyeAlexa Fluor™ 647
Product TypeAlkyne
Quantity0.5 mg
Reactive GroupAlkyne
Reactive MoietyAlkyne
Shipping ConditionRoom Temperature
SolubilityDMSO (Dimethylsulfoxide)
ColorFar-red
Label TypeAlexa Fluor
Product LineAlexa Fluor, Molecular Probes
Unit SizeEach
Contents & Storage
Store at ≤-20°C, desiccated and protect from light.

Citations & References (4)

Citations & References
Abstract
Dynamic monitoring of newly synthesized proteomes: up-regulation of myristoylated protein kinase A during butyric acid induced apoptosis.
Authors:Liu K, Yang PY, Na Z, Yao SQ,
Journal:Angew Chem Int Ed Engl
PubMed ID:21678537
Doubly charged: A double metabolic incorporation approach capable of proteome-wide profiling of post-translational modification dynamics on newly synthesized proteins has been developed (see scheme; blue box: methionine surrogate, orange diamond: PTM probe). This strategy reveals for the first time that up-regulation of myristoylated PKA protein is necessary for the occurrence ... More
Identification of a novel prenyl and palmitoyl modification at the CaaX motif of Cdc42 that regulates RhoGDI binding.
Authors:Nishimura A, Linder ME,
Journal:Mol Cell Biol
PubMed ID:23358418
Membrane localization of Rho GTPases is essential for their biological functions and is dictated in part by a series of posttranslational modifications at a carboxyl-terminal CaaX motif: prenylation at cysteine, proteolysis of the aaX tripeptide, and carboxymethylation. The fidelity and variability of these CaaX processing steps are uncertain. The brain-specific ... More
A multifunctional bioconjugate module for versatile photoaffinity labeling and click chemistry of RNA.
Authors:Kellner S, Seidu-Larry S, Burhenne J, Motorin Y, Helm M,
Journal:Nucleic Acids Res
PubMed ID:21646334
A multifunctional reagent based on a coumarin scaffold was developed for derivatization of naive RNA. The alkylating agent N3BC [7-azido-4-(bromomethyl)coumarin], obtained by Pechmann condensation, is selective for uridine. N3BC and its RNA conjugates are pre-fluorophores which permits controlled modular and stepwise RNA derivatization. The success of RNA alkylation by N3BC ... More
Site-specific terminal and internal labeling of RNA by poly(A) polymerase tailing and copper-catalyzed or copper-free strain-promoted click chemistry.
Authors:Winz ML, Samanta A, Benzinger D, Jäschke A,
Journal:Nucleic Acids Res
PubMed ID:22344697
The modification of RNA with fluorophores, affinity tags and reactive moieties is of enormous utility for studying RNA localization, structure and dynamics as well as diverse biological phenomena involving RNA as an interacting partner. Here we report a labeling approach in which the RNA of interest--of either synthetic or biological ... More