The Click-iT™ ManNAz metabolic glycoprotein labeling reagent provides the first part of a simple and robust two-step technique to identifyRead more
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Catalog Number
Quantity
C33366
5.2 mg
Catalog number C33366
Price (KRW)
539,000
Exklusiv online
Ends: 31-Dec-2025
673,000
Save 134,000 (20%)
Each
Add to cart
Quantity:
5.2 mg
Price (KRW)
539,000
Exklusiv online
Ends: 31-Dec-2025
673,000
Save 134,000 (20%)
Each
Add to cart
The Click-iT™ ManNAz metabolic glycoprotein labeling reagent provides the first part of a simple and robust two-step technique to identify and characterize cell surface sialic acid-containing glycoproteins. In step one, cultured cells are incubated with the azide-modified mannosamine (ManNAz). The azido-sugar is metabolically incorporated into cell surface sialic acid-containing glycoproteins through the permissive nature of the oligosaccharide biosynthesis pathway,. In step two, via the chemoselective ligation or click reaction between an azide and an alkyne, the azido-labeled glycoproteins can then be detected with a Click-iT™ Glycoprotein Detection kit for gels (TAMRA or Dapoxyl™ alkyne) or Western blots (biotin alkyne). These Click-iT™ products are compatible with LC-MS⁄MS and Multiplexed Proteomics™ technologies for in-depth analyses of the glycoproteome.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Detection MethodBiotin-based, Fluorescence
Green FeaturesLess hazardous
Product LineClick-iT
Product TypeLabeling Reagent
Quantity5.2 mg
Shipping ConditionRoom Temperature
Labeling TargetProteins
Label or DyeAlexa Fluor 488, Alexa Fluor 555, Alexa Fluor 594, Alexa Fluor 647, Biotin, Oregon Green 488, TMR (Tetramethylrhodamine)
Unit SizeEach
Contents & Storage
Store in freezer -5°C to -30°C.
Citations & References (7)
Citations & References
Abstract
Metabolic labeling of glycans with azido sugars for visualization and glycoproteomics.
Authors:Laughlin ST, Agard NJ, Baskin JM, Carrico IS, Chang PV, Ganguli AS, Hangauer MJ, Lo A, Prescher JA, Bertozzi CR,
Journal:Methods Enzymol
PubMed ID:17116478
'The staggering complexity of glycans renders their analysis extraordinarily difficult, particularly in living systems. A recently developed technology, termed metabolic oligosaccharide engineering, enables glycan labeling with probes for visualization in cells and living animals, and enrichment of specific glycoconjugate types for proteomic analysis. This technology involves metabolic labeling of glycans ... More
Copper-free click chemistry for highly luminescent quantum dot conjugates: application to in vivo metabolic imaging.
Authors:Bernardin A, Cazet A, Guyon L, Delannoy P, Vinet F, Bonnaffé D, Texier I,
Journal:Bioconjug Chem
PubMed ID:20222737
Quantum dots (QD) are inorganic nanocrystals with outstanding optical properties, specially suited for biological imaging applications. Their attachment to biomolecules in mild aqueous conditions for the design of bioconjugates is therefore highly desirable. 1,3-dipolar [3 + 2] cycloaddition between azides and terminal alkynes ( ... More
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
Sialic Acids Attached to O-Glycans Modulate Voltage-gated Potassium Channel Gating.
Authors:Schwetz TA, Norring SA, Ednie AR, Bennett ES,
Journal:J Biol Chem
PubMed ID:21115483
Neuronal, cardiac, and skeletal muscle action potentials are produced and conducted through the highly regulated activity of several types of voltage-gated ion channels. Voltage-gated potassium (K(v)) channels are responsible for action potential repolarization. Glycans can be attached to glycoproteins through N- and O-linkages. Previous reports described the impact of N-glycans ... More
A FRET-based fluorogenic phosphine for live-cell imaging with the Staudinger ligation.
Authors:Hangauer MJ, Bertozzi CR,
Journal:Angew Chem Int Ed Engl
PubMed ID:18306205
Fluorescent phosphine probes have been used for direct imaging of various azide-bearing biomolecules with the Staudinger ligation in cell-free environments. Recently, we applied phosphine-based dyes to image azides on the surface of live cells. Notably, significant labeling above background could only be achieved using a highly negatively charged ... More