Alexa Fluor™ 488 Cadaverine
Alexa Fluor™ 488 Cadaverine
Invitrogen™

Alexa Fluor™ 488 Cadaverine

Alexa Fluor™ 488 Cadaverine is useful as a polar tracer and as a reactive dye for labeling proteins via aRead more
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Catalog NumberQuantity
A306761 mg
Catalog number A30676
Price (EUR)
504,00
Each
Add to cart
Quantity:
1 mg
Price (EUR)
504,00
Each
Add to cart

Alexa Fluor™ 488 Cadaverine is useful as a polar tracer and as a reactive dye for labeling proteins via a carboxylic acid moiety. Alexa Fluor™ 488 is a bright, green-fluorescent dye with excitation ideally suited to the 488 nm laser line. Used for stable signal generation in imaging and flow cytometry, Alexa Fluor™ 488 dye is water soluble and pH-insensitive from pH 4 to pH 10. In addition to reactive dye formulations, we offer Alexa Fluor™ 488 dye conjugated to a variety of antibodies, peptides, proteins, tracers, and amplification substrates optimized for cellular labeling and detection (learn more).

Detailed information about this AlexaFluor™ cadaverine:
• Fluorophore label : Alexa Fluor™ 488 dye
• Reactive group: cadaverine
• Reactivity: carboxylic acids, aldehydes, and ketones (and glutamine residues through an enzyme-catalyzed transamidation reaction)
• Ex/Em of the conjugate: 493/516 nm
• Extinction coefficient: 73,000 M-1cm-1
• Spectrally similar dyes: FITC, GFP
• Molecular weight: 640.61 g/mol

Cell Tracking and Tracing Applications
Alexa Fluor™ cadaverines make excellent fluorescent polar tracers because they are bright, small, and water soluble. Since they contain an aldehyde-fixable functional group, they can be fixed in cells by treatment with formaldehyde or glutaraldehyde. They are easily loaded into cells by microinjection, infusion from patch pipette, or uptake induced by our Influx™ Pinocytic Cell-Loading Reagent. Learn more about cell tracking and tracing.

Protein Labeling Applications
Alexa Fluor™ cadaverines can be used as reactive molecules for adding a fluorescent label to carboxylic acids using a coupling agent such as a carbodiimide; they do not spontaneously react with carboxylic acids in solution. They do, however, react spontaneously with the common amine-reactive functional groups, including succinimidyl esters and isothiocyanates. The amine-containing Alexa Fluor™ cadaverines can also be used to label glutamine residues in some proteins and peptides via an enzyme-catalyzed transamidation reaction.

Learn More About Protein and Antibody Labeling
We offer a wide selection of Molecular Probes™ antibody and protein labeling kits to fit your starting material and your experimental setup. See our Antibody Labeling kits or use our Labeling Chemistry Selection Tool for other choices. To learn more about our labeling kits, read Kits for Labeling Proteins and Nucleic Acids—Section 1.2 in The Molecular Probes™ Handbook.

We’ll Make a Custom Conjugate for You
If you can’t find what you’re looking for in our online catalog, we’ll prepare a custom antibody or protein conjugate for you. Our custom conjugation service is efficient and confidential, and we stand by the quality of our work. We are ISO 13485:2000 certified.

Dissolve in water to prepare a stock concentrations of 1 to 10 mg/mL.

Related Products
DMSO (dimethylsulfoxide)
Antibody Conjugate Purification Kit for 0.5–1 mg
Antibody Conjugate Purification Kit for 20–50 μg
Antibody Conjugate Purification kit for 50–100 μg

For Research Use Only. Not for use in diagnostic procedures.
Specifications
Chemical ReactivityCarboxylic Acid, Ketone, Aldehyde
Emission516 nm
Excitation493 nm
Label or DyeAlexa Fluor™ 488
Molecular Weight (g/mol)640.61 g/mol
Product TypeCadaverine
Quantity1 mg
Reactive MoietyAmine, Cadaverine
Shipping ConditionRoom Temperature
Label TypeAlexa Fluor
Product LineAlexa Fluor
Unit SizeEach
Contents & Storage
Store in freezer (-5°C to -30°C) and protect from light.

Citations & References (8)

Citations & References
Abstract
Optical properties of Alexa 488 and Cy5 immobilized on a glass surface.
Authors:Wang L, Gaigalas AK, Reipa V
Journal:Biotechniques
PubMed ID:15679095
'The absorption and emission spectra were measured for Cy5 and Alexa 488 fluorophores confined on a glass surface. The data were obtained using fluorometry and spectroscopic ellipsometry. Red shifts of the surface-immobilized fluorophore absorption spectra relative to the fluorophore spectra in aqueous solution were observed using both methods. We interpret ... More
Visualization of galectin-3 oligomerization on the surface of neutrophils and endothelial cells using fluorescence resonance energy transfer.
Authors:Nieminen J, Kuno A, Hirabayashi J, Sato S
Journal:J Biol Chem
PubMed ID:17082191
'Galectin-3, a member of the galectin family of carbohydrate binding proteins, is widely expressed, particularly in cells involved in the immune response. Galectin-3 has also been indicated to play a role in various biological activities ranging from cell repression to cell activation and adhesion and has, thus, been recognized as ... More
The obligatory role of the actin cytoskeleton on inward remodeling induced by dithiothreitol activation of endogenous transglutaminase in isolated arterioles.
Authors:Castorena-Gonzalez JA, Staiculescu MC, Foote CA, Polo-Parada L, Martinez-Lemus LA,
Journal:
PubMed ID:24337457
Inward remodeling is the most prevalent structural change found in the resistance arteries and arterioles of hypertensive individuals. Separate studies have shown that the inward remodeling process requires transglutaminase activation and the polymerization of actin. Therefore, we hypothesize that inward remodeling induced via endogenous transglutaminase activation requires and depends on ... More
Autophagy and protein kinase C are required for cardioprotection by sulfaphenazole.
Authors:Huang C, Liu W, Perry CN, Yitzhaki S, Lee Y, Yuan H, Tsukada YT, Hamacher-Brady A, Mentzer RM, Gottlieb RA,
Journal:Am J Physiol Heart Circ Physiol
PubMed ID:20008275
Previously, we showed that sulfaphenazole (SUL), an antimicrobial agent that is a potent inhibitor of cytochrome P4502C9, is protective against ischemia-reperfusion (I/R) injury (Ref. 15). The mechanism, however, underlying this cardioprotection, is largely unknown. With evidence that activation of autophagy is protective against simulated I/R in HL-1 cells, and evidence ... More
Whole-cell 3D STORM reveals interactions between cellular structures with nanometer-scale resolution.
Authors:Huang B, Jones SA, Brandenburg B, Zhuang X,
Journal:Nat Methods
PubMed ID:19029906
The ability to directly visualize nanoscopic cellular structures and their spatial relationship in all three dimensions will greatly enhance our understanding of molecular processes in cells. Here we demonstrated multicolor three-dimensional (3D) stochastic optical reconstruction microscopy (STORM) as a tool to quantitatively probe cellular structures and their interactions. To facilitate ... More