Alexa Fluor™ 555 C2 Maleimide
Alexa Fluor&trade; 555 C<sub>2</sub> Maleimide
Invitrogen™

Alexa Fluor™ 555 C2 Maleimide

Alexa Fluor™ 555 is a bright orange dye. Used for stable signal generation in imaging and flow cytometry, Alexa Fluor™Read more
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Catalog NumberQuantity
A203461 mg
Catalog number A20346
Price (KRW)
494,000
Online offer
Ends: 31-Dec-2025
617,000
Save 123,000 (20%)
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Quantity:
1 mg
Price (KRW)
494,000
Online offer
Ends: 31-Dec-2025
617,000
Save 123,000 (20%)
Each
Add to cart
Alexa Fluor™ 555 is a bright orange dye. Used for stable signal generation in imaging and flow cytometry, Alexa Fluor™ 555 dye is water soluble and pH-insensitive from pH 4 to pH 10. In addition to reactive dye formulations, we offer Alexa Fluor™ 555 dye conjugated to a variety of antibodies, peptides, proteins, tracers, and amplification substrates optimized for cellular labeling and detection (learn more).

The maleimide derivative of Alexa Fluor™ 555 is the most popular tool for conjugating the dye to a thiol group on a protein, oligonucleotide thiophosphate, or low molecular weight ligand. The resulting Alexa Fluor™ 555 conjugates exhibit brighter fluorescence and greater photostability than the conjugates of other spectrally similar fluorophores.

Detailed information about this AlexaFluor™ maleimide:

Fluorophore label: Alexa Fluor™ 555 dye
Reactive group: maleimide
Reactivity: thiol groups on proteins and ligands, oligonucleotide thiophosphates
Ex/Em of the conjugate: 556/572 nm
Extinction coefficient: 158,000 cm-1M-1
Spectrally similar dyes: Tetramethylrhodamine
Molecular weight: ∼1250

Typical Conjugation Reaction
The protein should be dissolved at a concentration of 50-100 μM in a suitable buffer (10-100 mM phosphate, Tris, or HEPES) at pH 7.0-7.5. In this pH range, the protein thiol groups are sufficiently nucleophilic that they react almost exclusively with the reagent in the presence of the more numerous protein amine groups, which are protonated and relatively unreactive. We recommend reducing any disulfide bonds at this point using a 10-fold molar excess of reducing agent such as DTT or TCEP. Excess DTT must be removed by dialysis and subsequent thiol-modification should be carried out under oxygen-free conditions to prevent reformation of the disulfide bonds; these precautions are not necessary when using TCEP prior to maleimide conjugation.

The Alexa Fluor™ maleimide is typically dissolved in high-quality anhydrous dimethylsulfoxide (DMSO) at a concentration of 1-10 mM immediately prior to use, and stock solutions should be protected from light as much as possible. Generally, this stock solution is added to the protein solution dropwise while stirring to produce approximately 10-20 moles of reagent per mole of protein, and the reaction is allowed to proceed at room temperature for 2 hours or at 4°C overnight, protected from light. Any unreacted thiol-reactive reagent can be consumed by adding excess glutathione, mercaptoethanol, or other soluble low molecular weight thiol.

Conjugate Purification
Labeled antibodies are typically separated from free Alexa Fluor™ dye using a gel filtration column, such as Sephadex™ G-25, BioGel™ P-30, or equivalent. For much larger or smaller proteins, select a gel filtration media with an appropriate molecular weight cut-off or purify by dialysis. We offer several purification kits optimized for different quantities of antibody conjugate:
Antibody Conjugate Purification Kit for 0.5-1 mg (A33086)
Antibody Conjugate Purification Kit for 20-50 μg (A33087)
Antibody Conjugate Purification kit for 50-100 μg (A33088)

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.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Chemical ReactivityThiol
Emission572 nm
Excitation556 nm
Label or DyeAlexa Fluor™ 555
Product TypeDye
Quantity1 mg
Reactive MoietyMaleimide
Shipping ConditionRoom Temperature
Label TypeAlexa Fluor
Product LineAlexa Fluor
Unit SizeEach
Contents & Storage
Store in freezer (-5 to -30°C) and protect from light.

Citations & References (10)

Citations & References
Abstract
Single-molecule investigation of the T4 bacteriophage DNA polymerase holoenzyme: multiple pathways of holoenzyme formation.
Authors:Smiley RD, Zhuang Z, Benkovic SJ, Hammes GG
Journal:Biochemistry
PubMed ID:16800624
'In T4 bacteriophage, the DNA polymerase holoenzyme is responsible for accurate and processive DNA synthesis. The holoenzyme consists of DNA polymerase gp43 and clamp protein gp45. To form a productive holoenzyme complex, clamp loader protein gp44/62 is required for the loading of gp45, along with MgATP, and also for the ... More
Assembly of the bacteriophage T4 primosome: single-molecule and ensemble studies.
Authors:Zhang Z, Spiering MM, Trakselis MA, Ishmael FT, Xi J, Benkovic SJ, Hammes GG
Journal:Proc Natl Acad Sci U S A
PubMed ID:15728347
'Within replisomes for DNA replication, the primosome is responsible for unwinding double-stranded DNA and synthesizing RNA primers. Assembly of the bacteriophage T4 primosome on individual molecules of ssDNA or forked DNA (fDNA) has been studied by using FRET microscopy. On either DNA substrate, an ordered process of assembly begins with ... More
Conformation coupled enzyme catalysis: single-molecule and transient kinetics investigation of dihydrofolate reductase.
Authors:Antikainen NM, Smiley RD, Benkovic SJ, Hammes GG
Journal:Biochemistry
PubMed ID:16363797
'Ensemble kinetics and single-molecule fluorescence microscopy were used to study conformational transitions associated with enzyme catalysis by dihydrofolate reductase (DHFR). The active site loop of DHFR was labeled with a fluorescence quencher, QSY35, at amino acid position 17, and the fluorescent probe, Alexa555, at amino acid 37, by introducing cysteines ... More
Four-color single-molecule fluorescence with noncovalent dye labeling to monitor dynamic multimolecular complexes.
Authors:DeRocco V, Anderson T, Piehler J, Erie DA, Weninger K,
Journal:Biotechniques
PubMed ID:21091445
To enable studies of conformational changes within multimolecular complexes, we present a simultaneous, four-color single molecule fluorescence methodology implemented with total internal reflection illumination and camera-based, wide-field detection. We further demonstrate labeling histidine-tagged proteins noncovalently with Tris-nitrilotriacetic acid (Tris-NTA)-conjugated dyes to achieve single molecule detection. We combine these methods to ... More
Organization of the archaeal MCM complex on DNA and implications for the helicase mechanism.
Authors:McGeoch AT, Trakselis MA, Laskey RA, Bell SD
Journal:Nat Struct Mol Biol
PubMed ID:16116441
The homomultimeric archaeal mini-chromosome maintenance (MCM) complex serves as a simple model for the analogous heterohexameric eukaryotic complex. Here we investigate the organization and orientation of the MCM complex of the hyperthermophilic archaeon Sulfolobus solfataricus (Sso) on model DNA substrates. Sso MCM binds as a hexamer and slides on the ... More