Alexa Fluor™ 350 C5 Maleimide
Alexa Fluor&trade; 350 C<sub>5</sub> Maleimide
Invitrogen™

Alexa Fluor™ 350 C5 Maleimide

Alexa Fluor™ 350 is a blue fluorescent dye with moderate photostability and excitation that matches the 350 nm laser line.자세히 알아보기
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카탈로그 번호수량
A305051 mg
카탈로그 번호 A30505
제품 가격(KRW)
500,000
Online offer
Ends: 31-Dec-2025
624,000
할인액 124,000 (20%)
Each
카트에 추가하기
수량:
1 mg
제품 가격(KRW)
500,000
Online offer
Ends: 31-Dec-2025
624,000
할인액 124,000 (20%)
Each
카트에 추가하기
Alexa Fluor™ 350 is a blue fluorescent dye with moderate photostability and excitation that matches the 350 nm laser line. Used for stable signal generation in imaging and flow cytometry, Alexa Fluor™ 350 dye is water soluble and pH-insensitive from pH 4 to pH 10. In addition to reactive dye formulations, we offer Alexa Fluor™ 350 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™ 350 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™ 350 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™ 350 dye
Reactive group: maleimide
Reactivity: thiol groups on proteins and ligands, oligonucleotide thiophosphates
Ex/Em of the conjugate: 345/444 nm
Extinction coefficient: 17,000 cm-1M-1
Spectrally similar dyes: Marina Blue
Molecular weight: 578.68

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.
사양
화학물질 반응성Thiol
방출444 nm
여기345 nm
라벨 또는 염료Alexa Fluor™ 350
제품 유형Dye
수량1 mg
반응성 부분Maleimide
배송 조건Room Temperature
라벨 유형Alexa Fluor
제품라인Alexa Fluor
Unit SizeEach
구성 및 보관
Store in freezer (-5 to -30°C) and protect from light.

자주 묻는 질문(FAQ)

What are the signal intensity differences between Alexa Fluor 350 dye and Alexa Fluor 488 dye?

In general, blue fluorescent dyes are not as bright as other dyes further along the color spectrum. Blue dyes are structurally smaller and have lower extinction coefficients, so they are typically not as bright compared to the green, red, and far red dyes.
When using an Alexa Fluor 350 secondary antibody, we recommend that you use it for highly expressed targets and at a higher concentration than what is typically required for green or red secondary antibodies.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

인용 및 참조 문헌 (5)

인용 및 참조 문헌
Abstract
The structure of calreticulin C-terminal domain is modulated by physiological variations of calcium concentration.
Authors:Villamil Giraldo AM, Lopez Medus M, Gonzalez Lebrero M, Pagano RS, Labriola CA, Landolfo L, Delfino JM, Parodi AJ, Caramelo JJ,
Journal:J Biol Chem
PubMed ID:20018892
Calreticulin is an abundant endoplasmic reticulum resident protein that fulfills at least two basic functions. Firstly, due to its ability to bind monoglucosylated high mannose oligosaccharides, calreticulin is a central component of the folding quality control system of glycoproteins. On the other hand, thanks to its capacity to bind high ... More
A method for site-specific labeling of multiple protein thiols.
Authors:Kuiper JM, Pluta R, Huibers WH, Fusetti F, Geertsma ER, Poolman B,
Journal:Protein Sci
PubMed ID:19388048
'We present a generic method for the site-specific and differential labeling of multiple cysteine residues in one protein. Phenyl arsenic oxide has been employed as a protecting group of two closely spaced thiols, allowing first labeling of a single thiol. Subsequently, the protecting group is removed, making available a reactive ... More
Domains II and III of Bacillus thuringiensis Cry1Ab toxin remain exposed to the solvent after insertion of part of domain I into the membrane.
Authors:Zavala LE, Pardo-López L, Cantón PE, Gómez I, Soberón M, Bravo A,
Journal:J Biol Chem
PubMed ID:21464133
Bacillus thuringiensis produces insecticidal proteins named Cry toxins, that are used commercially for the control of economical important insect pests. These are pore-forming toxins that interact with different receptors in the insect gut, forming pores in the apical membrane causing cell burst and insect death. Elucidation of the structure of ... More
An eight residue fragment of an acyl carrier protein suffices for post-translational introduction of fluorescent pantetheinyl arms in protein modification in vitro and in vivo.
Authors:Zhou Z, Koglin A, Wang Y, McMahon AP, Walsh CT,
Journal:J Am Chem Soc
PubMed ID:18593165
Genetically encoded tags for tracking a given protein continue to be of great interest in a multitude of in vitro and in vivo contexts. Acyl carrier proteins, both free-standing and as embedded 80-100 residue domains, contain a specific serine side chain that undergoes post-translational pantetheinylation from CoASH as donor substrate. ... More
Efficiencies of fluorescence resonance energy transfer and contact-mediated quenching in oligonucleotide probes.
Authors:Marras SA, Kramer FR, Tyagi S
Journal:Nucleic Acids Res
PubMed ID:12409481
An important consideration in the design of oligonucleotide probes for homogeneous hybridization assays is the efficiency of energy transfer between the fluorophore and quencher used to label the probes. We have determined the efficiency of energy transfer for a large number of combinations of commonly used fluorophores and quenchers. We ... More