| 货号 (SKU) | 包装规格 | 是否现货 | 价格 | 数量 |
|---|---|---|---|---|
| A638805-1mg |
1mg |
期货  |
|
| 规格或纯度 | Ex:518nm, Em:543nm |
|---|---|
| 英文名称 | Aladdin Fluor 514 NHS Ester |
| 储存温度 | 避光,-20°C储存 |
| 运输条件 | 超低温冰袋运输 |
| 产品介绍 |
Alexa Fluor™ 514 is a bright, green-fluorescent dye. Used for stable signal generation in imaging and flow cytometry, Alexa Fluor™ 514 dye is water soluble and pH-insensitive from pH 4 to pH 10. In addition to reactive dye formulations, we offer Alexa Fluor™ 514 dye conjugated to a variety of antibodies, peptides, proteins, tracers, and amplification substrates optimized for cellular labeling and detection. The NHS ester (or succinimidyl ester) of Alexa Fluor™ 514 is the most popular tool for conjugating this dye to a protein or antibody. NHS esters can be used to label to the primary amines (R-NH2) of proteins, amine-modified oligonucleotides, and other amine-containing molecules. The resulting Alexa Fluor™ conjugate will exhibit brighter fluorescence and greater photostability than the conjugates of other spectrally similar fluorophores. Detailed information about this Aladdin Fluor NHS ester: Fluorophore label: Alexa Fluor™ 514 dye Reactive group: NHS ester Reactivity: Primary amines on proteins and ligands, amine-modified oligonucleotides Ex/Em of the conjugate: 517/542 nm Extinction coefficient: 80,000 cm-1M-2 Typical Conjugation Reaction You can conjugate amine-reactive reagents with virtually any protein or peptide (the provided protocol is optimized for IgG antibodies). You can scale the reaction for any amount of protein, but the concentration of the protein should be at least 2 mg/mL for optimal results. We recommend trying three different degrees of labeling, using three different molar ratios of the reactive reagent to protein. The Alexa Fluor™ NHS ester is typically dissolved in high-quality anhydrous dimethylformamide (DMF) or dimethylsulfoxide (DMSO) , and the reaction is carried out in 0.1–0.2 M sodium bicarbonate buffer, pH 8.3, at room temperature for 1 hour. Because the pKa of the terminal amine is lower than that of the lysine epsilon-amino group, you may achieve more selective labeling of the amine terminus using a buffer closer to neutral pH. 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 () Antibody Conjugate Purification Kit for 20-50 µg () Antibody Conjugate Purification kit for 50-100 µg () We offer a wide selection of Molecular Probes™ antibody and protein labeling kits to fit your starting material and your experimental setup. See ourAntibody Labeling kits or use ourKits for Labeling Proteins and Nucleic Acids—Section 1.2 in The Molecular Probes™ Handbook. 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. Ourcustom conjugation service is efficient and confidential, and we stand by the quality of our work. We are ISO 9001:2000 certified. |
| Reactivity | Amine |
|---|
| Excitation(nm) | 517 |
|---|---|
| Emission(nm) | 542 |
| 1. Hausmann M, Winkler R, Hildenbrand G, Finsterle J, Weisel A, Rapp A, Schmitt E, Janz S, Cremer C. COMBO-FISH: specific labeling of nondenatured chromatin targets by computer-selected DNA oligonucleotide probe combinations.. Biotechniques, [PMID:14513562] |
| 2. Kravchenko-Balasha N,Wang J,Remacle F,Levine RD,Heath JR. Glioblastoma cellular architectures are predicted through the characterization of two-cell interactions.. [PMID:24733941] |
| 3. Alford R, Simpson HM, Duberman J, Hill GC, Ogawa M, Regino C, Kobayashi H, Choyke PL,. Toxicity of organic fluorophores used in molecular imaging: literature review.. Mol Imaging, [PMID:20003892] |
| 4. Rolain T,Bernard E,Beaussart A,Degand H,Courtin P,Egge-Jacobsen W,Bron PA,Morsomme P,Kleerebezem M,Chapot-Chartier MP,Dufrêne YF,Hols P. O-glycosylation as a novel control mechanism of peptidoglycan hydrolase activity.. [PMID:23760506] |
| 5. Choi HM, Chang JY, Trinh le A, Padilla JE, Fraser SE, Pierce NA,. Programmable in situ amplification for multiplexed imaging of mRNA expression.. Nat Biotechnol, [PMID:21037591] |
| 6. Tadross MR, Park SA, Veeramani B, Yue DT,. Robust approaches to quantitative ratiometric FRET imaging of CFP/YFP fluorophores under confocal microscopy.. J Microsc, [PMID:19196425] |
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