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BODIPY™ 630/650-X NHS Ester(Succinimidyl Ester) , CAS No.B638879

Item Number
B638879
Grouped product items
SKUSizeAvailabilityPrice Qty
B638879-5mg
5mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$926.90

Basic Description

Storage TempProtected from light,Store at -20°C
Shipped InIce chest + Ice pads
Product Description

Product introduction:

BODIPY™ 630/650-X dye is bright, far-red fluorescent dye. It has a high extinction coefficient and fluorescence quantum yield and is relatively insensitive to solvent polarity and pH change. In contrast to the highly water soluble fluorophores Alexa Fluor™ 488 dye and fluorescein (FITC), BODIPY™ dyes have unique hydrophobic properties ideal for staining lipids, membranes, and other lipophilic compounds. BODIPY™ 630/650-X dye has a relatively long excited-state lifetime (typically 5 nanoseconds or longer), which is useful for fluorescence polarization-based assays and a large two-photon cross-section for multiphoton excitation. In addition to reactive dye formulations, we offer BODIPY™ 630/650-X 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 BODIPY™ 630/650-X is the most popular tool for conjugating the dye to a protein or antibody. NHS esters can be used to label the primary amines (R-NH2) of proteins, amine-modified oligonucleotides, and other amine-containing molecules. The resulting BODIPY™ 630/650-X conjugates exhibit bright fluorescence, narrow emission bandwidths, and relatively long excited-state lifetimes, which can be useful for fluorescence polarization assays and two-photon excitation (TPE) microscopy.

This reactive dye contains a seven-atom aminohexanoyl ('X') spacer between the fluorophore and the NHS ester group. This spacer helps to separate the fluorophore from its point of attachment, potentially reducing the interaction of the fluorophore with the biomolecule to which it is conjugated.

Detailed information about this BODIPY™ 630/650-X NHS ester:

Fluorophore label: BODIPY™ 630/650-X dye
Reactive group: NHS ester (succinimidyl ester)
Reactivity: Primary amines on proteins and ligands, amine-modified oligonucleotides
Ex/Em of the conjugate: 625/640 nm
Extinction coefficient: 101,000 cm-1M-1
Molecular weight: 660.5

Typical Conjugation Reaction
Amine-reactive reagents can be conjugated with virtually any protein or peptide; the provided protocol is optimized for IgG antibodies. The reaction can be scaled 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 BODIPY™ 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 BODIPY™ 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 medium 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 ()

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 ourAntibody Labeling kits or use ourKits 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. Ourcustom conjugation service is efficient and confidential, and we stand by the quality of our work. We are ISO 9001:2000 certified.

Product Properties

ReactivityAmine

Certificates

Certificate of Analysis(COA)

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Related Documents

References

1. Brecher ME, Wong EC, Chen SE, Vampola C, Rocco RM.  ()  Antibiotic-labeled probes and microvolume fluorimetry for the rapid detection of bacterial contamination in platelet components: a preliminary report..  Transfusion,      [PMID:10773051]
2. Buschmann V, Weston KD, Sauer M.  ()  Spectroscopic study and evaluation of red-absorbing fluorescent dyes..  Bioconjug Chem,      [PMID:12526709]
3. Nanthakumar A, Pon RT, Mazumder A, Yu S, Watson A.  ()  Solid-phase oligonucleotide synthesis and flow cytometric analysis with microspheres encoded with covalently attached fluorophores..  Bioconjug Chem,      [PMID:10725106]
4. Barsky V, Perov A, Tokalov S, Chudinov A, Kreindlin E, Sharonov A, Kotova E, Mirzabekov A.  ()  Fluorescence data analysis on gel-based biochips..  J Biomol Screen,      [PMID:12097187]
5. Seo TS, Bai X, Kim DH, Meng Q, Shi S, Ruparel H, Li Z, Turro NJ, Ju J.  ()  Four-color DNA sequencing by synthesis on a chip using photocleavable fluorescent nucleotides..  Proc Natl Acad Sci U S A,      [PMID:15829588]
6. Snyder DS, Garon CF.  ()  Decreased uptake of bodipy-labelled compounds in the presence of the nuclear stain, DRAQ5..  J Microsc,      [PMID:12950469]
7. Marmé N, Knemeyer JP, Sauer M, Wolfrum J.  ()  Inter- and intramolecular fluorescence quenching of organic dyes by tryptophan..  Bioconjug Chem,      [PMID:14624626]
8. Palo K, Brand L, Eggeling C, Jäger S, Kask P, Gall K.  ()  Fluorescence intensity and lifetime distribution analysis: toward higher accuracy in fluorescence fluctuation spectroscopy..  Biophys J,      [PMID:12124251]
9. Smolewski P, Grabarek J, Kamentsky LA, Darzynkiewicz Z.  ()  Bivariate analysis of cellular DNA versus RNA content by laser scanning cytometry using the product of signal subtraction (differential fluorescence) as a separate parameter..  Cytometry,      [PMID:11598949]
10. Briddon SJ, Middleton RJ, Yates AS, George MW, Kellam B, Hill SJ.  ()  Application of fluorescence correlation spectroscopy to the measurement of agonist binding to a G-protein coupled receptor at the single cell level..  Faraday Discuss,      [PMID:14992407]
11. Baker JG, Middleton R, Adams L, May LT, Briddon SJ, Kellam B, Hill SJ,.  ()  Influence of fluorophore and linker composition on the pharmacology of fluorescent adenosine A1 receptor ligands..  Br J Pharmacol,      [PMID:20105183]
12. Middleton RJ, Briddon SJ, Cordeaux Y, Yates AS, Dale CL, George MW, Baker JG, Hill SJ, Kellam B.  ()  New fluorescent adenosine A1-receptor agonists that allow quantification of ligand-receptor interactions in microdomains of single living cells..  J Med Chem,      [PMID:17249651]
13. Caumartin J, Favier B, Daouya M, Guillard C, Moreau P, Carosella ED, LeMaoult J.  ()  Trogocytosis-based generation of suppressive NK cells..  EMBO J,      [PMID:17318190]
14. Tian J, Avalos AM, Mao SY, Chen B, Senthil K, Wu H, Parroche P, Drabic S, Golenbock D, Sirois C, Hua J, An LL, Audoly L, La Rosa G, Bierhaus A, Naworth P, Marshak-Rothstein A, Crow MK, Fitzgerald KA, Latz E, Kiener PA, Coyle AJ.  ()  Toll-like receptor 9-dependent activation by DNA-containing immune complexes is mediated by HMGB1 and RAGE..  Nat Immunol,      [PMID:17417641]
15. Beatty KE, Tirrell DA,.  ()  Two-color labeling of temporally defined protein populations in mammalian cells..  Bioorg Med Chem Lett,      [PMID:18774715]
16. Murphy EA, Majeti BK, Barnes LA, Makale M, Weis SM, Lutu-Fuga K, Wrasidlo W, Cheresh DA,.  ()  Nanoparticle-mediated drug delivery to tumor vasculature suppresses metastasis..  Proc Natl Acad Sci U S A,      [PMID:18607000]
17. Pontow SE, Heyden NV, Wei S, Ratner L.  ()  Actin cytoskeletal reorganizations and coreceptor-mediated activation of rac during human immunodeficiency virus-induced cell fusion..  J Virol,      [PMID:15194790]
18. Briddon SJ, Middleton RJ, Cordeaux Y, Flavin FM, Weinstein JA, George MW, Kellam B, Hill SJ.  (2004)  Quantitative analysis of the formation and diffusion of A1-adenosine receptor-antagonist complexes in single living cells..  Proc Natl Acad Sci USA,  101  (13): (4673-8).  [PMID:15070776]

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