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ABD-F

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Item #	Description/Size	Availability	Qty Break	Price	Quantity
A016-10	50 mg	5-10 business days	1	$195.00
A016-12	100 mg	5-10 business days	1	$309.00

*Estimated. Exact shipping date will be notified.
For Research Use Only Products

Application: Thiol compound derivatization for HPLC analysis

Description
Application

Chemical Name: 4-Fluoro-7-sulfamoylbenzofurazan
CAS: 91366-65-3

Appearance: White or slightly yellow crystalline powder
Purity: ≥99.0% (HPLC)
MW: 217.18, C₆H₄FN₃O₃S

Storage Condition: -20ºC, protect from light and moisture
Shipping Condition: ambient temperature

Derivatization Reaction

Product Description
ABD-F has a benzofurazan moiety that produces a highly fluorescent compound through the reaction with a sulfhydryl group. The excitation and emission of the devivatized compound are 389 nm and 513 nm, respectively. The reaction rate of ABD-F is 30 times faster than that of SBD-F. ABD-F reactions with thiol compounds are completed within 5 minutes in aqueous conditions at 50ºC, pH 8. However, ABD-F does not react with alanine, proline, or cysteine under these conditions. Its maximum fluorescence intensity can be observed at pH 2. In reversephase HPLC analysis, pre-labeled ABD-thiol compounds can be detected separately. The detection limits (S/N=3) are 0.6 pmol per injection for cysteine, 0.4 pmol per injection for glutathione, 1.9 pmol per injection for N-acetylcysteine, and 0.5 pmol per injection for cysteamine.

ABD Labeling Protocol
1. To prepare sample solution, mix or dissolve a sample with 100 mM borate buffer, pH 8.0 containing 2 mM EDTA.
2. Mix 500 μl of the sample solution and 500 μl of 1 mM ABD-F/100 mM borate buffer in a reaction vial.
3. Heat the vial at 50ºC for 5 minutes and cool it on an ice bath.
4. Add 300 μl of 100 mM HCl aqueous solution to the reaction mixture.
5. Use this mixture for HPLC analysis to determine ABD-labeled compounds; excitation: 389 nm, emission: 513 nm.

References
1. T. Toyo’oka, et al., New Fluorogenic Reagent Having Halogenobenzofurazan Structure for Thiols: 4-(Aminosulfonyl)-7-fluoro-2, 1, 3-benzoxadiazole. Anal Chem. 1984;56:2461-2464.
2. T. Toyo’oka, et al., Isolation and Characterization of Cysteine-Containing Regions of Proteins Using 4-(Aminosulfonyl)-7-fluoro-2, 1, 3-benzoxadiazole and High-Performance Liquid Chromatography. Anal Chem. 1985;57:1931-1937.
3. T. Toyo’oka, et al., Amino Acid Composition Analysis of Minute Amounts of Cysteine-containing Proteins Using 4-(Aminosulfonyl)-7-fluoro-2, 1, 3-benzoxadiazole and 4-fluoro-7-nitro-2, 1, 3-benzoxadiazole in Combination with HPLC. Biomed Chromatogr. 1986;1:15-20.
4. T. Toyo’oka, et al., Simultaneous Determination of Thiols and Disulfides by High-performance Liquid Chromatography with Fluorescence Detection. Anal Chim Acta. 1988;205:29-41.
5. Y. Luo, et al., Antichymotrypsin interaction with chymotrypsin. Intermediates on the way to inhibited complex formation. J Biol Chem. 1999;274:17733-17741.