-SulfoBiotics- Sulfide dibimane

Biosulfur Analysis
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Product codeSB15 -SulfoBiotics- Sulfide dibimane
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CAS No.1392113-30-2
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Chemical nameBis(2,5,6-trimethylpyrazolo[1,2-a]pyrazole-1,7-dione-3-ylmethyl)sulfide
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MWC20H22N4O4S=414.48
Unit size | Price | Item Code |
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Discription
Recent years, hydrogen sulfide (H2S) has been shown to exhibit various physiological activities such as vasodilation, cytoprotection, insulin secretion, and neurotransmitter regulation. Further, it has been attracting attention as an important signaling molecule following nitric oxide (NO) and carbon monoxide (CO). Hydrogen sulfide, like NO and CO, is recognized as a gaseous molecule, however its pKa is about 7, and at physiological pH, about 80% of hydrogen sulfide exists in the form of hydrogen sulfide ion (HS-). In addition, hydrogen sulfide ions take on various bonding forms and structures in vivo, and the details of their mechanism of action are still unknown, and elucidation of the biological functions of sulfur, particularly hydrogen sulfide, is eagerly awaited.
Monobromobimane is a thiol-specific fluorescent labeling agent that produces two molecules of Bimane for each molecule of hydrogen sulfide (Sulfide dibimane). Sulfide dibimane can be separated by HPLC from bimane compounds in which monobromobimane reacts with thiol compounds such as glutathione and cysteine. In addition, since the generated compounds are fluorescent, high-sensitivity analysis by fluorescence detection is possible. Recently, a method that achieves even higher sensitivity and selectivity by using Sulfide dibimane (S34) in combination with a mass spectrometer (MS) has been reported, and this method is being established as a detailed analysis method not only for hydrogen sulfide but also for various biological substances with SH groups.
Developer | Dojindo Molecular Technologies, Inc. |
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Manual
References
1) G. L. Newton, R. Dorian and R. C. Fahey, Anal. Biochem., 1981, 114, 383.
2) E. A. Wintner, T. L. Deckwerth, W. Langston, A. Bengtsson, D. Leviten, P. Hill, M. A. Insko, R. Dumpit, E. Vanden
Ekart, C. F. Toombs and C. Szabo, Br. J. Pharmacology, 2010, 160, 941.
3) X. Shen, C. B. Pattillo, S. Pardue, S. C. Bir, R. Wang and C. G. Kevil, Free Radic. Biol. Med., 2011, 50, 1021.
4) M. Nishida, T. Sawa, N. Kitajima, K. Ono, H. Ihara, H. Motohashi, M. Yamamoto, M. Suematsu, H. Kurose,
A. vander Vliet, B. A. Freeman, T. Shibata, K. Uchida, Y. Kumagai and T. Akaike, Nat. Chem. Biol., 2012, 8, 714.
5) X. Shen, G. P. Kolluru, S. Yuan and C. Kevil, Methods Enzymol., 2015, 554, 31.
Q & A
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Q
Stability of Sulfide dibimane.
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A
Sulfide dibimane is unstable to light, so it should be stored in a light-shielded place after opening the aluminum lamination zip.
After dissolving in acetonitrile, keep the solution shielded from light by aluminum foil, etc., and use it for measurement within the same day.
The acetonitrile solution is stable for several hours in a light-shielded condition.
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Q
What concentration of Sulfide dibimane should be prepared?
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A
Add 100 µl of acetonitrile (for HPLC) per tube of the product and dissolve to obtain a concentration of 0.1 mmol/l.
Dilute this solution with an arbitrary amount of acetonitrile to prepare the Sulfide dibimane calibration solution.
For preparation method, please refer to the manual of this product.
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Q
Is there an expiration date?
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A
It is stable for six months after delivery in an unopened package.
Due to the charactor of this reagent, it cannot be stored after dissolution, so please use the solution within the same day after preparation
Handling and storage condition
Appearance: | Colorless to slightly yellow solid |
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Purity (HPLC): | ≧ 97.0 % |
Dye content: | 0.540~0.600 (370 nm) |
0-5°C, Protect from light |