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            當前位置: 首頁> 產品中心> 細胞生物學 > 熒光探針與細胞染色 > MKBio BMPO (Spin trapping reagent) 自旋捕獲劑
            MKBio BMPO (Spin trapping reagent) 自旋捕獲劑
            目錄號 MX4722-5MG 售價 1646.00元
            規格 5mg 運輸溫度 冰袋運輸。
            其他名稱 5-tert-butoxycarbonyl 5-methyl-1-pyrroline N-oxide; BocMPO; 保存溫度 -20℃避光干燥保存,2年有效
            CAS號 387334-31-8 有效期 2年
            應用 自旋捕獲劑 訂購數量
            產品簡介:

            BMPO (Spin trapping reagent)自旋捕獲劑


            產品標簽

            BMPO;DEPMPO;EMPO;Spin trapping reagent自旋捕獲劑;電子順磁共振波譜(EPR);CAS: 387334-31-8;


            產品信息

            產品名稱

            產品編號

            CAS NO.            

            規格         

            價格(元)   

            BMPO (Spin trapping reagent)自旋捕獲劑

            MX4722-5MG

            387334-31-8

            5mg

            1646

            BMPO (Spin trapping reagent)自旋捕獲劑

            MX4722-10MG

            387334-31-8

            10mg

            2486

            BMPO (Spin trapping reagent)自旋捕獲劑

            MX4722-50MG

            387334-31-8

            50mg

            8236


            產品描述

            BMPO(5-tert-butoxycarbonyl 5-methyl-1-pyrroline N-oxide)是一種新型高效且高穩定型的硝酮自旋捕獲劑(Nitrone Spin Trapping Reagent),由美國威斯康星醫學院Kalyanaraman教授的實驗室團隊開發,非常適合用于特異性檢測和鑒定體內外形成的硫自由基、羥基自由基(?OH)和超氧陰離子自由基(?O2-),通過形成用電子順磁共振波譜(EPR)可區分的加合物來測定[1-2]。


            BMPO具有以下特點:

            ①特異性高,半衰期長:其它的硝酮自旋捕獲劑比如:DMPO,難以輕易區分超氧陰離子和羥基自由基,因產生的DMPO-超氧加合物(半衰期t?=45s)瞬間衰減產生DMPO-羥基加合物。與最近開發的自旋捕獲劑:DEPMPO和EMPO類似,BMPO-超氧加合物不會衰減生成羥基加合物,但是,BMPO-超氧加合物的半衰期最長(t?=23min)。

            ②產品穩定性高:DEPMPO和EMPO是液體自旋捕獲劑,通常被硝基氧雜質污染,且效期有限。BMPO是固體的環形硝酮,通過結晶以高度純化的狀態提供,能夠保存更長的周期,且不用擔心降解。

            ③更高的信噪比:BMPO衍生的加合物在各自的EPR光譜中具有更高的信噪比,使其更適合用于檢測細胞懸浮液中的亞硫酸、羥基和甲基自由基。

            ④高水溶性:水溶性好,更利于水相體系自由基的研究,尤其是生物體系的自由基研究。


            產品特性

            1) CAS NO:387334-31-8

            2) 化學名:3,4-dihydro-2-methyl-1,1-dimethylethyl ester-2H-pyrrole-2-carboxylic acid-1-oxide

            3) 同義名:5-tert-butoxycarbonyl 5-methyl-1-pyrroline N-oxide; BocMPO;

            4) 分子式:C10H17NO3

            5) 分子量:199.2

            6) 純度:≥98%

            7) 外觀:結晶或結晶性粉末

            8) 溶解性:溶于水、PBS(pH 7.2, 10mg/ml)、DMSO(25mg/ml)、無水乙醇(25mg/ml)

            8)化學結構式:

            保存與運輸方法

            保存:-20oC干燥保存,2年有效。 

            運輸:冰袋運輸。


            注意事項

            為了您的安全和健康,請穿實驗服并戴一次性手套操作。


            參考文獻

            1. Zhao, H., Joseph, J., Zhang, H., et al. Synthesis and biochemical applications of a solid cyclic nitrone spin trap: A relatively superior trap for detecting superoxide anions and glutathiyl radicals. Free Radic. Biol. Med. 31(5), 599-606 (2001).

            2. Khan, N., Wilmont, C.M., Rosen, G.M., et al. Spin traps: In vitro toxicity and stability of radical adducts. Free Radical Biology & Medicine 34(11), 1473-1481 (2003).


            應用示例(僅作參考)

            1.文獻來源:Mitchell DG, Rosen GM, Tseitlin M, Symmes B, Eaton SS, Eaton GR. Use of rapid-scan EPR to improve detection sensitivity for spin-trapped radicals. Biophys J. 2013 Jul 16;105(2):338-42. doi: 10.1016/j.bpj.2013.06.005. PMID: 23870255; PMCID: PMC3714875. Editedby MKBIO


            ①黃嘌呤-黃嘌呤氧化酶體系內超氧陰離子(O2??)生成的測定:Typically, xanthine oxidase (0.04 U/mL) was added to pH ~7.4 sodium phosphate buffer (50 mM) containing DTPA (1 mM) and hypoxanthine (0.5–400 μM, final concentration) to achieve rates of O2?? formation that ranged from 0.1 to 6.0 μM/min. We estimated the superoxide formation rate by monitoring the SOD-inhibitable reduction of ferricytochrome c (80 μM) at room temperature. Spin trapping was performed by addition of 100 mM BMPO in pH ~7.4 phosphate-buffered saline (PBS; 50 mM) containing 1 mM DTPA to the solution of hypoxanthine and xanthine oxidase to achieve a final BMPO concentration of 50 mM in the reaction mixture. EPR spectra were recorded 10 min after mixing reagents. The half-life of BMPO-OOH at ambient temperature is reported to be ~23 min. Solutions for control experiments contained SOD (30 U/mL).

            Figure 2 Comparison of CW and rapid-scan spectra of BMPO-OOH in solution with a O2?? production rate of 0.1μM/min, recorded 10 min after mixing reagents. The O2?? was produced by a hypoxanthine/xanthine oxidase mixture. The concentration of BMPO-OOH is ~0.3μM. (A) CW spectrum obtained with 55 G sweep width, 0.75 G modulation amplitude, single 30 s scan, 15 ms conversion time, 10 ms time constant, and 20 mW (B1 = 170 mG) microwave power. (B) Deconvolved rapid-scan spectrum obtained with 55 G scan width, 51 kHz scan frequency, and 53 mW (B1 = 250 mG) microwave power. Segments consisting of 12 sinusoidal cycles were averaged 100 k times, with a total data acquisition time of ~30 s.


            2.文獻來源:Wang, Z., Zhang, Y., Ju, E.et al. Biomimetic nanoflowers by self-assembly of nanozymes to induce intracellular oxidative damage against hypoxic tumors.Nat Commun 9,3334 (2018). https://doi.org/10.1038/s41467-018-05798-x 

            ①缺氧下的ESR測定(O2??,?OH):For O2?? detection, the pre-deoxidized PBS (pH 5.0, 25?mM) contained 25?mM BMPO, 20?μg?mL?1 MnO2@PtCo nanoflowers, 100?μM H2O2, 50% DMSO was prepared. After incubation of 5?min, ESR spectra were recorded. For ?OH detection, the pre-deoxidized PBS (pH 5.0, 25?mM) contained 25?mM BMPO, 20?μg?mL?1 MnO2@PtCo nanoflowers, 100?μM H2O2, 0.25?U?mL?1 SOD was prepared. After incubation of 5?min, ESR spectra were recorded. The following instrument settings were used for collecting ESR spectra: 1?G field modulation, 100?G scan range, and 20?mW microwave power.

            Fig f ESR spectra of BMPO/?OOH adducts from different groups in the hypoxic H2O2 (100?μM) condition upon addition of DMSO.g ESR spectra of BMPO/?OH adducts were collected from different samples in the hypoxic H2O2 (100?μM) condition upon addition of SOD. Data were presented as mean?±?s.d. (n=?5).


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