SBFI AM ( Na+ Indicator) 鈉離子指示探針
產品編號 | 產品名稱 | 包裝規(guī)格 | 價格 |
NBS7676-100ug | SBFI AM ( Na+ Indicator) 鈉離子指示探針 | 2x50ug | 2073 |
NBS7676-500ug | SBFI AM ( Na+ Indicator) 鈉離子指示探針 | 10x50ug | 6928 |
NBS7676-1000ug | SBFI AM ( Na+ Indicator) 鈉離子指示探針 | 20x50ug | 11940 |
NBS7676-1mg | SBFI AM ( Na+ Indicator) 鈉離子指示探針 | 1mg | 11123 |
【溫馨提示】:見我司整理的鈉離子載體/探針(Sodium ionophores/indicators)產品專題。
【務必注意】:初次使用離子探針的用戶,強烈建議配合:Pluronic F-127, Cell Culture Tested 細胞培養(yǎng)級(NBS2009-1g)一起使用,以提高探針的水溶性和胞內加載性。
產品簡介:
SBFI,英文全名Sodium-binding Benzofuran Isophthalate,一種Na+選擇性熒光指示劑,可用來預測純化線粒體Na+梯度,檢測胞內Na+水平,測定細胞Na+外流,以及與其他熒光指示劑聯合使用以分析Na+與Ca2+和Mg2+濃度、胞內pH和膜電位變化的相關性。雖然SBFI對Na+的選擇能力弱于Ca2+指示劑比如Fura-2,但在其他單價陽離子存在體系,SBFI足以檢測Na+的生理濃度。結合離子后的SBFI光譜反應可通過激發(fā)光比率測定來判定,其能與用相同光濾片和儀器檢測的探針Fura-2共同使用。
當體系內含生理濃度的K+/Na+(~135mM),SBFI對Na+的解離常數(Kd)為11.3mM;而不存在K+體系,對Na+的Kd為3.8mM。SBFI對Na+的選擇性比K+約強18倍。
本品為乙酰氧基甲基酯(Acetoxymethyl ester, AM ester)形式的SBFI,CAS NO:129423-53-6,具有細胞膜滲透性,只需簡單孵育即可進入細胞,常用加載濃度范圍5-10μM,加載時間40min-4h,根據具體的實驗要求和細胞類型來調整。
產品特性:
1)化學名:4,4’-[1,4,10-trioxa-7,13-diazacyclopentadecane-7,13-diylbis(5-methoxy-6,2-benzofurandiyl)]bis-1,3- benzenedicarboxylic acid 1,1’,3,3’-tetrakis[(acetyloxy)methyl] ester
2)同義名:Sodium-binding Benzofuran Isophthalate Acetoxymethyl ester
3)CAS NO:129423-53-6
4)分子式:C56H58N2O23
5)分子量:1127.07
6)純度:>90%(HPLC)
7)Ex/Em:340,380/500 nm
8)外觀:淺黃至暗黃至暗橙固體或油狀
9)溶解性:溶于DMSO(10mM)
保存條件:
-20℃避光干燥穩(wěn)定凍存2年。
注意事項:
1. SBFI AM易受潮,粉末需要干燥保存;需用無水DMSO溶解,配制儲存液(如10mM),置于-20℃干燥避光,小量分裝避免反復凍融,至少3個月穩(wěn)定。
2. 由于SBFI AM水溶性較差,可在實驗前與等體積Pluronic F-127(25% w/v)混合,以提高探針加載效率。
3. 為了您的安全和健康,請穿實驗服并戴一次性手套操作。
文獻引用:
[1] Tong W et al. Phthalocyanine functionalized poly(glycidyl methacrylate) nano-assemblies for photodynamic inactivation of bacteria. Biomater. Sci., 2019,7, 1905-1918
[2] Li R et al. Biofilm inhibition and mode of action of epigallocatechin gallate against Vibrio mimicus. Food Control, Volume 113, July 2020, 107148
Then PBFI probe was added and incubated at 37 °C for 90 min.The cells were washed, collected and resuspended with PBS buffer. Aliquots (100 μL) of bacterial suspension were transferred to a Corning 96 well black plate, and 100 μL of various concentrations of EGCG were dispensed in the microtiter plate wells.
[3] Liu Y, Zhen W, Wang Y, Song S, Zhang H. Na2S2O8 Nanoparticles Trigger Antitumor Immunotherapy through Reactive Oxygen Species Storm and Surge of Tumor Osmolarity. J Am Chem Soc. 2020 Dec 30;142(52):21751-21757. doi: 10.1021/jacs.0c09482. Epub 2020 Dec 18. PMID: 33337859.
4T1 cells were inoculated into glass bottom culture dishes for 24 h. Then, adding PNSO NPs medium solution (80 μg/mL) to continue co-culture for 4 h. The treated 4T1 cells were further incubated with 10μM Na+ indicator SBFI AM in 0.04% Pluronic F-127 and the fluorescence signal was measured by CLSM.
[4] Liang Z, Yang Y, Yu G, et al. Engineering aluminum hydroxyphosphate nanoparticles with well-controlled surface property to enhance humoral immune responses as vaccine adjuvants. Biomaterials. 2021 Jun;275:120960. DOI: 10.1016/j.biomaterials.2021.120960.
[5] BMDMs were treated with AAHPs (250 μg/mL) in the presence of LPS at 500 ng/mL for 5 h.Then PBFI AM was added to the cells at the concentration of 10 μM, and cells were incubated at 37 °C for 1h. Triton X-100 (0.2%) treated cells were used as controls. The fluorescence of PBFI AM was measured at the Ex/Em of 340/615 nm. The data were expressed as relative fluorescence intensity (RFI) defined as the fluorescence intensity of AAHPs-treated BMDMs normalized to the intensity of control cells.
[6] Jia Y, Yang B, Shi J, Fang D, Wang Z, Liu Y. Melatonin prevents conjugative transfer of plasmid-mediated antibiotic resistance genes by disrupting proton motive force. Pharmacol Res. 2022 Jan;175:105978. doi: 10.1016/j.phrs.2021.105978. Epub 2021 Nov 21. PMID: 34813930.
As for the detection of intracellular K + concentration, the PBFI-AM (K + indicator) fluorescence dye labeled cells (10 μM) in the presence of…..
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