产品
编 号：F749570
分子式：C16H19BF2N2O2
分子量：320.14
分子式：C16H19BF2N2O2
分子量：320.14
产品类型
规格
价格
是否有货
1mg
询价
询价
5mg
询价
询价
10mg
询价
询价
结构图
CAS No: 217075-24-6
产品详情
生物活性：
BODIPY FL C5 is a green fluorescent fatty acid. BODIPY FL C5 can be used as a precursor for the synthesis of various fluorescent phospholipids. BODIPY FL C5 is relatively insensitive to the environment and fluoresces in both water-soluble and lipid environments.
体外研究：
Guidelines (Following is our recommended protocol. This protocol only provides a guideline, and should be modified according to your specific needs).A. Enzyme assays:1. An aliquot of phospholipid was placed in a 1×1-cm fluorescence cuvette and buffer (50 mM Tris, pH 8, 100 mM NaCl, 1 mM CaCl2) was added to a total volume of 1.3 mL. The temperature was allowed to equilibrate at 35°C with stirring for several minutes and the background emission was recorded (the background rate was undetectable). Enzyme (1-10 μL) was added and the emission was recorded.2. An aliquot of phospholipid (78 μL of 0.05 mM substrate/0.5 mM DTPM) was placed in a 1×1-cm fluorescence cuvette and buffer (50 mM Tris, pH 8, 100 mM NaCl, 1 mM CaCl2, 30% glycerol) was added to a total volume of 1.3 mL. The temperature was allowed to equilibrate at 35°C with stirring for several minutes and the background emission was recorded (the background rate was undetectable). Enzyme (1-10 μL) was added with extra mixing of the viscous solution, andthe emission was recorded.3. A measured amount of BODIPYFL-C5 (in the case of PBPEC6DNP and MBPEDNP) or BODIPY-FL-C5-lyso-PAF (in the case of BC11-DNPC8-PC) was added to the phospholipid substrate solutions and the increase in emission was recorded. The factor, picomoles of BODIPY product/intensity unit increase, was then used to convert emission increase/sec to picomoles of product/second in the assays.B. Zebrafish in vitro assay:1. Embryoswere placed in 0.15 mL of embryo medium (EM: 13.7mM NaCl, 0.537 mM KCl, 0.025 mM Na2HPO4, 0.044mM KH2PO4, 1.30 mM CaCl2, 1 mM MgSO4, 4.2 mMNaHCO3, pH 7.2) .2. Containing 150-200 ng of a fluorescent phospholipid substrate, and sonicated for 2-5 s.3. After 1 h at 37℃, reactions were stopped by the addition of 0.45 mL of chloroform: methanol (2:1),mixed, and centrifuged (30 s, 16,000g) .4. The aqueous fraction was discarded and an aliquot of organic fraction was loaded on thin-layer chromatography plates. 5. Plates were developed in toluene: diethyl ether: ethanol: acetic acid (50:40:2:0.2) and quantified using a laser scanner.
BODIPY FL C5 is a green fluorescent fatty acid. BODIPY FL C5 can be used as a precursor for the synthesis of various fluorescent phospholipids. BODIPY FL C5 is relatively insensitive to the environment and fluoresces in both water-soluble and lipid environments.
体外研究：
Guidelines (Following is our recommended protocol. This protocol only provides a guideline, and should be modified according to your specific needs).A. Enzyme assays:1. An aliquot of phospholipid was placed in a 1×1-cm fluorescence cuvette and buffer (50 mM Tris, pH 8, 100 mM NaCl, 1 mM CaCl2) was added to a total volume of 1.3 mL. The temperature was allowed to equilibrate at 35°C with stirring for several minutes and the background emission was recorded (the background rate was undetectable). Enzyme (1-10 μL) was added and the emission was recorded.2. An aliquot of phospholipid (78 μL of 0.05 mM substrate/0.5 mM DTPM) was placed in a 1×1-cm fluorescence cuvette and buffer (50 mM Tris, pH 8, 100 mM NaCl, 1 mM CaCl2, 30% glycerol) was added to a total volume of 1.3 mL. The temperature was allowed to equilibrate at 35°C with stirring for several minutes and the background emission was recorded (the background rate was undetectable). Enzyme (1-10 μL) was added with extra mixing of the viscous solution, andthe emission was recorded.3. A measured amount of BODIPYFL-C5 (in the case of PBPEC6DNP and MBPEDNP) or BODIPY-FL-C5-lyso-PAF (in the case of BC11-DNPC8-PC) was added to the phospholipid substrate solutions and the increase in emission was recorded. The factor, picomoles of BODIPY product/intensity unit increase, was then used to convert emission increase/sec to picomoles of product/second in the assays.B. Zebrafish in vitro assay:1. Embryoswere placed in 0.15 mL of embryo medium (EM: 13.7mM NaCl, 0.537 mM KCl, 0.025 mM Na2HPO4, 0.044mM KH2PO4, 1.30 mM CaCl2, 1 mM MgSO4, 4.2 mMNaHCO3, pH 7.2) .2. Containing 150-200 ng of a fluorescent phospholipid substrate, and sonicated for 2-5 s.3. After 1 h at 37℃, reactions were stopped by the addition of 0.45 mL of chloroform: methanol (2:1),mixed, and centrifuged (30 s, 16,000g) .4. The aqueous fraction was discarded and an aliquot of organic fraction was loaded on thin-layer chromatography plates. 5. Plates were developed in toluene: diethyl ether: ethanol: acetic acid (50:40:2:0.2) and quantified using a laser scanner.
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