Rhod-2, AM, cell permeant - Special Packaging

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Rhod-2, AM, cell permeant - Special Packaging

货号:R1244,R1245MP

规格:1 mg,20 x 50 µg

价格:7775,8580

产品类型:细胞凋亡检测

品牌:Thermo Fisher

物种:恒河猴/小鼠/大鼠

宿主:小鼠

抗体亚型:IgG

荧光染料:eFluor 506

标记的钙指示剂是结合 Ca2+后显示荧光增加的分子。它们可用于多种钙信号传导研究,包括自发荧光水平很高的细胞和组织中 Ca2+的测量以及光感受器和光活化螯合剂产生的 Ca2+释放的检测。将溶解后的指示剂直接加入含有培养细胞的培养皿中,即可向细胞上样 AM 酯形式的这类钙离子指示剂。通常使用荧光显微镜检测这些细胞的荧光信号。钙指示剂(AM 酯)规范:•标签(Ca2+– 结合形式的激发/发射波长):Rhod-2 (552/581 nm)• 结合 Ca2+后荧光强度增加:>100 倍•缓冲液中无 Mg2+时 Ca2+的 Kd:∼570 nM• 结合 Ca2+后,荧光增加,波长稍有变化使用 TPEN 控制重金属阳离子此外,基于 BAPTA 的指示剂可结合各种重金属阳离子(例如 Mn2+、Zn2+、Pb+2),亲和力远高于 Ca2+。由于存在这些离子而引起的钙测量的扰动可以使用重金属选择性螯合剂TPEN进行控制。钙荧光指示剂的更多选择我们提供了大量 Molecular Probes™ 钙指示剂,可用于各种实验方案,例如右旋糖酐形式可减少泄漏和区室化、BAPTA 偶联物用于检测高幅钙瞬变。有关更多信息,请查看 Molecular Probes™ 手册中的使用可见光激发的荧光 Ca2+指示剂—第 19.3 节。对于 UV 激发的 Ca2+指示剂、基于蛋白的 Ca2+指示剂、Ca2+指示剂的偶联物以及其他金属离子(即 Mg2+、Zn2+)的荧光指示剂,请查看 Molecular Probes™ 手册中的Ca2+、Mg2+、Zn2+以及其他金属离子指示剂—第 19 章。仅供科研使用。不可用于人或动物的治疗或诊断。

数据:
图1.Metal-ion response screening for rhod-2.Metal-ion response screening for rhod-2 (Cat. no. R1244, R1245MP, R14220). The maximum relative fluorescence intensity was measured for identical indicator concentrations in solutions containing 10 mM EGTA + 10 µM TPEN, 1 µM ion (100 µM for Mg2+) and 100 µM ion (10 mM for Mg2+). Results are plotted as fluorescence changes relative to the ion-free (10 mM EGTA + 10 µM TPEN) reference solution expressed as (F-Fo)/Fo, where F is the fluorescence intensity of ion-containing solutions and Fo is the fluorescence intensity of the reference solution. Blue bars indicate the response to 1 µM ion (100 µM for Mg2+), and red bars indicate the response to 100 µM ion (10 mM for Mg2+).

图2.Adult rat cortical astrocyte. Rhod-2 AM and MitoFluor™ Green stain.Colocalization of fluorescent staining by rhod-2 AM (Cat. no. R1244, R1245MP; upper panel) and mitochondrion-selective MitoFluor™ Green stain (Cat. no. M7502; lower panel) in an adult rat cortical astrocyte. Cells were simultaneously loaded with rhod-2 AM (4.5 µM) and the MitoFluor™ Green stain (20 nM) for 30 minutes at 22°C. Confocal laser-scanning microscopy using 488 nm excitation and spectrally resolved detection, at 505–530 nm for MitoFluor™ Green stain and >=585 nm for rhod-2, shows almost identical staining distribution. The images were contributed by Michael Duchen, University College, London. Reproduced with permission from J Cell Biol 145, 795 (1999).

图3.Colocalization of fluorescent staining by rhod-2 AM and mitochondrion-selective MitoFluor™ Green stain in an adult rat cortical astrocyte.Colocalization of fluorescent staining by rhod-2 AM (Cat. no. R1244, R1245MP; upper panel) and mitochondrion-selective MitoFluor™ Green stain (Cat. no. M7502; lower panel) in an adult rat cortical astrocyte. Cells were simultaneously loaded with rhod-2 AM (4.5 µM) and the MitoFluor™ Green stain (20 nM) for 30 minutes at 22°C. Confocal laser-scanning microscopy using 488 nm excitation and spectrally resolved detection, at 505–530 nm for MitoFluor™ Green stain and =585 nm for rhod-2, shows almost identical staining distribution. The images were contributed by Michael Duchen, University College, London. Reproduced with permission from J Cell Biol 145, 795 (1999).

相关产品:
▪细胞周期检测▪细胞凋亡检测▪细胞增殖活性检测

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