keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Janelia Fluor 669, SE (JF669, SE), a red fluorescent dye, can be directly reacted with the available thiol-containing HaloTag ligand under mild conditions (DIEA, DMF) to afford a JF669 HaloTag ligand in a single step (Ex = 669 nm; Em = 682 nm).
产品描述 | Janelia Fluor 669, SE (JF669, SE), a red fluorescent dye, can be directly reacted with the available thiol-containing HaloTag ligand under mild conditions (DIEA, DMF) to afford a JF669 HaloTag ligand in a single step (Ex = 669 nm; Em = 682 nm). |
体外活性 |
JF669 undergoes rapid conversion to thioether product (<5 min to completion) in organic solvents, where the dye predominantly adopts the closed form[1]. JF669 displays comparatively excellent photostability, retaining 97% fluorescence after the same number of cycles[1]. |
别名 | JF669, SE, JF669,NHS, Janelia Fluor? 669, SE |
分子量 | 693.77 |
分子式 | C34H30F3N3O6SSi |
CAS No. | 2127150-20-1 |
keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year
对于不同动物的给药剂量换算,您也可以参考 更多...
请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法: 比如您的给药剂量是10 mg/kg,每只动物体重20 g,给药体积100 μL,一共给药动物10 只,您使用的配方为5% DMSO+30% PEG300+5% Tween 80+60% ddH2O。那么您的工作液浓度为2 mg/mL。
母液配置方法:2 mg 药物溶于 50 μL DMSO (母液浓度为 40 mg/mL), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。
您可能有的问题的答案可以在抑制剂处理说明中找到,包括如何准备库存溶液,如何存储产品,以及基于细胞的分析和动物实验需要特别注意的问题。
Janelia Fluor® 669, SE 2127150-20-1 JF669, SE JF669,NHS Janelia Fluor? 669, SE Inhibitor inhibitor inhibit