saRNA经工程化改造,可实现萤火虫荧光素酶的持续且扩增型表达。荧光素酶最初从萤火虫(Photinus pyralis)中提取,能够催化荧光素氧化生成氧化荧光素,并发出黄绿色生物荧光(波长550–570 nm),其荧光强度可直接反映荧光素酶的表达水平。与常规mRNA 不同,saRNA兼具mRNA编码能力与内源自复制机制,从而实现荧光素酶的持续表达。
・saRNA 转染阳性对照:验证转染效率与体系性能
・递送系统筛选:评估saRNA-LNP 制剂的递送应用效果
9449 nt
1 mg/mL
1 mM sodium citrate, pH 6.5
-65℃以下
干冰运输
目视法
USP<791>
紫外分光光度法
紫外分光光度法
高效液相色谱法
毛细管电泳法
荧光染料法
酶联免疫吸附法
实时荧光定量PCR法
凝胶法

Figure 1. The saRNA samples were delivered into 293T cells using a transfection reagent at doses ranging from 0.781 to 12.5 ng per well. 48 hours post-transfection, firefly luciferase (FLuc) activity was measured by adding the D-luciferin substrate and recording luminescence with a microplate reader. The observed luminescence confirmed that FLuc protein was successfully expressed in the transfected cells.