Methods The cell-free system was prepared by ultracentrifugation of Xenopus eggs and activated by cytochrome C.

方法超速离心制非洲爪蟾卵无细胞系,用细胞色素C激活为系。

We separated the subfractions of LDL by precipitating method and density gradient ultracentrifugation, and identified the subfraction by electronphoresis and electron microscope.

通沉淀法分离LDL,然后经超速离心法分离其亚组分。

Methods The cell-free system was prepared by ultracentrifugation of Xenopus eggs and activated by cytochrome C.

方法超速离心制非洲爪蟾卵无细胞体系,用细胞色素C激活为凋亡体系。

We separated the subfractions of LDL by precipitating method and density gradient ultracentrifugation, and identified the subfraction by electronphoresis and electron microscope.

通过沉淀法分离LDL,然后经过超速离心法分离其亚组分。

Methods The cell-free system was prepared by ultracentrifugation of Xenopus eggs and activated by cytochrome C.

方法超速离心制非洲爪蟾卵无细胞体系,用细胞色素C激活为凋亡体系。

We separated the subfractions of LDL by precipitating method and density gradient ultracentrifugation, and identified the subfraction by electronphoresis and electron microscope.

通过沉法离LDL,然后经过超速离心法离其亚组。

Methods The cell-free system was prepared by ultracentrifugation of Xenopus eggs and activated by cytochrome C.

方法超速心制非洲爪蟾卵无细胞体系,用细胞色素C激活为凋亡体系。

We separated the subfractions of LDL by precipitating method and density gradient ultracentrifugation, and identified the subfraction by electronphoresis and electron microscope.

通过沉淀法分LDL,然后经过超速心法分组分。

Methods The cell-free system was prepared by ultracentrifugation of Xenopus eggs and activated by cytochrome C.

方法超制非洲爪蟾卵无细胞体系,用细胞色素C激活为凋亡体系。

We separated the subfractions of LDL by precipitating method and density gradient ultracentrifugation, and identified the subfraction by electronphoresis and electron microscope.

通过沉淀法分LDL,然后经过超法分其亚组分。

Methods The cell-free system was prepared by ultracentrifugation of Xenopus eggs and activated by cytochrome C.

方法超速离心制非洲爪蟾卵无细胞体系,用细胞色素C激活为凋亡体系。

We separated the subfractions of LDL by precipitating method and density gradient ultracentrifugation, and identified the subfraction by electronphoresis and electron microscope.

通过沉淀法分离LDL,然后经过超速离心法分离其亚组分。

Methods The cell-free system was prepared by ultracentrifugation of Xenopus eggs and activated by cytochrome C.

方法超速离爪蟾卵无细胞体系,用细胞色素C激活为凋亡体系。

We separated the subfractions of LDL by precipitating method and density gradient ultracentrifugation, and identified the subfraction by electronphoresis and electron microscope.

通过沉淀法分离LDL,然后经过超速离法分离其亚组分。

Methods The cell-free system was prepared by ultracentrifugation of Xenopus eggs and activated by cytochrome C.

方法超速离心制非洲爪蟾卵无细胞体系,用细胞色素C激活为凋亡体系。

We separated the subfractions of LDL by precipitating method and density gradient ultracentrifugation, and identified the subfraction by electronphoresis and electron microscope.

通过沉淀法分离LDL,然后经过超速离心法分离其亚组分。

Methods The cell-free system was prepared by ultracentrifugation of Xenopus eggs and activated by cytochrome C.

方法超速离心制非洲爪蟾卵无细胞体系,用细胞色素C激活为凋亡体系。

We separated the subfractions of LDL by precipitating method and density gradient ultracentrifugation, and identified the subfraction by electronphoresis and electron microscope.

通法分离LDL,然后经超速离心法分离其亚组分。